SCHIZOPHYLLUM COMMUNE AS A PROMISING EXO-POLYGALACTURONASE PRODUCER

Authors

DOI:

https://doi.org/10.31073/foodresources2025-25-09

Keywords:

basidiomycetes, Schizophyllum, pectinolytic enzymes, enzymatic activity, polygalacturonase, surface cultivation, liquid nutrient media

Abstract

Subject. Juices are products with high nutritional and commercial value, but their production is complicated by the presence of pectic compounds. Exopolygalacturonases are often used to decompose such compounds. Among the potential producers of exopolygalacturonases, the basidiomycete Schizophyllum commune is promising, as it has a developed system of extracellular enzymes and is capable of degrading plant cell wall components. Purpose. The aim of the study was to investigate the synthesis of exopolygalacturonase by S. commune strains in submerged culture. Methods. The objects of research were three strains of S. commune(S. commune 335, S. commune 1759 and S. commune 1770), obtained from The Mushroom Culture Collection of the M.G. Kholodny Institute of Botany of the NAS of Ukraine. Cultivation was carried out in glucose-peptone-yeast, synthetic media and modified Norcrans medium in static mode at a temperature of 28±1°C for 14 days. At the end of cultivation, the biomass yield was determined gravimetrically; the amount of reducing substances and proteins was determined spectrophotometrically. Statistical data processing was performed using the Duncan test. Results. The highest activity was demonstrated by S. commune 1759 strain on Norcrans medium (494.4±72.9 units/dm3), while strains 335 and 1770 were characterized by lower activity. The maximum specific activity (6.48±0.26 units/gprotein) was also found in strain 1759, and the highest synthesis productivity was found in strain 335 on synthetic medium (1510.5±227.4 units/gBM). The lowest activity values were observed in glucose-peptone-yeast medium, while Norcrans medium caused the maximum values. Scope of the results. The results obtained indicate the need for further studies of strains S. commune 335 and S. commune 1759 to optimize the yield of exopolygalacturonase and its application in the food industry.

Downloads

Download data is not yet available.

References

Sharma, H. P., Patel, H., Sugandha. (2017). Enzymatic added extraction and clarification of fruit juices – A review. Critical reviews in food science and nutrition, 57(6), 1215–1227. https://doi.org/10.1080/10408398.2014.977434.

Mosaad Khattab, A. (2022). The Microbial Degradation. Pectins: the new-old polysaccharides, 83. https://doi.org/10.5772/intechopen.100247.

Satapathy, S., Rout, J. R., Kerry, R. G., Thatoi, H., Sahoo, S. L. (2020). Biochemical prospects of various microbial pectinase and pectin: an approachable concept in pharmaceutical bioprocessing. Frontiers in Nutrition, 7, 117. https://doi.org/10.3389/fnut.2020.00117.

Junior, A. N., Mansoldo, F. R. P., Godoy, M. G., Firpo, R. M., Cedrola, S. M. L., Vermelho, A. B. (2021). Production of an endo-polygalacturonase from Fusarium proliferatum isolated from agro-industrial waste. Biocatalysis and Agricultural Biotechnology, 38, 102199. https://doi.org/10.1016/j.bcab.2021.102199.

Nighojkar, A., Patidar, M. K., Nighojkar, S. (2019). Pectinases: production and applications for fruit juice beverages. Processing and sustainability of beverages (pp. 235–273). Woodhead Publishing. https://doi.org/10.1016/B978-0-12-815259-1.00008-2.

Amin, F., Mohsin, A., Bhatti, H. N., Bilal, M. (2020). Production, thermodynamic characterization, and fruit juice quality improvement characteristics of an exo-polygalacturonase from Penicillium janczewskii. Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics, 1868 (5), 140379. https://doi.org/10.1016/j.bbapap.2020.140379.

Almowallad, S. A., Alshammari, G. M., Alsayadi, M. M., Aljafer, N., Al-Sanea, E. A., Yahya, M. A., Al-Harbi, L. N. (2022). Partial purification and characterization of exo-polygalacturonase produced by Penicillium oxalicum AUMC 4153. Life, 12 (2), 284. https://doi.org/10.3390/life12020284.

Zhu, N., Liu, J., Yang, J., Lin, Y., Yang, Y., Ji, L., Li, M., Yuan, H. (2016). Comparative analysis of the secretomes of Schizophyllum commune and other wood-decay basidiomycetes during solid-state fermentation reveals its unique lignocellulose-degrading enzyme system. Biotechnology for biofuels, 9 (1), 42. https://doi.org/10.1186/s13068-016-0461-x.

Park, Y. J., Jeong, Y. U., Kong, W. S. (2018). Genome sequencing and carbohydrate-active enzyme (CAZyme) repertoire of the white rot fungus Flammulina elastica. International journal of molecular sciences, 19 (8), 2379. https://doi.org/10.3390/ijms19082379.

Ruiz-Dueñas, F. J., Barrasa, J. M., Sánchez-García, M., Camarero, S., Miyauchi, S., Serrano, A., Linde, D., Babiker, R., Drula, E., Ayuso-Fernández, I., Pacheco, R., Padilla, G., Ferreira, P., Barriuso, J., Kellner, H., Castanera, R., Alfaro, M., Ramírez, L., Pisabarro, A.G., Riley, R., Kuo, A., Andreopoulos, W., LaButti, K., Pangilinan, J., Tritt, A., Lipzen, A., He, G., Yan, M., Ng, V., Grigoriev, I.V., Cullen, D., Martin, F., Rosso, M.-N., Henrissat, B., Hibbett, D., Martínez, A.T. (2021). Genomic analysis enlightens Agaricales lifestyle evolution and increasing peroxidase diversity. Molecular biology and evolution, 38(4), 1428–1446. https://doi.org/10.1093/molbev/msaa301.

