ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ

Objective. To research the ability of fungi of the genus Penicillium, isolated from the histosphere of soybean plants, release phosphorus from mineral and organic phosphates, study their effect on the general phosphorus content in plant shoots. Methods. Microbiological (cultivation of the tested fun...

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Hauptverfasser: Шаховніна, О. О., Надкернична, О. В., Пищур, І. М.
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Agriciltural microbiology
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author Шаховніна, О. О.
Надкернична, О. В.
Пищур, І. М.
author_facet Шаховніна, О. О.
Надкернична, О. В.
Пищур, І. М.
author_institution_txt_mv [ { "author": "О. О. Шаховніна", "institution": "Інститут сільськогосподарської мікробіології та агропромислового виробництва НААН" }, { "author": "О. В. Надкернична", "institution": "Інститут сільськогосподарської мікробіології та агропромислового виробництва НААН" }, { "author": "І. М. Пищур", "institution": "Інститут сільськогосподарської мікробіології та агропромислового виробництва НААН" } ]
author_sort Шаховніна, О. О.
baseUrl_str https://smic.in.ua/index.php/journal/oai
collection OJS
datestamp_date 2026-07-22T10:10:52Z
description Objective. To research the ability of fungi of the genus Penicillium, isolated from the histosphere of soybean plants, release phosphorus from mineral and organic phosphates, study their effect on the general phosphorus content in plant shoots. Methods. Microbiological (cultivation of the tested fungi on Pikovska’s medium and its modifications, Czapek-Dox agar with tricalcium phosphate or phenolphthalein phosphate, wort agar), vegetation experiment (content determination of general phosphorus in the aboveground mass of soybean plants), statistical. Results. The use of three insoluble phosphates in Pikovska medium showed that the tested fungi dissolve to varying degrees Са3(РО4)2 and are unable to dissolve AlPO4 and FePO4. On the seventh day of cultivation, clearly visible zones of enlightenment were formed around the colonies of P. funiculosum 20312 and P. variabile 20173, with phosphate dissolution indexes of 1.17 and 1.18, respectively. When cultivating fungi on Pikovska medium with the addition of bromophenol blue dye in P. funiculosum 20312 and P. variabile 20173, the medium quickly changed colour from green to yellow, indicating the diffusion of organic acids produced by the fungi into the agar. Starting from the twelfth day of the experiment, the environment around the colonies of fungi P. glauco-lanosum 20401 also acquired a rich yellow colour and the halo zones formation was observed. The presence of phosphatase activity was demonstrated for all the tested fungi. The tested strains of fungi had a positive effect on the general phosphorus content in the dry matter of soybean shoots, this indicator increased notably in the variant with the use of P. funiculosum 20312 — 0.751 % against 0.643 % in the control variant. Conclusions. The tested fungi of the genus Penicillium, isolated from surface-sterilised roots of soybean plants, are capable of releasing phosphorus by dissolving inorganic and mineralising organic phosphates, and have a positive effect on the content of general phosphorus in soybean shoots.
doi_str_mv 10.35868/1997-3004.41.19-33
first_indexed 2025-11-05T02:30:41Z
format Article
fulltext 19 Сільськогосподарська мікробіологія. 2025. Вип. 41. С. 19–33. ISSN 1997-3004 https://doi.org/10.35868/1997-3004.41.19-33 UDC 579.64:582.28:633.34 PHOSPHATE-MOBILISING PROPERTIES OF FUNGI OF THE GENUS PENICILLIUM ISOLATED FROM SOYBEAN HISTOSPHERE O. О. Shakhovnina, https://orcid.org/0000-0001-9105-4116, О. V. Nadkernychna, https://orcid.org/0000-0001-7542-528X, І. M. Pyshchur, https://orcid.org/0009-0000-6719-8427 Institute of Agricultural Microbiology and Agroindustrial Manufacture, NAAS 97 Shevchenka Str., Chernihiv, 14030, Ukraine; e-mail: helenshah@ukr.net Objective. To research the ability of fungi of the genus Penicillium, isolated from the histo- sphere of soybean plants, release phosphorus from mineral and organic phosphates, study their effect on the general phosphorus content in plant shoots. Methods. Microbiological (cultivation of the tested fungi on Pikovska’s medium and its modifications, Czapek-Dox agar with tricalcium phosphate or phenolphthalein phosphate, wort agar), vegetation experiment (content determination of general phosphorus in the aboveground mass of soybean plants), statistical. Results. The use of three insoluble phosphates in Pikovska medium showed that the tested fungi dissolve to varying degrees Са3(РО4)2 and are unable to dissolve AlPO4 and FePO4. On the seventh day of cultivation, clearly visible zones of enlightenment were formed around the colonies of P. funiculosum 20312 and P. variabile 20173, with phosphate dissolution indexes of 1.17 and 1.18, respectively. When cultivating fungi on Pikovska medium with the addition of bromophenol blue dye in P. funiculosum 20312 and P. variabile 20173, the medium quickly changed colour from green to yellow, indicating the diffusion of organic acids produced by the fungi into the agar. Starting from the twelfth day of the experiment, the environment around the colonies of fungi P. glauco-lanosum 20401 also ac- quired a rich yellow colour and the halo zones formation was observed. The presence of phospha- tase activity was demonstrated for all the tested fungi. The tested strains of fungi had a positive ef- fect on the general phosphorus content in the dry matter of soybean shoots, this indicator increased notably in the variant with the use of P. funiculosum 20312 — 0.751 % against 0.643 % in the con- trol variant. Conclusions. The tested fungi of the genus Penicillium, isolated from surface-sterilised roots of soybean plants, are capable of releasing phosphorus by dissolving inorganic and minera- lising organic phosphates, and have a positive effect on the content of general phosphorus in soy- bean shoots. Key words: endophytic fungi of soybean, PSF (phosphate solubilising fungi), inorganic phos- phate dissolution, organic phosphate mineralisation, phosphatase. Introduction. Plants require about 16 mac- ro- and microelements for optimal growth, with phosphorus being the most limiting nutrient for crops productivity after nitrogen [1; 2]. It plays an important role in virtually all major metabo- lic processes in plants, including photosynthesis, respiration, energy metabolism, macromolecular biosynthesis [3] and biological nitrogen fixation in legumes [4]. Adequate phosphorus supply in the early stages of plant development is essen- tial for the establishment of the plants reproduc- tive organs germs. Phosphorus also has a signi- ficant impact on the formation of the root sys- tem and its branching. Phosphorus accounts from 0.05 % to 0.5 % [5], and according to other sources, from 0.2 % to 0.8 % of the plant’s dry matter [6]. This element is found in plants either in the form of a free inorganic orthophos- phate group (Pi) or in the form of organophos- phate compounds [7]. The total amount of Pi © O. О. Shakhovnina, О. V. Nadkernychna, І. M. Pyshchur, 2025 20 in plant cells is divided into two physiologically distinct pools. The first one is located in the cy- toplasm and constitutes the metabolically active Pi pool, and the second one, which is a specific phosphorus reserve, is stored in vacuoles [7]. With a sufficient supply of phosphorus, vacu- oles contain 85–95 % of cellular phosphorus, while the cytoplasmic pool is 5–15 % [8]. Organophosphorus compounds in living or- ganisms are predominantly organic phosphate esters, in which phosphate groups are linked to organic units via a C-O-P bond. The main pools for esterified phosphorus are nucleic acids (DNA and RNA), phosphoproteins, phospholi- pids, sugar phosphates, and energy-rich phos- phate compounds (in particular, adenosine tri- phosphate) [9]. Phospholipids are the class of lipids based on a glycerol backbone to which two long chains of acyl groups of fatty acids and ortho- phosphate acid residues are attached. These sub- stances are not only the most important building blocks of cell membranes, but also participate in membrane transport, cytoskeleton organisation, and signal transduction [10]. Phospholipid me- tabolism plays an important role in seed germi- nation, proper pollen formation, cotyledon vas- cularity, stress reactions, and the transduction of light and sugar signals [11]. Phosphate derivatives of sugars are essen- tial metabolic intermediates and some of them, such as phytic acid (Ins P6), are also a reservoir of phosphorus in plants. In seeds, phytic acid is contained in