Department of Microbiology, Acharya Nagarjuna University , Guntur 522 510, A.P. , India.
Braz J Microbiol. 2009 Oct;40(4):725-33. doi: 10.1590/S1517-83822009000400002. Epub 2009 Dec 1.
Chitinase production by a terrestrial Streptomyces sp. ANU 6277 was studied under sub-merged fermentation. Chitinase production started after 24 h of incubation and reached maximum levels after 60 h of cultivation. A high level of chitinase activity was observed in the culture medium with pH 6 at 35°C. Culture medium amended with 1% chitin was found to be suitable for maximum production of chitinase. An optimum concentration of colloidal chitin for chitinase production was determined. Studies on the influence of additional carbon and nitrogen sources on chitinase production revealed that starch and yeast extract served as good carbon and nitrogen sources to enhance chitinase yield. Chitinase was purified from crude enzyme extract by single step gel filtration by Sephadex G-100. Purified chitinase of the strain exhibited a distinct protein band near 45 kDa by means of SDS-PAGE.
一株陆生链霉菌(Streptomyces sp. ANU 6277)的发酵产几丁质酶条件优化。该菌在发酵培养 24 h 后开始产酶,60 h 达到最大酶活。在 35℃、pH6 的条件下酶活最高。在添加 1%几丁质的发酵培养基中酶活最高。确定了几丁质酶产生的最佳胶体几丁质浓度。研究表明,额外的碳源和氮源对几丁质酶产量有影响,淀粉和酵母提取物是很好的碳源和氮源,可以提高几丁质酶的产量。通过 Sephadex G-100 凝胶过滤层析从粗酶提取物中纯化几丁质酶。SDS-PAGE 显示,纯化的几丁质酶在 45 kDa 附近有一条明显的蛋白条带。