Amin, F., Bhatti, H. N., Bilal, M., Asgher, M. (2017). Multiple parameter optimizations for enhanced biosynthesis of exo-polygalacturonase enzyme and its application in fruit juice clarification. International Journal of Food Engineering, 13 (2), 20160256. https://doi.org/10.1515/ijfe-2016-0256.

Mehmood, T., Saman, T., Asgher, M., Irfan, M., Anwar, Z., Nadeem, F., & Siddiqa, A. (2019). Optimization of cultural parameters for pectin methylestrase and polygalacturonase production from Schizophyllum commune in solid state fermentation. Bangladesh Journal of Botany, 48 (1), 65–74. https://doi.org/10.3329/bjb.v48i1.47417.

Bisko, N., Lomberg, M., Mykchaylova, O., & Mytropolska, N. (2020). IBK Mushroom Culture Collection. Version 1.2. The IBK Mu-shroom Culture Collection of the M.G. Kholodny Institute of Botany. M. G. Kholodny Institute of Botany. https://doi.org/10.15468/dzdsqu.

Bukhalo A. S. (1988) Higher edible basidiomycetes in pure culture. Kyiv: Naukova Dumka, 144.

Lomberg, M., Krupodorova, T., Krasinko, V., & Mykchaylova, О. (2023). The antibacterial activity of culture filtrates and mycelia of selected strains of macromycetes from the genus Hericium. Botanica Serbica, 47 (2), 241–249. https://doi.org/10.2298/BOTSERB2302241L.

Wood, I. P., Elliston, A., Ryden, P., Bancroft, I., Roberts, I. N., & Waldron, K. W. (2012). Rapid quantification of reducing sugars in biomass hydrolysates: Improving the speed and precision of the dinitrosalicylic acid assay. Biomass and Bioenergy, 44, 117–121. https://doi.org/10.1016/j.biombioe.2012.05.003.

Lowry, O. H., Rosebrough, N. J., Farr, A. L., Randall, R. J. (1951). Protein measurement with the Folin phenol reagent. 193 (1). 265–275.

Gomes, E., Leite, R. S. R., Da Silva, R., Silva, D. (2009). Purification of an exopolygalacturonase from Penicillium viridicatum RFC3 produced in submerged fermentation. International journal of microbiology, 2009 (1), 631942. https://doi.org/10.1155/2009/631942.

Dagbagli, S., Goksungur, Y. (2008). Optimization of ß-galactosidase production using Kluyveromyces lactis NRRL Y-8279 by response surface methodology. Electronic Journal of Biotechnology, 11 (4). https://doi.org/10.2225/vol11/issue4-fulltext-12.

Bisswanger, H. (2014). Enzyme assays. Perspectives in Science, 1 (1–6), 41–55. https://doi.org/10.1016/j.pisc.2014.02.005.

Sethi, B. K., Nanda, P. K., Sahoo, S. (2016). Enhanced production of pectinase by Aspergillus terreus NCFT 4269.10 using banana peels as substrate. 3 Biotech, 6 (1), 36. https://doi.org/10.1007/s13205-015-0353-y.

Boakye, S. O., Zakpaa, H. D. (2025). Bioprocess optimization for pectinase enzymes synthesized from fungal species under solid-state fermentation conditions. https://doi.org/10.20944/preprints202501.1905.v2.

Mukhopadhyay, D., Bhattacharyya, R., Bhattacharya, S., Alnafisi, B. K. (2024). Valorisation of Citrus limetta peel for Aspergillus terreus FP6 mediated pectinase fermentation and application in grape juice clarification. Journal of King Saud University-Science, 36 (10), 103454. https://doi.org/10.1016/j.jksus.2024.103454.

Begum, G., Munjam, S. (2021). Carbon and nitrogen sources effect on pectinase synthesis by Aspergillus niger under submerged fermentation. Biosciences Biotechnology Research Asia, 18 (1), 185–195. http://doi.org/10.13005/bbra/2906.

Mat Jalil, M. T., Zakaria, N. A., Salikin, N. H., & Ibrahim, D. (2023). Assessment of cultivation parameters influencing pectinase production by Aspergillus niger LFP-1 in submerged fermentation. Journal of Genetic Engineering and Biotechnology, 21 (1), 45. https://doi.org/10.1186/s43141-023-00510-z.

Khatri, B. P., Bhattarai, T., Shrestha, S., Maharjan, J. (2015). Alkaline thermostable pectinase enzyme from Aspergillus niger strain MCAS2 isolated from Manaslu Conservation Area, Gorkha, Nepal. Springer Plus, 4 (1), 488. https://doi.org/10.1186/s40064-015-1286-y.

Jalil, M. T. M., Ibrahim, D. (2021). Partial purification and characterisation of pectinase produced by Aspergillus niger LFP-1 grown on pomelo peels as a substrate. Tropical life sciences research, 32 (1), 1. https://doi.org/10.21315/tlsr2021.32.1.1.

Published

2025-12-22

How to Cite

Zubyk, P., Klechak, I., & Linovytska, V. (2025). SCHIZOPHYLLUM COMMUNE AS A PROMISING EXO-POLYGALACTURONASE PRODUCER. FOOD RESOURCES, 13(25), 83–90. https://doi.org/10.31073/foodresources2025-25-09

Issue

Section

Технічні науки