the form of the mixed salt of potas- sium, magnesium, calcium, manganese, iron and zinc cations and accumulates in membrane- bound inclusions called globules [12]. Depen- ding on the type of plant, the phosphorus con- tent of phytate has been found to be between 30 % and 60 % of the general phosphorus in seeds. In addition to phosphorus storage, the functions of Ins P6 include mRNA export, chromatin remodelling and DNA double-strand break repair. The ability of phytic acid to com- plex with iron ions Fe2+ helps to reduce the for- mation of active oxygen forms during the lipid peroxidation reaction [13]. There are various forms of phosphate deri- vatives of nucleotides containing up to three esterified phosphate residues linked to ribose or deoxyribose links. A large group of phospho- esters nucleoside derivatives (e. g. ATP, ADP, UDP) is a specific primary energy reservoir dis- tributed in phosphorylation and dephosphoryla- tion reactions of other chemical compounds. The role of ATP as an energy source is well known, and extracellular ATP (eATP) in plants is also a specific signalling agent that generates an increase in cytosolic Са2+, promoting plants development and defence reactions [14]. Analysis of recent researches and publi- cations. Although the total amount of phospho- rus in the soil (50–3000 mg/kg) is considered sufficient, the fraction available to plants is less than 1 % of its total amount [15; 16]. Subopti- mal levels of phosphorus nutrition can reduce crop yields by up to 15 % [17]. The effective- ness of chemical phosphate fertilisers is usually less than 30 % due to its fixation either in the form of iron and aluminium phosphates in aci- dic soils [18] or calcium phosphate in neutral and alkaline soils [19]. Phosphorus in soil is found in inorganic and organic forms and is divided into three pools that are in equilibrium with each other. The first pool is called the fixed or unstable fraction and cannot be used by plants. It includes primary minerals (insoluble inorganic phosphates apa- tite, strangite and variscite), sorbed phosphorus (clays, iron and aluminium oxides, carbonates) and organic phosphorus compounds. The se- cond pool contains secondary phosphate mine- rals (calcium, iron and aluminium phosphates) and is known as the active (labile) fraction of phosphorus because it is slowly released for plants absorption. The third pool is the soluble fraction of phosphorus, i. e. inorganic phospho- rus dissolved in water or soil solution and avai- lable to plants (in the form of H2PO4– and HPO42– anions) [20]. The main processes in the soil phosphorus cycle that affect its soluble fraction are: 1) dissolution-precipitation (mineral equilibri- um); 2) sorption-desorption (interaction between phosphorus in soil solution and on the solid sur- face of soil aggregates); 3) mineralisation-im- mobilisation (biologically mediated transfor- mation of phosphorus between inorganic and organic forms) [6; 21]. Microorganisms mobilise insoluble and fixed forms of phosphorus in the soil through dissolution and mineralisation. According to Kucey [22], the number of fungi capable of releasing phosphorus from inso- luble compounds is about 0.1–0.5 % of their to- tal population. Soil fungi capable of converting ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 21 phosphorus into a form accessible to plants have a number of advantages over bacteria: firstly, micromycetes tend to produce more acids than bacteria [23]; secondly, they usually do not lose their ability to dissolve insoluble phosphorus compounds after repeated subcultivation in the laboratory, as it can happen with bacteria; third- ly, fungi in soils can travel long distances more easily, which is important for crops [22]. PSF (phosphate-solubilising fungi) or fungi that dissolve different types of phosphates are representatives of different genera. The best- described PSF in the scientific literature today are micromycetes of the genera Penicillium, As- pergillus, Alternaria, Helminthosporium, Ar- throbotrys, Rhizopus, Fusarium, Trichoderma та Sclerotium [24; 25]. The ability to dissolve mineral phosphates in vitro has been demonstrated for a number of species of the genus Penicillium: P. oxalicum [26–29], P. albidum [30], P. thomii [30], P. res- trictum [30], P. frequentans [30], P. aurantio- griseum [31], P. radicum [32], P. rugulosum [33], P. citrinum [34], P. expansum [35; 36], P. funiculosum [37], P. variabile [38–41], P. italicum [42], P. soli, P. austrosinense [43], P. olsonii [44], P. bilaiae [45], P. guanacasten- se [46]. In addition, there are studies showing the phosphate-mobilising properties of penicilli that have not been identified to species [47–49]. Phosphorus release occurs through the organic acids production (as a result of oxidative respi- ration or fermentation of organic carbon sources), which can either directly dissolve mineral phosphates as a result of anion ex- change or chelate cations Fe3+, Al3+ і Ca2+ [50]. High-performance liquid chromatography me- thod has shown that PSF-penicilli of different species secrete glucuronic [26; 32; 33; 39], oxalic [26; 31], citric [26; 33], malic [26], tarta- ric [23; 26] and lactic [23] acids. The mineralisation of soil organic phos- phates plays an important role in the phosphorus cycle in the agricultural system. Phosphorus in organic compounds can account for 4–90 % of the total soil phosphorus [51]. The mineralisa- tion of organophosphates occurs with the help of the enzymes phosphomonoesterases, phyta- ses, phosphonatases and C-P lyases. Phospho- monoesterases (often simply referred to as phosphatases), which are the most common and best studied [52], dephosphorylate phospho- esters or phosphoanhydride bonds of organic matter. Phytases specifically cause the release of phosphorus through the decomposition of phy- tates. Microorganisms are a key factor in regu- lating phytate mineralisation in the soil, and their presence in the rhizosphere compensates for the inability of plants to obtain phosphorus directly from phytate [53]. C-P lyases split the C-P bond of organophosphates [54]. Despite the large number of researches on the ability of penicilli to mobilise phosphorus from organic and inorganic compounds, only few reports on this activity of soybean endo- phytic fungi are available in the literature. Thus, in the article by Khan et al. [37] there is a men- tion that the soybean endophyte P. funiculosum LHL06 dissolves tricalcium phosphate. The effect of phosphate-mobilising Penicil- lium strains on soybean plants is also insuffi- ciently covered in the literature. Noteworthy is the work of El-Azouni [42], whose objects of study were fungi Aspergillus niger and Penicil- lium italicum. Both micromycetes showed the ability to dissolve insoluble phosphate in agar plates, and in Pikovska liquid medium P. itali- cum released 275 µg P/ml, while A. niger re- leased 490 µg P/ml after seven days of incuba- tion. The author found that the simultaneous use of both fungi in the vegetation experiment sig- nificantly increased the dry matter weight and phosphorus content in soybean plants versus the control indicators. Taking into consideration the above men- tioned, the aim of our work was to research the ability of soybean endophytes of the genus Pe- nicillium to release phosphorus from mineral and organic phosphates, to study their effect on the content of total phosphorus in plant shoots. Materials and methods. Fungal strains involved in the researches (Penicillium funiculosum 20312, P. variabile 20173, P. glauco-lanosum 20401), isolated from surface-sterilised roots of soybean plants of the Legend variety grown on sod-medium podzolic dusty sandy loam soil and identified by morpho- logical and cultural characteristics [56]. The ability of the tested fungal strains to dissolve mineral phosphates was studied by the method of agar plates on Pikovska medium [57] with the addition of Са3(РО4)2, AlPO4, FePO4 in various variants as the only source of phospho- rus. When microorganisms characterised by this ability are cultivated, transparent zones of light are formed around the colonies. Additionally, ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 22 modifications of Pikovska medium [58; 59] and Czapek-Dox agar with the addition of 5 g/l Са3(РО4)2 were used. The sizes of fungal co- lonies and light zones were measured on the seventh day of cultivation. The phosphate solu- bility index (PSI) was calculated as the quotient of the diameter of the zone of enlightenment di- vided by the diameter of the colony [60]. The ability of the tested penicilli to synthe- sise the enzyme phosphatase was determined on Czapek-Dox medium, which did not contain a source of available