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筛选南极链霉菌产生蛋白酶抑制剂。

Screening for production of proteinase inhibitors by Antarctic Streptomycetes.

机构信息

Medical University, Medical College "J. Filaretova" Sofia, Sofia, Bulgaria.

Faculty of Biology, Sofia University, Sofia, Bulgaria.

出版信息

J Basic Microbiol. 2018 Dec;58(12):1033-1042. doi: 10.1002/jobm.201800102. Epub 2018 Sep 20.

Abstract

Three out of 17 Streptomycetes strains - Streptomyces sp. 35 LBG09, Streptomyces sp. 36 LBG09, and Streptomyces sp. 39 LBG09, were selected based on the high production of proteinase inhibitors with trypsin serine proteinase activity. The strains were isolated from soil samples taken from the area around the Bulgarian station on Livingston Island, Antarctica. Biosynthesis of proteinase inhibitors by the promising strains started at different stages of their development but was generally not associated with the growth of the producers. Peak levels were reached in the stationary phase (96-120 h) of their cultivation. Inducing effects on strain development, biomass accumulation, and proteinase inhibitor biosynthesis were based on the composition of the nutrient medium: the polypeptones contained in Taguchi medium and glucose as a carbon source. The most productive out of the three strains was Streptomyces sp. 36 LBG09. Its maximum inhibitory activity was reached at 96 h in culturing media modified by three different carbon sources. The active proteinase inhibitor biosynthesis proceeded at pH values between 6.8 and 8.6 and the dynamics of production depended on the type of carbon source. Peak levels of extracellular protein and dry biomass were reached at 120 h in the stationary growth phase. The residual sugars were minimal at the end of the process when using soluble starch as a carbon source, and maximal when glucose was used.

摘要

基于对具有胰蛋白酶丝氨酸蛋白酶活性的蛋白酶抑制剂的高产量,从来自南极洲利文斯顿岛保加利亚站周围地区的土壤样本中选择了 17 株链霉菌菌株中的 3 株,即链霉菌 sp.35 LBG09、链霉菌 sp.36 LBG09 和链霉菌 sp.39 LBG09。这些菌株是从南极利文斯顿岛保加利亚站周围地区的土壤样本中分离出来的。有前途的菌株的蛋白酶抑制剂生物合成始于其发育的不同阶段,但通常与生产者的生长无关。在培养的静止阶段(96-120 小时)达到峰值。对菌株发育、生物量积累和蛋白酶抑制剂生物合成的诱导作用基于营养培养基的组成:Taguchi 培养基中的多肽和葡萄糖作为碳源。在三种不同碳源修饰的培养介质中,三种菌株中最具生产力的是链霉菌 sp.36 LBG09。其最大抑制活性在培养 96 小时时达到,在 pH 值为 6.8 到 8.6 之间进行活性蛋白抑制剂生物合成,生产动力学取决于碳源的类型。在静止生长阶段 120 小时时达到细胞外蛋白和干生物量的峰值。当使用可溶性淀粉作为碳源时,最终过程中的残留糖最小,而当使用葡萄糖时,残留糖最大。

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