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苏云金芽孢杆菌库尔斯塔克亚种HBK-51产生的一种耐热碱性几丁质酶

Production of a Thermostable and Alkaline Chitinase by Bacillus thuringiensis subsp. kurstaki Strain HBK-51.

作者信息

Kuzu Secil Berna, Güvenmez Hatice Korkmaz, Denizci Aziz Akin

机构信息

Biotechnology & Molecular Biology Division, Department of Biology, Cukurova University, 01330 Adana, Turkey.

出版信息

Biotechnol Res Int. 2012;2012:135498. doi: 10.1155/2012/135498. Epub 2012 Dec 13.

Abstract

This paper reports the isolation and identification of chitinase-producing Bacillus from chitin-containing wastes, production of a thermostable and alkaline chitinasese, and enzyme characterization. Bacillus thuringiensis subsp. kurstaki HBK-51 was isolated from soil and was identified. Chitinase was obtained from supernatant of B. thuringiensis HBK-51 strain and showed its optimum activity at 110°C and at pH 9.0. Following 3 hours of incubation period, the enzyme showed a high level of activity at 110°C (96% remaining activity) and between pH 9.0 and 12.0 (98% remaining activity). Considering these characteristics, the enzyme was described as hyperthermophile-thermostable and highly alkaline. Two bands of the enzyme weighing 50 and 125 kDa were obtained following 12% SDS-PAGE analyses. Among the metal ions and chemicals used, Ni(2+) (32%), K(+) (44%), and Cu(2+) (56%) increased the enzyme activity while EDTA (7%), SDS (7%), Hg(2+) (11%), and ethyl-acetimidate (20%) decreased the activity of the enzyme. Bacillus thuringiensis subsp. kurstaki HBK-51 is an important strain which can be used in several biotechnological applications as a chitinase producer.

摘要

本文报道了从含几丁质废料中分离和鉴定产几丁质酶的芽孢杆菌、一种耐热且耐碱的几丁质酶的生产以及酶的特性。苏云金芽孢杆菌库尔斯塔克亚种HBK - 51从土壤中分离并鉴定。几丁质酶从苏云金芽孢杆菌HBK - 51菌株的上清液中获得,在110°C和pH 9.0时表现出最佳活性。经过3小时的孵育期后,该酶在110°C时表现出高活性(剩余活性96%),在pH 9.0至12.0之间(剩余活性98%)。考虑到这些特性,该酶被描述为嗜热超稳定且高度耐碱。经过12% SDS - PAGE分析后获得了两条分子量分别为50 kDa和125 kDa的酶带。在所使用的金属离子和化学物质中,Ni(2+)(32%)、K(+)(44%)和Cu(2+)(56%)提高了酶活性,而EDTA(7%)、SDS(7%)、Hg(2+)(11%)和乙基亚胺酯(20%)降低了酶活性。苏云金芽孢杆菌库尔斯塔克亚种HBK - 51是一种重要的菌株,作为几丁质酶生产者可用于多种生物技术应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a7d/3532916/db7dd7449051/BTRI2012-135498.001.jpg

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