phosphorus-potassium hy- drophosphate. Instead, sodium phenolphthalein phosphate (10 % solution in ammonia buffer) was sterilely added to the molten medium cooled to 40 °C before inoculation of the fungi in an amount of 1 ml/l. On the fifth day of mi- cromycetes cultivation, Petri dishes with fungal colonies were kept for 10 min in ammonia va- pour (5 drops of 25 % ammonia solution were added to the lids of the Petri dishes). The pres- ence of phosphatase was determined by the ap- pearance of crimson colour under and around the fungal colonies (phenolphthalein, which was formed as a result of dephosphorylation of sodi- um phenolphthalein phosphate with the partici- pation of phosphatase, turns crimson in alkaline medium) [61]. The vegetation experiment was conducted in a vegetation house on soddy-medium podzo- lic dusty sandy loam soil characterised by the following agrochemical parameters: humus con- tent was 1.02 %; nitrogen (according to Korn- field) — 54.9 mg/kg; mobile forms of phospho- rus (according to Kirsanov) — 110–120 mg P2O5; exchangeable potassium (according to Kirsanov) — 120–130 mg K2O per 1 kg of soil; pHsol. — 5,2; pHwater 6.0. Soybean seeds of the Arnica variety were used. Soil moisture was maintained at 60 % of the total moisture capaci- ty. The experiment was repeated five times. The phosphorus content in the aboveground mass was determined on the 35th day. In order to obtain micromycete spores for pre-sowing handling of soybean seeds, the stu- died fungi of the genus Penicillium were grown on wort agar for 10 days. The inoculation load was 1×105 spores per seed. Scheme of the vegetation experiment: 1. Control (wetting the seeds with sterile tap water at the rate of 1.5 % by weight of seeds). 2. Soybean seed handling with fungal spo- res P. funiculosum 20312. 3. Soybean seed handling with fungal spo- res P. variabile 20173. 4. Soybean seed handling with fungal spo- res P. glauco-lanosum 20401. The phosphorus content in the aboveground mass of plants and in soybean grain was deter- mined by the Denige method in the modification of Bouvaitier [61]. Wet ashing of plant material was carried out by the method of V. T. Kurkaiev [61]. The results and their discussion. Taking into consideration that phosphorus is fixed in soils not only in the form of calcium phosphate, but also in the form of iron and aluminium phosphates, which depends on soil acidity, Ba- shan et al. [55] it is recommend to use several sources of insoluble phosphate when studying the phosphate-mobilising properties of microor- ganisms. We evaluated the ability of endophy- tic fungi of the genus Penicillium associated with soybean roots, to dissolve Са3(РО4)2, AlPO4 or FePO4 salts in Pikovska medium (PVK) (Table 1). According to the results obtained, the stu- died strains formed colonies with a diameter of 36.7–42.3 mm on the medium with Са3(РО4)2, 24,7–38,0 mm on the medium with AlPO4 and 26,3–40,0 mm on the medium with FePO4 Table 1. Phosphate dissolution during cultivation of soybean-associated endophytic fungi of the genus Penicillium on Pikovska medium (the 7th day) Variants Insoluble phosphates in the medium Са3(РО4)2 AlPO4 FePO4 colony diameter, mm PSI colony diameter, mm PSI colony diameter, mm PSI P. funiculosum 20312 42,3 ± 0,3 1,17 ± 0,01 38,0 ± 0,6 – 40,0 ± 0,6 – P. variabile 20173 42,7 ± 0,3 1,18 ± 0,01 30,3 ± 0,3 – 30,3 ± 0,3 – P. glauco-lanosum 20401 36,7 ± 0,3 – 24,7 ± 0,3 – 26,3 ± 0,3 – ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 23 (Table 1). However, clearly visible zones of en- lightenment were formed only around the colo- nies of P. funiculosum 20312 and P. variabile 20173 mm on the medium with Са3(РО4)2, the phosphate dissolution indices (PSI) determined on the seventh day of observation were 1.17 and 1.18, respectively (Table 1, Fig. 1 a, b). In order to clarify the ability of P. glauco- lanosum 20401 to produce organic acids, the fungus was additionally cultured on modifica- tions of Pikovska medium and Czapek-Dox agar with Са3(РО4)2 as the only source of phosphate (Table 2). Phosphate-mobilising microorga- nisms differ significantly in the amount and quality of organic acids they produce. Organic acids have different diffusion rates in the agari- fied medium. To eliminate the cases when iso- lates, capable of dissolving mineral phosphates, do not form visible zones of enlightenment on agar plates, Gupta et al. [58] proposed to modify Pikovska agar by adding bromophenol blue dye, which reacts to changes in the pH of the medi- um. When all the studied strains were cultivated on this medium, we observed a change from green (in the control) to yellow of varying in- tensity, which is associated with the diffusion of organic acids produced by fungi into the agar (Fig. 2). On the seventh day of observation, clearly visible zones of enlightenment were formed only around the colonies P. funiculo- sum 20312 and P. variabile 20173 (Fig. 2 b, c), the phosphate dissolution index was 1.13 for both fungi (Table 2). On the twelfth day of cul- tivation, halo zones were also formed around the colonies of P. glauco-lanosum 20401 (Fig. 2 e). The medium proposed by Nautiyal (Nation- al Botanical Research Institute) for phosphate- dissolving microorganisms (NBRIP) [59] was created as a result of studying the effect of the concentrations of individual components of the a b c Fig. 1. Colonies of soybean-associated endophytic fungi of the genus Penicillium on Pikovska medium with Са3(РО4)2 (the 7th day): а) P. funiculosum 20312, b) P. variabile 20173, c) P. gla- uco-lanosum 20401. Table 2. Dissolution of tricalcium phosphate during cultivation of soybean endophytic fungi of the genus Penicillium on modified variants of Pikovska agar and Czapek-Dox medium (the 7th day) Variants Medium with Са3(РО4)2 PVK with bromothymol addition NBRIP Czapek-Dox colony diameter, mm PSI colony diameter, mm PSI colony diameter, mm PSI P. funiculosum 20312 39,3 ± 0,3 1,13 ± 0,02 32,7 ± 0,3 1,12 ± 0,02 34,0 ± 0,6 1,12 ± 0,00 P. variabile 20173 38,7 ± 0,9 1,13 ± 0,01 35,3 ± 0,3 1,08 ± 0,01 44,3 ± 0,3 1,11 ± 0,01 P. glauco-lanosum 20401 30,0 ± 0,6 – 23,7 ± 0,3 – 31,0 ± 0,6 – ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 24 a b c d e Fig. 2. Colonies of soybean-associated endophytic fungi of the genus Penicillium on Pikovska medium with bromophenol blue: а) control (medium without colonies), b) P. funiculo- sum 20312 (the 7th day), c) P. variabile 20173 (the 7th day), d) P. glauco-lanosum 20401 (the 7th day), e) P. glauco-lanosum 20401 (the 12th day). Pikovska medium on the activity of phospha- te dissolution by a number of microorganisms. The author showed a positive effect of the in- creased content of magnesium salts in the medi- um. We chose Czapek-Dox agar because the composition of this medium is optimal for growing fungi, in particular, representatives of the genus Penicillium, which are the objects of this research. The phosphate dissolution in- dexes determined using the modified media and Czapek-Dox agar were slightly inferior to the corresponding results obtained on Pikovska me- dium (Table 2). In the studies on the selection of phosphate- mobilising fungi, the selected strains are usually characterised by phosphate dissolution indexes that are significantly higher than those obtained by us when cultivating the studied fungi in dif- ferent mediums [47; 49; 62]. In our opinion, this is due to the adaptation of endophytic peni- cilli associated with soybean plants to the topo- logical zone from which they were isolated, since excessive acid formation would disrupt the biochemical balance of the internal tissues of roots. Thus, all the tested fungi are capable of producing organic acids and releasing phospho- rus from Са3(РО4)2 to varying degrees. This ability is described in the literature for repre- sentatives of the species P. funiculosum and P. variabile [37; 40]. Since another important mechanism of phosphorus conversion into a form accessible to plants is the mineralisation of organic phos- phates, the presence of the phosphatase enzyme in the tested penicillium strains was checked. This enzymatic activity was observed for all three fungi. The fungal phosphatases depho- sphorylate sodium phenolphthalein phosphate added to the Czapek-Dox medium, and the re- leased phenolphthalein is coloured bright crim- son in ammonia vapour (Fig. 3). According to Bashan et al. [55], a necessary step in the research of phosphate mobilising properties of a microorganism is to determine the direct contribution of phosphorus to inocu- lated plants. Taking this into consideration, we determined the content of general phosphorus (Р2О5) in the aboveground mass of plants grown under the conditions of the vegetation experi- ment (Fig. 4). According to the data obtained, all the tested fungal strains had a positive effect on the content of general phosphorus in the dry matter of soybean shoots, but this indicator in- creased significantly in the variant with the use of P. funiculosum 20312 and was (0.751 ± ± 0.046) % against (0.643 ± 0.008) % in the control variant (Fig. 4). Literature data shows that the ability of mi- croorganisms to mobilise phosphorus does not necessarily correlate with the ability to stimulate plant growth [63]. However, our previous re- searches have shown a multidirectional effect of penicilliums on soybean plants. The tested strains produce phytohormonal substances, which in turn have a positive effect on both growth performance and the symbiotic appa- ratus of soybean plants [56]. ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 25 a b c Fig. 3. Qualitative response to phosphatase during cultivation of Penicillium fungi on Czapek- Dox medium with sodium phenolphthalein phosphate (the 5th day): а) P. funiculosum 20312; b) P. variabile 20173; c) P. glauco-lanosum 20401; the top row of photos — fungal colonies before processing with ammonia vapour; the bottom row — fungal colonies after exposure to ammonia vapour. Fig. 4. Influence of endophytic fungi of the genus Penicillium on the content of general phos- phorus in shoots of soybean plants of the Arnica variety (vegetation experiment, budding — beginning of blooming): 1 — control (water); 2 — P. funiculosum 20312; 3 — P. variabi- le 20173; 4 — P. glauco-lanosum 20401. Conclusions. The tested fungi of the genus Penicillium, isolated from surface-sterilised roots of soybean plants, are capable of releasing phosphorus by dissolving inorganic and mine- ralising organic phosphates. There is a tendency to increase the content of general phosphorus in the aboveground mass of soybean plants after processing soybean seeds with P. variabi- le 20173 and P. glauco-lanosum 20401 spores and a significant increase from 0.643 % in the control to 0.751 % in the variant with the use of the fungus P. funiculosum 20312. REFERENCES 1. Zornoza, R., Acosta, J. A., Bastida, F., Do- mínguez, S. G., Toledo, D. M., & Faz, A. (2015). Identification of sensitive indicators to assess the in- terrelationship between soil quality, management practices and human health. Soil, 1, 173–185. https://doi.org/10.5194/soil-1-173-2015 2. Gotz, L. F., Holzschuh, M. J., Vargas, V. P., Teles, A. P. B., Martins, M. M., & Pavinato, P. S. (2023). Phosphate management for high soybean and maize yields in expansion areas of Brazilian Cerrado. Agronomy, 13, 158. http://dx.doi.org/10. 3390/agronomy13010158 0,0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9 1 2 3 4 G en er al p ho sp ho ru s c on te nt ,% ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 26 3. Khan, M. S., Zaidi, A., Ahemad, M., Oves, M., & Wani, P. A. (2010). Plant growth pro- motion by phosphate solubilizing fungi — current perspective. Arch Agron Soil Sci, 56, 73–98. https://doi.org/10.1080/03650340902806469 4. Saber, K., Nahla, L. D., & Chedly, A. (2005). Effect of P on nodule formation and N fixation in bean. Agron Sustain Dev, 25, 389–393. https://doi. org/10.1051/agro:2005034 5. Johri, A. K., Oelmuller, R., Dua, M., Ya- dav, V., Kumar, M., Tuteja, N. … Stroud, R. M. (2015). Fungal association and utilization of phos- phate by plants: success, limitations, and future pro- spects. Front Microbiol, 6, 984. https://doi.org/ 10.3389/fmicb.2015.00984 6. Sharma, S. B., Sayyed, R. Z., Trivedi, M. H., & Gobi, T. A. (2013). Phosphate solubilizing mi- crobes: sustainable approach for managing phospho- rus deficiency in agricultural soils. SpringerPlus, 2, 587. https://doi.org/10.1186/2193-1801-2-587 7. Veneklaas, E. J., Lambers, H., Bragg, J., Fin- negan, P. M., Lovelock, C. E., Plaxton, W. C. … Raven, J. A. (2012). Opportunities for improving phosphorus-use efficiency in crop plants. New Phy- tol, 195, 306–320. https://doi.org/10.1111/j.1469- 8137.2012.04190.x 8. Akhtar, M. S., Oki, Y., & Adachi, T. (2008). Intraspecific variations of phosphorus absorption and remobilization, P forms, and their internal buf- fering in Brassica cultivars exposed to a P-stressed environment. J Integr Plant Biol, 50, 703–716. https://doi.org/10.1111/j.1744-7909.2008.00675.x 9. Dissanayaka, D., Ghahremani, M., Siebers, M., Wasaki, J., & Plaxton, W. C. (2021). Recent insights into the metabolic adaptations of phosphorus- deprived plants. J Exp Bot, 72(2), 199–223. https:// doi.org/10.1093/jxb/eraa482 10. Kasamo, K, Nouchi, I. (1987). The role of phospholipids in plasma membrane ATPase activity in Vigna radiata L. (mung bean) roots and hypoco- tyls. Plant Physiol, 83, 323–328. https://doi.org/ 10.1104/pp.83.2.323 11. Xue, H. W., Chen, X., & Mei, Y. (2009). Function and regulation of phospholipid signalling in plants. Biochem J, 421, 145–156. https://doi.org/ 10.1042/bj20090300 12. White, P. J., Veneklaas, E. J. (2012). Nature and nurture: the importance of seed phosphorus con- tent. Plant Soil, 357, 1–8. https://doi.org/10.1007/ s11104-012-1128-4 13. Doria, E., Galleschi, L., Calucci, L., Pinzi- no, C., Pilu, R., Cassani, E., & Nielsen, E. (2009). Phytic acid prevents oxidative stress in seeds: evi- dence from a maize (Zea mays L.) low phytic acid mutant. J Exp Bot, 60(3), 967–978. https://doi.org/ 10.1093/jxb/ern345 14. Roux, S. J., Steinebrunner, I. (2007). Extra- cellular ATP: an unexpected role as a signaler in plants. Trends Plant Sci, 12(11), 522–527. https:// doi.org/10.1016/j.tplants.2007.09.003 15. Yadav, R. S., Meena, S. C., Patel, S. I., Pa- tel, K. I., Akhtar, M. S., Yadav, B. K., & Panwar, J. (2012). Bioavailability of soil P for plant nutrition. In E. Lichtfouse (Ed.). Farming for Food and Water Security. (pp. 177–200). Dordrecht: Springer. https:// doi.org/10.1007/978-94-007-4500-1_8 16. Weihrauch, C., Opp, C. (2018). Ecological- ly relevant phosphorus pools in soils and their dy- namics: The story so far. Geoderma, 325, 183–194. https://doi.org/10.1016/j.geoderma.2018.02.047 17. Li, C. K., Li, Q. S., Wang, Z. P., Ji, G. N., Zhao, H., Gao, F. … Li, H. X. (2019). Environmen- tal fungi and bacteria facilitate lecithin decomposi- tion and the transformation of phosphorus to apatite. Sci Rep, 9, 15291. https://doi.org/10.1038/s41598- 019-51804-7 18. Norrish, K., Rosser, H. (1983). Mineral phos- phate. In Soils: an Australian viewpoint. (pp. 335– 361). Melbourne, CSIRO/London, UK, Australia: Academic Press. 19. Lindsay, W. L., Vlek, P. L. G., & Chi- en, S. H. (1989). Phosphate minerals. In J. B. Dixon, S. B. Weed (Eds.). Minerals in soil environment. (pp. 1089–1130). Madison: WI. 20. Gómez-Gallego, T., Sánchez-Castro, I., Mo- lina, L., Trasar-Cepeda, C., García-Izquierdo, C., Ramos, J. L., & Segura, A. (2025). Phosphorus ac- quisition by plants: Challenges and promising stra- tegies for sustainable agriculture in the 21st century. Pedosphere, 35(1), 193–215. https://doi.org/10.1016/ j.pedsph.2024.05.002 21. Bünemann, E. K. (2015). Assessment of gross and net mineralization rates of soil organic phosphorus — A review. Soil Biol Biochem, 89, 82– 98. https://doi.org/10.1016/j.soilbio.2015.06.026 22. Kucey, R. M. N. (1983). Phosphate solubi- lizing bacteria and fungi in various cultivated and virgin Alberta soils. Can J Soil Sci, 63, 671–678. https://doi.org/10.4141/cjss83-068 23. Venkateswarlu, B., Rao, A. V., Raina, P., & Ahmad, N. (1984). Evaluation of phosphorus solu- bilization by microorganisms isolated from arid soil. J Indian Soc Soil Sci, 32(2), 273–277. 24. da Silva, L. I., Pereira, M. C., de Carva- lho, A. M. X., Buttrós, V. H., Pasqual, M., & Dó- ria, J. (2023). Phosphorus-solubilizing microorga- nisms: A key to sustainable agriculture. Agricul- ture, 13(2), 462. https://doi.org/10.3390/agriculture 13020462 25. Fu, S.-F., Balasubramanian, V. K., Chen, C.-L., Tran, T. T., Muthuramalingam, J. B., & Chou, J.