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首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Intracellular alkaline proteases produced by thermoacidophiles: detection of protease heterogeneity by gelatin zymography and polymerase chain reaction (PCR)
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Intracellular alkaline proteases produced by thermoacidophiles: detection of protease heterogeneity by gelatin zymography and polymerase chain reaction (PCR)

机译:热嗜酸菌产生的细胞内碱性蛋白酶:通过明胶酶谱法和聚合酶链反应(PCR)检测蛋白酶异质性

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摘要

In this study 24 thermoacidophilic archeal and bacterial strains isolated from hot-springs and hot-soils were screened for their ability to produce intracellular alkaline proteases. The protease activities of the strains, based on azocasein hydrolysis, showed a variation from 0.6 to 5.1 U. The cell extracts of three most potent producers were further examined and it was found that their proteases exhibited maximum activity at 60-70 degreesC and showed a pH Optimum over a range of pH 7.0-8.5. Gelatin zymography revealed that two of the selected archeal strains produced multiple active SDS-resistant proteases. On the other hand, PCR amplification of alkaline serine protease gene sequences of total DNA from all isolates yielded four distinct amplification fragments of 650, 450, 400 and 300 bp, which might have been derived from different serine protease genes. (C) 2002 Elsevier Science Ltd. All rights reserved. [References: 19]
机译:在这项研究中,从温泉和热土中分离出的24种嗜热古菌和细菌菌株被筛选出它们产生细胞内碱性蛋白酶的能力。基于偶氮酪蛋白水解的菌株的蛋白酶活性显示出从0.6到5.1 U的变化。进一步检查了三个最有力的生产者的细胞提取物,发现它们的蛋白酶在60-70摄氏度下表现出最大的活性并显示出pH在7.0-8.5范围内最佳。明胶酶谱分析表明,所选的两个古细菌菌株产生了多种活性的抗SDS的蛋白酶。另一方面,从所有分离物中的总DNA碱性丝氨酸蛋白酶基因序列的PCR扩增产生了650、450、400和300 bp的四个不同的扩增片段,这些片段可能源自不同的丝氨酸蛋白酶基因。 (C)2002 Elsevier ScienceLtd。保留所有权利。 [参考:19]

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