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Characterization and Optimization of Fungal L-Asparaginase Isolated From Soil and Medicinal Plants
Author(s) -
S. Ranjini Priya,
AS Subhashini
Publication year - 2022
Publication title -
journal of pure and applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.149
H-Index - 16
eISSN - 2581-690X
pISSN - 0973-7510
DOI - 10.22207/jpam.16.1.43
Subject(s) - asparaginase , asparagine , acrylamide , chemistry , enzyme , polyacrylamide gel electrophoresis , plant use of endophytic fungi in defense , nitrogen , enzyme assay , chromatography , food science , biochemistry , biology , botany , lymphoblastic leukemia , organic chemistry , monomer , genetics , leukemia , polymer
L-asparaginase is a therapeutic enzyme that converts L-asparagine into ammonia and L-aspartate. L-asparaginase is used to treat acute lymphoblastic leukaemia. In food manufacturing industries, it is used to inhibit the acrylamide formation. The current investigation has been performed to isolate L-asparaginase producing fungi from different medicinal plants and soil samples, through serial dilution. A total number of 15 fungal isolates were obtained from soil samples and 6 endophytic fungi isolated from medicinal plants. By performing screening of L-asparaginase 67% of positive isolates were obtained from endophytes and soil samples. Optimization of L-asparaginase production was performed for parameters such as pH, temperature, carbon and nitrogen source, and it was found that pH 6, 30˚C, 2 g of glucose, and 1 g of L-arginine is suitable for maximum enzyme production. By performing Sodium dodecyl sulphate polyacrylamide gel electrophoresis the molecular weight of an enzyme was determined to be approximately 11.2 kDa.

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