-Y. (2024). The phosphate-solubilising fungi in ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 27 sustainable agriculture: unleashing the potential of fungal biofertilisers for plant growth. Folia Micro- biol, 69, 697–712. https://doi.org/10.1007/s12223- 024-01181-0 26. Xiao, C., Chi, R., & Hu, L. (2013). Solubi- lization of aluminum phosphate by specific Penicil- lium spp. J Cent South Univ, 20, 2109–2114. https:// doi.org/10.1007/s11771-013-1714-5 27. Li, Z., Bai, T., Dai, L., Wang, F., Tao, J., Meng, S. … Hu, S. (2016). A study of organic acid production in contrasts between two phosphate solu- bilizing fungi: Penicillium oxalicum and Aspergillus niger. Sci Rep, 6, 25313. https://doi.org/10.1038/ srep25313 28. Jiang, Y., Ge, F., Li, F., Zhang, D., Seng, D., & Jian, T. (2020). Intracellular Metabolomics Swit- ching Alters Extracellular Acid Production and In- soluble Phosphate Solubilization Behavior in Peni- cillium oxalicum. Metabolites, 10(11), 441. https:// doi.org/10.3390/metabo10110441 29. Tong, J., Wu, H., Jiang, X., Ruan, C., Li, W., Zhang, H. … Shi, J. (2024). Dual Regulatory Role of Penicillium oxalicum SL2 in Soil: Phosphorus Solubilization and Pb Stabilization. Environ Sci Technol, 58(1), 603–616. https://doi.org/10.1021/ acs.est.3c08881 30. Morales, M., Alvear, E., Valenzuela, C. E., & Castillo, F. B. (2011). Screening, evaluation and selection of phosphate-solubilising fungi as potential biofertilise. Journal of Soil Science and Plant Nut- rition, 11(4), 89–103. http://dx.doi.org/10.4067/ S0718-95162011000400007 31. Hu, J., Wang, L., Zhang, L., Gao, H., & Tian, D. (2022). A Study of Phosphate Solubilizing Capacity by Penicillium Aurantiogriseum under Dif- ferent Carbon and Nitrogen Resources. E3S Web of Conferences, 350, 03002. http://dx.doi.org/10.1051/ e3sconf/202235003002 32. Whitelaw, M. A., Harden, T. J., & Hel- yar, K. R. (1999). Phosphate solubilisation in solu- tion culture by the soil fungus Penicillium radicum. Soil Biol Biochem, 31(5), 655–665. https://doi.org/ 10.1016/S0038-0717(98)00130-8 33. Reyes, I., Baziramakenga, R., Bernier, L., & Antoun, H. (2001). Solubilization of phosphate rocks and minerals by a wild-type strain and two UV-induced mutants of Penicillium rugulosum. Soil Biol Biochem, 33(12–13), 1741–1747. https://doi. org/10.1016/S0038-0717(01)00099-2 34. Mittal, V., Singh, O., Nayyar, H., Kaur, J., & Tewari, R. (2008). Stimulatory effect of phos- phate-solubilizing fungal strains (Aspergillus awa- mori and Penicillium citrinum) on the yield of chickpea (Cicer arietinum L. cv. GPF2). Soil Biol Biochem, 40(3), 718–727. https://doi.org/10.1016/ j.soilbio.2007.10.008 35. Morales, H., Marín, S., Ramos, A. J., & Sanchis, V. (2010). Influence of post-harvest tech- nologies applied during cold storage of apples in Penicillium expansum growth and patulin accumu- lation: a review. Food Control, 21(7), 953–962. https://doi.org/10.1016/j.foodcont.2009.12.016 36. Panchal, B. J., Patel, S., Rajkumar, S. J., Mahatma, L., & Singh, D. (2016). Isolation and identification of phosphate solubilizing Penicillium expansum NAUG-B1 and their consequence on growth of brinjal. Ecol Environ Conserv, 21, 259– 267. 37. Khan, A. L., Hamayun, M., Kim, Y.-H., Kang, S.-M., & Lee, I.-J. (2011). Ameliorative sym- biosis of endophyte (Penicillium funiculosum LHL06) under salt stress elevated plant growth of Glycine max L. Plant Physiol Biochem, 49(8), 852– 861. https://doi.org/10.1016/j.plaphy.2011.03.005 38. Yasser, M. M., Ahmed, A. S. M., Osa- ma, N. M., & Nasr, S. H. (2014). Solubilization of inorganic phosphate by phosphate solubilizing fungi isolated from Egyptian soils. J Biol Earth Sci, 4(1), 83–90. 39. Fenice, M., Selbman, L., Federici, F., & Vassilev, N. (2000). Application of encapsulated Penicillium variabile P16 in solubilization of rock phosphate. Bioresource Technology, 73(2), 157–162. https://doi.org/10.1016/S0960-8524(99)00150-9 40. Crognale, S., Petruccioli, M., Fenice, M., & Federici, F. (2008). Fed-batch gluconic acid produc- tion from Penicillium variabile P16 under different feeding strategies. Enzyme and Microbial Technolo- gy, 42(5), 445–449. https://doi.org/10.1016/j.enzmic tec.2008.01.002 41. Kanse, O. S., Whitelaw-Weckert, M., Ka- dam, T. A., & Bhosale, H. J. (2015). Phosphate so- lubilization by stress-tolerant soil fungus Talaromy- ces funiculosus SLS8 isolated from the Neem rhizo- sphere. Ann Microbiol, 65, 85–93. https://doi.org/ 10.1007/s13213-014-0839-6 42. El-Azouni, I. M. (2008). Effect of phos- phate solubilizing fungi on growth and nutrient up- take of soyabean (Glycine max L.) plants. Journal of Applied Science Research, 4, 592–598. 43. Doilom, M., Guo, J.-W., Phookamsak, R., Mortimer, P. E., Karunarathna, S. C., Dong, W. … Xu, J.-C. (2020). Screening of Phosphate-Solubili- zing Fungi From Air and Soil in Yunnan, China: Four Novel Species in Aspergillus, Gongronella, Penicillium, and Talaromyces. Front Microbiol, 11. https://doi.org/10.3389/fmicb.2020.585215 44. Suraby, E. J., Agisha, V. N., Dhandapa- ni, S., Sng, Y. H., Lim, S. H., Naqvi, N. I. … Park, B. S. (2023). Plant growth promotion under phosphate deficiency and improved phosphate ac- quisition by new fungal strain, Penicillium olsonii ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 28 TLL1. Front Microbiol, 14. https://doi.org/10.3389/ fmicb.2023.1285574 45. Takeda, M., Knight, J. D. (2006). Enhanced solubilization of rock phosphate by Penicillium bilaiae in pH-buffered solution culture. Can J Mi- crobiol, 51(11), 1121–1129. https://doi.org/10.1139/ w06-074 46. Qiao, H., Sun, X.-R., Wu, X.-Q., Li, G.-E., Wang, Z., & Li, D.-W. (2019). The phosphate- solubilizing ability of Penicillium guanacastense and its effects on the growth of Pinus massoniana in phosphate-limiting conditions. Biol Open, 8(11). https://doi.org/10.1242/bio.046797 47. Henri, F., Laurette, N. N., Ghislain, N. N., Vanessa, T. T. G., Virginie, T. I. A., & Dieudon- né, N. (2014). Rock phosphate solubilisation by strains of Penicillium spp. isolated from farm and forest soils of three agro ecological zones of Ca- meroon. American Journal of Agriculture and Forestry, 2(2), 25–32. https://doi.org/10.11648/ j.ajaf.20140202.12 48. Mahadevamurthy, M., Channappa, T. M, Sidappa, M., Raghupathi, M. S, & Nagaraj, A. K. (2016). Isolation of phosphate solubilizing fungi from rhizosphere soil and its effect on seed growth parameters of different crop plants. Journal of Applied Biology & Biotechnology, 4(6), 22–26. http://dx.doi.org/10.7324/JABB.2016.40604 49. Elias, F., Woyessa, D., & Muleta, D. (2016). Phosphate solubilization potential of rhizo- sphere fungi isolated from plants in Jimma Zone, Southwest Ethiopia. Int J Microbiol, 1–11. http:// dx.doi.org/10.1155/2016/5472601 50. Omar, S. A. (1998). The role of rock phos- phate solubilizing fungi and vesicular arbuscular mycorrhiza (VAM) in growth of wheat plants fer- tilized with rock phosphate. World J Microbiol Bio- technol, 14, 211–219. http://dx.doi.org/10.1023/ A:1008830129262 51. Khan, M. S., Zaidi, A., & Wani, P. A. (2009). Role of phosphate solubilising microorga- nisms in sustainable agriculture. In E. Lictfouse, M. Navarrete, P. Debaeke, S. Véronique, C. Albe- rola (Eds.). Sustainable Agriculture. (pp. 551–570). Dordrecht: Springer. https://doi.org/10.1007/978-90- 481-2666-8_34 52. Nannipieri, P., Giagnoni, L., Landi, L., & Renella, G. (2011). Role of phosphatase enzymes in soil. In E. Bunemann, A. Oberson, E. Frossard (Eds.). Phosphorus in Action. Soil Biology, 26 (pp. 251–244). Heidelberg: Springer. https://doi.org/ 10.1007/978-3-642-15271-9_9 53. Richardson, A. E., Simpson, R. J. (2011). Soil microorganisms mediating phosphorus availa- bility. Plant Physiol, 156, 989–996. https://doi.org/ 10.1104/pp.111.175448 54. Rodriguez, H., Fraga, R., Gonzalez, T., & Bashan, Y. (2006). Genetics of phosphate solubiliza- tion and its potential applications for improving plant growth-promoting bacteria. Plant Soil, 287, 15–21. https://doi.org/10.1007/s11104-006-9056-9 55. Bashan, Y., Kamnev, A. A., & de Bashan, L. E. (2013). Tricalcium phosphate is inappropriate as a universal selection factor for isolating and tes- ting phosphate-solubilizing bacteria that enhance plant growth: a proposal for an alternative proce- dure. Biol Fertil Soils, 49, 465–479. https://doi.org/ 10.1007/s00374-012-0737-7 56. Shakhovnina О. О., Nadkernychna О. V., & Horbatok А.V. (2023). Vplyv hrybiv rodu Penicilli- um, izolovanykh z koreniv soi, na symbiotychnu systemu «Glycine max – Bradyrhizobium japoni- cum» ta produktyvnist kultury [The influence of Penicillium fungi isolated from soybean roots on the symbiotic system “Glycine max – Bradyrhizobium japonicum” and crop productivity]. Silskohospo- darska Mikrobiolohiia — Agricultural Microbio- logy, 38, 16–28 [in Ukrainian]. https://doi.org/10. 35868/1997-3004.38 57. Pikovskaya R. I. (1948). Mobilization of phosphorus in soil in connection with vital activity of some microbial species. Microbiology, 17, 362– 370. 58. Gupta, R., Singal, R., Shankar, A., Ku- had, R. C., Saxena, R. K. (1994). A modified plate assay for screening phosphate solubilizing microor- ganisms. J Gen Appl Microbiol, 40, 255–260. https://doi.org/10.2323/JGAM.40.255 59. Nautiyal, C. S. (1998). An efficient micro- biological growth medium for screening phosphate solubilizing microorganisms. FEMS Microbiology Letters, 170, 265–270. https://doi.org/10.1016/S0378- 1097(98)00555-2 60. Premono, M. E., Moawad, A. M., & Vlek, P. L. G. (1996). Effect of phosphate-solubi- lizing Pseudomonas putida on the growth of maize and its survival in the rhizosphere. Indonesian Jour- nal of Crop Science, 11, 13–23. 