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利用大丽花块茎提取物生产马克斯克鲁维酵母菊粉酶。

Production of inulinase from Kluyveromyces marxianus using dahlia tuber extract.

机构信息

Department of Applied Microbiology and Biotechnology, Dr. Hari Singh Gour University , Sagar, M.P. 470003 , India.

出版信息

Braz J Microbiol. 2012 Jan;43(1):62-9. doi: 10.1590/S1517-83822012000100007. Epub 2012 Jun 1.

Abstract

Various carbon sources were evaluated for production of inulinase by yeast, Kluyveromyces marxianus MTCC 3995. Highest inulinase activity was observed with Dahlia extract (25.3 nkat mL(-1)) as carbon source. The enzyme activity was 1.4 folds higher than that observed in media containing pure chicory inulin (17.8 nkat mL(-1)). The yeast showed good growth on a simple medium containing dahlia extract (20% w/v) and yeast extract (2%w/v) as carbon and nitrogen source respectively, in 96 h. at 28°C and 120 rpm. Lowest inulinase yield (4.8 nkat mL(-1)) was seen in the medium containing glucose as C-source. Although varied inulinase levels were noticed on different C- sources, Inulinase: Sucrase (I/S) ratios were noticed to be similar. Among various protein sources tested, yeast extract was found to be the best source followed by beef extract (17.9 nkat mL(-1)) and peptone (13.8 nkat mL(-1)). The enzyme was optimally active at pH (4.0) and 50°C. TLC analysis of end product revealed that inulinase hydrolyzed inulin exclusively into fructose. Results suggest that the dahlia extract induced exoinulinase synthesis in Kluyveromyces marxianus and can be utilized as a potential substrate for inulinase production.

摘要

各种碳源被评估用于酵母 Kluyveromyces marxianus MTCC 3995 生产菊粉酶。以大丽花提取物(25.3 nkat mL(-1))作为碳源时,观察到最高的菊粉酶活性。该酶活性比含有纯菊苣菊粉(17.8 nkat mL(-1))的培养基中观察到的活性高 1.4 倍。该酵母在含有大丽花提取物(20%w/v)和酵母提取物(2%w/v)的简单培养基中表现出良好的生长,在 28°C 和 120 rpm 下 96 h 后即可生长。以葡萄糖作为 C 源时,观察到最低的菊粉酶产量(4.8 nkat mL(-1))。虽然在不同的 C 源上观察到不同的菊粉酶水平,但观察到菊粉酶:蔗糖酶(I/S)比值相似。在所测试的各种蛋白质源中,发现酵母提取物是最佳来源,其次是牛肉提取物(17.9 nkat mL(-1))和蛋白胨(13.8 nkat mL(-1))。该酶在 pH(4.0)和 50°C 时活性最佳。末端产物的 TLC 分析表明,菊粉酶将菊粉专一地水解成果糖。结果表明,大丽花提取物诱导 Kluyveromyces marxianus 合成外切菊粉酶,可作为菊粉酶生产的潜在底物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3b7/3768966/9d83ec389ba1/bjm-43-62-g001.jpg

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