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从酱油曲霉中分离的碱性蛋白酶的分离、特性鉴定及培养参数优化

Isolation, characterization and optimization of culture parameters for production of an alkaline protease isolated from Aspergillus tamarii.

作者信息

Anandan Dayanandan, Marmer William N, Dudley Robert L

机构信息

U.S. Department of Agriculture, Agricultural Research Service, Eastern Regional Research Center, Wyndmoor, PA 19038, USA.

出版信息

J Ind Microbiol Biotechnol. 2007 May;34(5):339-47. doi: 10.1007/s10295-006-0201-5. Epub 2007 Jan 24.

Abstract

Aspergillus tamarii expresses an extracellular alkaline protease that we show to be effective in removing hair from cattle hide. Large quantities of the enzyme will be required for the optimization of the enzymatic dehairing process so the growth conditions for maximum protease expression by A. tamarii were optimized for both solid-state culture on wheat bran and for broth culture. Optimal protease expression occurred, for both cultural media, at initial pH 9; the culture was incubated at 30 degrees C for 96 h using a 5% inoculum. The crude enzyme was isolated, purified and characterized using MALDI TOF TOF. The alkaline protease was homologous to the alkaline protease expressed by Aspergillus viridinutans.

摘要

溜曲霉可表达一种胞外碱性蛋白酶,我们发现该酶在去除牛皮毛发方面有效。为优化酶法脱毛工艺,将需要大量这种酶,因此针对溜曲霉在麦麸上的固态培养以及液体培养,对其最大程度表达蛋白酶的生长条件进行了优化。对于这两种培养基,在初始pH 9时都出现了最佳的蛋白酶表达;使用5%的接种量,在30℃下将培养物孵育96小时。使用基质辅助激光解吸电离飞行时间质谱仪(MALDI TOF TOF)对粗酶进行分离、纯化和表征。该碱性蛋白酶与绿褐曲霉表达的碱性蛋白酶同源。

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