61. Volkohon, V. V., Nadkernychna, O. V., Tokmakova, L. M., Melnychuk, T. M., & Chai- kovska, L. O. (2010). Eksperymentalna gruntova mikrobiolohiia [Experimental soil microbiology]. Kyiv: Ahrarna nauka — Agrarian science [in Ukrai- nian]. 62. Nasr, S. H., Mousa, A. S. M., Yasser, M. M., & Marzouk, M. A. (2021). Antagonistic potential of some phosphate solubilizing fungi against some phyto-pathogenic fungi. Beni-Suef University Jour- nal of Basic and Applied Sciences, 10, 70. https:// doi.org/10.1186/s43088-021-00159-y 63. Collavino, M. M., Sansberro, P. A., Mro- ginski, L. A., & Aguilar, O. M. (2010). Comparison ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 29 of in vitro solubilization activity of diverse phos- phate-solubilizing bacteria native to acid soil and their ability to promote Phaseolus vulgaris growth. Biol Fertil Soils, 46, 727–738. https://doi.org/10. 1007/s00374-010-0480-x Received: 21.02.2025 Accepted: 25.04.2025 Published online: 17.09.2025 https://doi.org/10.35868/1997-3004.41.19-33 УДК 579.64:582.28:633.34 ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ О. О. Шаховніна, https://orcid.org/0000-0001-9105-4116, О. В. Надкернична, https://orcid.org/0000-0001-7542-528X, І. М. Пищур, https://orcid.org/0009-0000-6719-8427 Інститут сільськогосподарської мікробіології та агропромислового виробництва НААН вул. Шевченка, 97; м. Чернігів, 14030, Україна; e-mail: helenshah@ukr.net Мета. Дослідити здатність грибів роду Penicillium, ізольованих із гістосфери рослин сої, вивільняти фосфор із мінеральних та органічних фосфатів, вивчити їхній вплив на вміст загального фосфору в пагонах рослин. Методи. Мікробіологічні (культивування досліджува- них грибів на середовищі Піковської та його модифікаціях, агарі Чапека-Докса із додаванням трикальційфосфату або фенолфталеїнфосфату, сусловому агарі), вегетаційного досліду (визначення вмісту загального фосфору в надземній масі рослин сої), статистичні. Резуль- тати. Використання трьох нерозчинних фосфатів у складі середовища Піковської показа- ло, що досліджувані гриби різною мірою розчиняють Са3(РО4)2 і не здатні розчиняти AlPO4 та FePO4. На сьому добу культивування навколо колоній P. funiculosum 20312 і P. variabile 20173 утворювалися добре помітні зони просвітлення, індекси розчинення фосфату стано- вили 1,17 і 1,18 відповідно. За культивування грибів на середовищі Піковської з додаванням бромфенолового синього барвника у варіантах P. funiculosum 20312 і P. variabile 20173 сере- довище швидко змінювало колір з зеленого на жовтий, що свідчить про дифузію в агар орга- нічних кислот, продукованих грибами. Починаючи з дванадцятої доби досліду, середовище навколо колоній гриба P. glauco-lanosum 20401 також набувало насиченого жовтого кольо- ру і було відзначено появу гало-зон. Для всіх досліджуваних грибів показано наявність фос- фатазної активності. Досліджувані штами грибів позитивно впливали на вміст загального фосфору в сухій речовині пагонів сої, достовірно цей показник підвищувався у варіанті із застосуванням P. funiculosum 20312 — 0,751 % проти 0,643 % у контрольному варіанті. Висновки. Досліджувані гриби роду Penicillium, ізольовані з поверхнево стерилізованих ко- ренів рослин сої, здатні вивільняти фосфор за рахунок розчинення неорганічних і мінералі- зації органічних фосфатів, позитивно впливають на вміст загального фосфору в пагонах рослин сої. Ключові слова: гриби-ендофіти сої, PSF (гриби, які розчиняють фосфати), розчинення неорганічних фосфатів, мінералізація органічних фосфатів, фосфатаза. ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 30 ЦИТОВАНА ЛІТЕРАТУРА 1. Zornoza R., Acosta J. A., Bastida F., Domín- guez S. G., Toledo D. M., Faz A. Identification of sensitive indicators to assess the interrelationship between soil quality, management practices and human health. Soil. 2015. № 1. P. 173–185. https://doi.org/10.5194/soil-1-173-2015 2. Gotz L. F., Holzschuh M. J., Vargas V. P., Teles A. P. B., Martins M. M., Pavinato P. S. Phos- phate management for high soybean and maize yields in expansion areas of Brazilian Cerrado. Agronomy. 2023. № 13. 158. http://dx.doi.org/10. 3390/agronomy13010158 3. Khan M. S., Zaidi A., Ahemad M., Oves M., Wani P. A. Plant growth promotion by phosphate solubilizing fungi — current perspective. Arch Agron Soil Sci. 2010. № 56. P. 73–98. https://doi. org/10.1080/03650340902806469 4. Saber K., Nahla L. D., Chedly A. Effect of P on nodule formation and N fixation in bean. Agron Sustain Dev. 2005. № 25. P. 389–393. https://doi. org/10.1051/agro:2005034 5. Johri A. K., Oelmuller R., Dua M., Yadav V., Kumar M., Tuteja N. … Stroud R. M. Fungal asso- ciation and utilization of phosphate by plants: suc- cess, limitations, and future prospects. Front Micro- biol. 2015. № 6. 984. https://doi.org/10.3389/fmicb. 2015.00984 6. Sharma S. B., Sayyed R. Z., Trivedi M. H., Gobi T. A. Phosphate solubilizing microbes: sus- tainable approach for managing phosphorus defi- ciency in agricultural soils. SpringerPlus. 2013. № 2. 587. https://doi.org/10.1186/2193-1801-2-587 7. Veneklaas E. J., Lambers H., Bragg J., Fin- negan P. M., Lovelock C. E., Plaxton W. C. … Ra- ven J. A. Opportunities for improving phospho- rus-use efficiency in crop plants. New Phytol. 2012. № 195. P. 306–320. https://doi.org/10.1111/j.1469- 8137.2012.04190.x 8. Akhtar M. S., Oki Y., Adachi T. Intraspecific variations of phosphorus absorption and remobiliza- tion, P forms, and their internal buffering in Brassica cultivars exposed to a P-stressed environment. J In- tegr Plant Biol. 2008. № 50. P. 703–716. https:// doi.org/10.1111/j.1744-7909.2008.00675.x 9. Dissanayaka D., Ghahremani M., Siebers M., Wasaki J., Plaxton W. C. Recent insights into the metabolic adaptations of phosphorus-deprived plants. J Exp Bot. 2021. Vol. 72, № 2. P. 199–223. https://doi.org/10.1093/jxb/eraa482 10. Kasamo K, Nouchi I. The role of phospho- lipids in plasma membrane ATPase activity in Vigna radiata L. (mung bean) roots and hypocotyls. Plant Physiol. 1987. № 83. P. 323–328. https://doi.org/ 10.1104/pp.83.2.323 11. Xue H. W., Chen X., Mei Y. Function and regulation of phospholipid signalling in plants. Bio- chem J. 2009. № 421. P. 145–156. https://doi.org/ 10.1042/bj20090300 12. White P. J., Veneklaas E. J. Nature and nur- ture: the importance of seed phosphorus content. Plant Soil. 2012. Vol. 357. P. 1–8. https://doi.org/ 10.1007/s11104-012-1128-4 13. Doria E., Galleschi L., Calucci L., Pinzi- no C., Pilu R., Cassani E., Nielsen E. Phytic acid prevents oxidative stress in seeds: evidence from a maize (Zea mays L.) low phytic acid mutant. J Exp Bot. 2009. Vol. 60, № 3. P. 967–978. https://doi.org/ 10.1093/jxb/ern345 14. Roux S. J., Steinebrunner I. Extracellular ATP: an unexpected role as a signaler in plants. Trends Plant Sci. 2007. Vol. 12, Is. 11. P. 522–527. https://doi.org/10.1016/j.tplants.2007.09.003 15. Yadav R. S., Meena S. C., Patel S. I., Pa- tel K. I., Akhtar M. S., Yadav B. K., Panwar J. Bio- availability of soil P for plant nutrition. E. Licht- fouse (Ed.). Farming for Food and Water Security. Dordrecht: Springer, 2012. P. 177–200. https://doi. org/10.1007/978-94-007-4500-1_8 16. Weihrauch C., Opp C. Ecologically relevant phosphorus pools in soils and their dynamics: The story so far. Geoderma. 2018. Vol. 325. P. 183–194. https://doi.org/10.1016/j.geoderma.2018.02.047 17. Li C. K., Li Q. S., Wang Z. P., Ji G. N., Zhao H., Gao F. … Li H. X. Environmental fungi and bacteria facilitate lecithin decomposition and the transformation of phosphorus to apatite. Sci Rep. 2019. № 9. 15291. https://doi.org/10.1038/s41598- 019-51804-7 18. Norrish K., Rosser H. Mineral phosphate. Soils: an Australian viewpoint. Melbourne, CSIRO/ London, UK, Australia : Academic Press, 1983. P. 335–361. 19. Lindsay W. L., Vlek P. L. G., Chien S. H. Phosphate minerals. J. B. Dixon, S. B. Weed (Eds.). Minerals in soil environment. 2nd edition. Madison : WI, 1989. P. 1089–1130. 20. Gómez-Gallego T., Sánchez-Castro I., Mo- lina L., Trasar-Cepeda C., García-Izquierdo C., Ra- mos J. L., Segura A. Phosphorus acquisition by plants: Challenges and promising strategies for sus- tainable agriculture in the 21st century. Pedosphere. 2025. Vol. 35, Is. 1. P. 193–215. https://doi.org/10. 1016/j.pedsph.2024.05.002 21. Bünemann E. K. Assessment of gross and net mineralization rates of soil organic phospho- rus — A review. Soil Biol Biochem. 2015. Vol. 89. P. 82–98. https://doi.org/10.1016/j.soilbio.2015.06. 026 22. Kucey R. M. N. Phosphate solubilizing bac- teria and fungi in various cultivated and virgin ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 31 Alberta soils. Can J Soil Sci. 1983. № 63. P. 671– 678. https://doi.org/10.4141/cjss83-068 23. Venkateswarlu B., Rao A. V., Raina P., Ah- mad N. Evaluation of phosphorus solubilization by microorganisms isolated from arid soil. J Indian Soc Soil Sci. 1984. Vol. 32, Is. 2. P. 273–277. 24. da Silva L. I., Pereira M. C., de Carval- ho A. M. X., Buttrós V. H., Pasqual M., Dória J. Phosphorus-solubilizing microorganisms: A key to sustainable agriculture. Agriculture. 2023. Vol. 13, № 2. 462. https://doi.org/10.3390/agriculture1302 0462 25. Fu S.-F., Balasubramanian V. K., Chen C.-L., Tran T. T., Muthuramalingam J. B., Chou J.-Y. The phosphate-solubilising fungi in sustainable agricul- ture: unleashing the potential of fungal biofertili- sers for plant growth. Folia Microbiol. 2024. № 69. P. 697–712. https://doi.org/10.1007/s12223-024- 01181-0 26. Xiao C., Chi R., Hu L. Solubilization of aluminum phosphate by specific Penicillium spp. J Cent South Univ. 2013. № 20. P. 2109–2114. https://doi.org/10.1007/s11771-013-1714-5 27. Li Z., Bai T., Dai L., Wang F., Tao J., Meng S. … Hu S. A study of organic acid produc- tion in contrasts between two phosphate solubilizing fungi: Penicillium oxalicum and Aspergillus niger. Sci Rep. 2016. № 6. 25313. https://doi.org/10.1038/ srep25313 28. Jiang Y., Ge F., Li F., Zhang D., Seng D., Jian T. Intracellular Metabolomics Switching Alters Extracellular Acid Production and Insoluble Phos- phate Solubilization Behavior in Penicillium oxali- cum. Metabolites. 2020. Vol. 10, № 11. 441. https:// doi.org/10.3390/metabo10110441 29. Tong J., Wu H., Jiang X., Ruan C., Li W., Zhang H. … Shi J. Dual Regulatory Role of Penicil- lium oxalicum SL2 in Soil: Phosphorus Solubiliza- tion and Pb Stabilization. Environ Sci Technol. 2024. Vol. 58, № 1. P. 603–616. https://doi.org/ 10.1021/acs.est.3c08881 30. Morales M., Alvear E., Valenzuela C. E., Castillo F. B. Screening, evaluation and selection of phosphate-solubilising fungi as potential biofertilise. Journal of Soil Science and Plant Nutrition. 2011. Vol. 11, № 4. P. 89–103. http://dx.doi.org/10.4067/ S0718-95162011000400007 31. Hu J., Wang L., Zhang L., Gao H., Tian D. A Study of Phosphate Solubilizing Capacity by Pe- nicillium Aurantiogriseum under Different Carbon and Nitrogen Resources. E3S Web of Conferences. 2022. № 350. 03002. http://dx.doi.org/10.1051/e3 sconf/202235003002 32. Whitelaw M. A., Harden T. J., Helyar K. R. Phosphate solubilisation in solution culture by the soil fungus Penicillium radicum. Soil Biol Biochem. 1999. Vol. 31, Is. 5. P. 655–665. https://doi.org/ 10.1016/S0038-0717(98)00130-8 33. Reyes I., Baziramakenga R., Bernier L., Antoun H. Solubilization of phosphate rocks and minerals by a wild-type strain and two UV-indu- ced mutants of Penicillium rugulosum. Soil Biol Biochem. 2001. Vol. 33, Is. 12–13. P. 1741–1747. https://doi.org/10.1016/S0038-0717(01)00099-2 34. Mittal V., Singh O., Nayyar H., Kaur J., Tewari R. Stimulatory effect of phosphate-solu- bilizing fungal strains (Aspergillus awamori and Penicillium citrinum) on the yield of chickpea (Cicer arietinum L. cv. GPF2). Soil Biol Biochem. 2008. Vol. 40, Is. 3. P. 718–727. https://doi.org/10.1016/ j.soilbio.2007.10.008 35. Morales H., Marín S., Ramos A. J., San- chis V. Influence of post-harvest technologies applied during cold storage of apples in Penicil- lium expansum growth and patulin accumulation: a review. Food Control. 2010. Vol. 21, № 7. P. 953–962. https://doi.org/10.1016/j.foodcont.2009. 12.016 36. Panchal B. J., Patel S., Rajkumar S. J., Ma- hatma L., Singh D. Isolation and identification of phosphate solubilizing Penicillium expansum NAUG-B1 and their consequence on growth of brin- jal. Ecol Environ Conserv. 2016. № 21. P. 259–267. 37. Khan A. L., Hamayun M., Kim Y.-H., Kang S.-M., Lee I.-J. Ameliorative symbiosis of en- dophyte (Penicillium funiculosum LHL06) under salt stress elevated plant growth of Glycine max L. Plant Physiol Biochem. 2011. Vol. 49, Is. 8. P. 852– 861. https://doi.org/10.1016/j.plaphy.2011.03.005 38. Yasser M. M., Ahmed A. S. M., Osa- ma N. M., Nasr S. H. Solubilization of inorganic phosphate by phosphate solubilizing fungi isolated from Egyptian soils. J Biol Earth Sci. 2014. Vol. 4, № 1. P. 83–90. 39. Fenice M., Selbman L., Federici F., Vas- silev N. Application of encapsulated Penicillium variabile P16 in solubilization of rock phospha- te. Bioresource Technology. 2000. Vol. 73, Is. 2. P. 157–162. https://doi.org/10.1016/S0960-8524(99) 00150-9 40. Crognale S., Petruccioli M., Fenice M., Fe- derici F. Fed-batch gluconic acid production from Penicillium variabile P16 under different feeding strategies. Enzyme and Microbial Technology. 2008. Vol. 42, Is. 5. P. 445–449. https://doi.org/10.1016/ j.enzmictec.2008.01.002 41. Kanse O. S., Whitelaw-Weckert M., Ka- dam T. A., Bhosale H. J. Phosphate solubilization by stress-tolerant soil fungus Talaromyces funiculosus SLS8 isolated from the Neem rhizosphere. Ann Mi- crobiol. 2015. Vol. 65. P. 85–93. https://doi.org/10. 1007/s13213-014-0839-6 ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 32 42. El-Azouni I. M. Effect of phosphate solubi- lizing fungi on growth and nutrient uptake of soya- bean (Glycine max L.) plants. Journal of Applied Science Research. 2008. № 4. P. 592–598. 43. Doilom M., Guo J.-W., Phookamsak R., Mortimer P. E., Karunarathna S. C., Dong W. … Xu J.-C. Screening of Phosphate-Solubilizing Fungi From Air and Soil in Yunnan, China: Four Novel Species in Aspergillus, Gongronella, Penicillium, and Talaromyces. Front Microbiol. 2020. Vol. 11. https://doi.org/10.3389/fmicb.2020.585215 44. Suraby E. J., Agisha V. N., Dhandapani S., Sng Y. H., Lim S. H., Naqvi N. I. … Park B. S. Plant growth promotion under phosphate deficiency and improved phosphate acquisition by new fungal strain, Penicillium olsonii TLL1. Front Microbiol. 2023. Vol. 14. https://doi.org/10.3389/fmicb.2023. 1285574 45. Takeda M., Knight J. D. Enhanced solubili- zation of rock phosphate by Penicillium bilaiae in pH-buffered solution culture. Can J Microbiol. 2006. Vol. 51, № 11. P. 1121–1129. https://doi.org/ 10.1139/w06-074 46. Qiao H., Sun X.-R., Wu X.-Q., Li G.-E., Wang Z., Li D.-W. The phosphate-solubilizing abi- lity of Penicillium guanacastense and its effects on the growth of Pinus massoniana in phosphate-limi- ting conditions. Biol Open. 2019. Vol. 8, Is. 11. https://doi.org/10.1242/bio.046797 47. Henri F., Laurette N. N., Ghislain N. N., Vanessa T. T. G., Virginie T. I. A., Dieudonné N. Rock phosphate solubilisation by strains of Penicil- lium spp. isolated from farm and forest soils of three agro ecological zones of Cameroon. American Jour- nal of Agriculture and Forestry. 2014. Vol. 2, Is. 2. P. 25–32. https://doi.org/10.11648/j.ajaf.20140202.12 48. Mahadevamurthy M., Channappa T. M, Si- dappa M., Raghupathi M. S, Nagaraj A. K. Isolation of phosphate solubilizing fungi from rhizosphere soil and its effect on seed growth parameters of dif- ferent crop plants. Journal of Applied Biology & Biotechnology. 2016. Vol. 4, Is. 6. P. 22–26. http:// dx.doi.org/10.7324/JABB.2016.40604 49. Elias F., Woyessa D., Muleta D. Phosphate solubilization potential of rhizosphere fungi isolated from plants in Jimma Zone, Southwest Ethiopia. Int J Microbiol. 2016. P. 1–11. http://dx.doi.org/10. 1155/2016/5472601 50. Omar S. A. The role of rock phosphate so- lubilizing fungi and vesicular arbuscular mycorrhiza (VAM) in growth of wheat plants fertilized with rock phosphate. World J Microbiol Biotechnol. 1998. Vol. 14. P. 211–219. http://dx.doi.org/10.1023/ A:1008830129262 51. Khan M. S., Zaidi A., Wani P. A. Role of phosphate solubilising microorganisms in sustai- nable agriculture. E. Lictfouse, M. Navarrete, P. Debaeke, S. Véronique, C. Alberola (Eds.). Sus- tainable Agriculture. Dordrecht: Springer, 2009. P. 551–570. https://doi.org/10.1007/978-90-481- 2666-8_34 52. Nannipieri P., Giagnoni L., Landi L., Renel- la G. Role of phosphatase enzymes in soil. E. Bu- nemann, A. Oberson, E. Frossard (Eds.). Phospho- rus in Action. Soil Biology. Vol. 26. Heidelberg : Springer, 2011. P. 251–244. https://doi.org/10.1007/ 978-3-642-15271-9_9 53. Richardson A. E., Simpson R. J. Soil mi- croorganisms mediating phosphorus availability. Plant Physiol. 2011. Vol. 156. P. 989–996. https:// doi.org/10.1104/pp.111.175448 54. Rodriguez H., Fraga R., Gonzalez T., Ba- shan Y. Genetics of phosphate solubilization and its potential applications for improving plant growth-promoting bacteria. Plant Soil. 2006. Vol. 287. P. 15–21. https://doi.org/10.1007/s11104- 006-9056-9 55. Bashan Y., Kamnev A. A., de Bashan L. E. Tricalcium phosphate is inappropriate as a universal selection factor for isolating and testing phospha- te-solubilizing bacteria that enhance plant growth: a proposal for an alternative procedure. Biol Fertil Soils. 2013. Vol. 49. P. 465–479. https://doi.org/ 10.1007/s00374-012-0737-7 56. Шаховніна О. О., Надкернична О. В., Гор- баток А. В. Вплив грибів роду Penicillium, ізо- льованих з коренів сої, на симбіотичну систему «Glycine max – Bradyrhizobium japonicum». 2023. Вип. 38. С. 16–28. https://doi.org/10.35868/1997- 3004.38 57. Pikovskaya R. I. Mobilization of phospho- rus in soil in connection with vital activity of some microbial species. Microbiology. 1948. Vol. 17. P. 362–370. 58. Gupta R., Singal R., Shankar A., Ku- had R. C., Saxena R. K. A modified plate assay for screening phosphate solubilizing microorganisms. J Gen Appl Microbiol. 1994. Vol. 40. P. 255–260. https://doi.org/10.2323/JGAM.40.255 59. Nautiyal C. S. An efficient microbiological growth medium for screening phosphate solubilizing microorganisms. FEMS Microbiology Letters. 1998. Vol. 170. P. 265–270. https://doi.org/10.1016/ S0378-1097(98)00555-2 60. Premono M. E., Moawad A. M., Vlek P. L. G. Effect of phosphate-solubilizing Pseudomonas puti- da on the growth of maize and its survival in the rhizosphere. Indonesian Journal of Crop Science. 1996. Vol. 11. P. 13–23. 61. Волкогон В. В., Надкернична О. В., Ток- макова Л. М., Мельничук Т. М., Чайковська Л. О. Експериментальна ґрунтова мікробіологія: моно- ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41. 33 графія / за наук. ред. В. В. Волкогона. К. : Аграр- на наука, 2010. 464 с. 62. Nasr S. H., Mousa A. S. M., Yasser M. M., Marzouk M. A. Antagonistic potential of some pho- sphate solubilizing fungi against some phyto-patho- genic fungi. Beni-Suef University Journal of Basic and Applied Sciences. 2021. Vol. 10. 70. https://doi. org/10.1186/s43088-021-00159-y 63. Collavino M. M., Sansberro P. A., Mrogin- ski L. A., Aguilar O. M. Comparison of in vitro so- lubilization activity of diverse phosphate-solubili- zing bacteria native to acid soil and their ability to promote Phaseolus vulgaris growth. Biol Fertil Soils. 2010. Vol. 46. P. 727–738. https://doi.org/ 10.1007/s00374-010-0480-x Отримано: 21.02.2025 Прийнято до друку: 25.04.2025 Опубліковано онлайн: 17.09.2025 ISSN 1997-3004 Сільськогосподарська мікробіологія. 2025. Вип. 41.
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spelling oai:ojs2.smic.in.ua:article-5362026-07-22T10:10:52Z PHOSPHATE-MOBILISING PROPERTIES OF FUNGI OF THE GENUS PENICILLIUM ISOLATED FROM SOYBEAN HISTOSPHERE ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ Шаховніна, О. О. Надкернична, О. В. Пищур, І. М. endophytic fungi of soybean, PSF (phosphate solubilising fungi), inorganic phosphate dissolution, organic phosphate mineralisation, phosphatase гриби-ендофіти сої, PSF (гриби, які розчиняють фосфати), розчинення неорганічних фосфатів, мінералізація органічних фосфатів, фосфатаза Objective. To research the ability of fungi of the genus Penicillium, isolated from the histosphere of soybean plants, release phosphorus from mineral and organic phosphates, study their effect on the general phosphorus content in plant shoots. Methods. Microbiological (cultivation of the tested fungi on Pikovska’s medium and its modifications, Czapek-Dox agar with tricalcium phosphate or phenolphthalein phosphate, wort agar), vegetation experiment (content determination of general phosphorus in the aboveground mass of soybean plants), statistical. Results. The use of three insoluble phosphates in Pikovska medium showed that the tested fungi dissolve to varying degrees Са3(РО4)2 and are unable to dissolve AlPO4 and FePO4. On the seventh day of cultivation, clearly visible zones of enlightenment were formed around the colonies of P. funiculosum 20312 and P. variabile 20173, with phosphate dissolution indexes of 1.17 and 1.18, respectively. When cultivating fungi on Pikovska medium with the addition of bromophenol blue dye in P. funiculosum 20312 and P. variabile 20173, the medium quickly changed colour from green to yellow, indicating the diffusion of organic acids produced by the fungi into the agar. Starting from the twelfth day of the experiment, the environment around the colonies of fungi P. glauco-lanosum 20401 also acquired a rich yellow colour and the halo zones formation was observed. The presence of phosphatase activity was demonstrated for all the tested fungi. The tested strains of fungi had a positive effect on the general phosphorus content in the dry matter of soybean shoots, this indicator increased notably in the variant with the use of P. funiculosum 20312 — 0.751 % against 0.643 % in the control variant. Conclusions. The tested fungi of the genus Penicillium, isolated from surface-sterilised roots of soybean plants, are capable of releasing phosphorus by dissolving inorganic and mineralising organic phosphates, and have a positive effect on the content of general phosphorus in soybean shoots. Мета. Дослідити здатність грибів роду Penicillium, ізольованих із гістосфери рослин сої, вивільняти фосфор із мінеральних та органічних фосфатів, вивчити їхній вплив на вміст загального фосфору в пагонах рослин. Методи. Мікробіологічні (культивування досліджуваних грибів на середовищі Піковської та його модифікаціях, агарі Чапека-Докса із додаванням трикальційфосфату або фенолфталеїнфосфату, сусловому агарі), вегетаційного досліду (визначення вмісту загального фосфору в надземній масі рослин сої), статистичні. Результати. Використання трьох нерозчинних фосфатів у складі середовища Піковської показало, що досліджувані гриби різною мірою розчиняють Са3(РО4)2 і не здатні розчиняти AlPO4 та FePO4. На сьому добу культивування навколо колоній P. funiculosum 20312 і P. variabile 20173 утворювалися добре помітні зони просвітлення, індекси розчинення фосфату становили 1,17 і 1,18 відповідно. За культивування грибів на середовищі Піковської з додаванням бромфенолового синього барвника у варіантах P. funiculosum 20312 і P. variabile 20173 середовище швидко змінювало колір з зеленого на жовтий, що свідчить про дифузію в агар органічних кислот, продукованих грибами. Починаючи з дванадцятої доби досліду, середовище навколо колоній гриба P. glauco-lanosum 20401 також набувало насиченого жовтого кольору і було відзначено появу гало-зон. Для всіх досліджуваних грибів показано наявність фосфатазної активності. Досліджувані штами грибів позитивно впливали на вміст загального фосфору в сухій речовині пагонів сої, достовірно цей показник підвищувався у варіанті із застосуванням P. funiculosum 20312 — 0,751 % проти 0,643 % у контрольному варіанті. Висновки. Досліджувані гриби роду Penicillium, ізольовані з поверхнево стерилізованих коренів рослин сої, здатні вивільняти фосфор за рахунок розчинення неорганічних і мінералізації органічних фосфатів, позитивно впливають на вміст загального фосфору в пагонах рослин сої. Institute of Agrocultural Microbiology and Agro-industrial Manufacture of NAAS of Ukraine 2025-05-15 Article Article Рецензована Стаття application/pdf https://smic.in.ua/index.php/journal/article/view/536 10.35868/1997-3004.41.19-33 Agricultural microbiology; Vol. 41 (2025): Agriciltural microbiology; 19-33 Сільськогосподарська мікробіологія; Том 41 (2025): Сільськогосподарська мікробіологія; 19-33 1997-3004 10.35868/1997-3004.41 en https://smic.in.ua/index.php/journal/article/view/536/605 Авторське право (c) 2025 O. О. Shakhovnina, О. V. Nadkernychna, І. M. Pyshchur https://creativecommons.org/licenses/by/4.0
spellingShingle гриби-ендофіти сої
PSF (гриби
які розчиняють фосфати)
розчинення неорганічних фосфатів
мінералізація органічних фосфатів
фосфатаза
Шаховніна, О. О.
Надкернична, О. В.
Пищур, І. М.
ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ
title ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ
title_alt PHOSPHATE-MOBILISING PROPERTIES OF FUNGI OF THE GENUS PENICILLIUM ISOLATED FROM SOYBEAN HISTOSPHERE
title_full ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ
title_fullStr ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ
title_full_unstemmed ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ
title_short ФОСФАТМОБІЛІЗУВАЛЬНІ ВЛАСТИВОСТІ ГРИБІВ РОДУ PENICILLIUM, ВИДІЛЕНИХ З ГІСТОСФЕРИ СОЇ
title_sort фосфатмобілізувальні властивості грибів роду penicillium, виділених з гістосфери сої
topic гриби-ендофіти сої
PSF (гриби
які розчиняють фосфати)
розчинення неорганічних фосфатів
мінералізація органічних фосфатів
фосфатаза
topic_facet endophytic fungi of soybean
PSF (phosphate solubilising fungi)
inorganic phosphate dissolution
organic phosphate mineralisation
phosphatase
гриби-ендофіти сої
PSF (гриби
які розчиняють фосфати)
розчинення неорганічних фосфатів
мінералізація органічних фосфатів
фосфатаза
url https://smic.in.ua/index.php/journal/article/view/536
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