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利用从海洋环境中分离出的细菌发现角蛋白酶。

Discovery of keratinases using bacteria isolated from marine environments.

作者信息

Herzog Bastian, Overy David P, Haltli Bradley, Kerr Russell G

机构信息

Department of Chemistry, University of Prince Edward Island, 550 University Avenue, Charlottetown, PEI C1A 4P3, Canada; Nautilus Biosciences Canada, Duffy Research Center (NRC-INH) , 550 University Avenue, Charlottetown, PEI C1A 4P3, Canada.

Department of Chemistry, University of Prince Edward Island, 550 University Avenue, Charlottetown, PEI C1A 4P3, Canada; Department of Pathology and Microbiology, Atlantic Veterinary College, University of Prince Edward Island, 550 University Avenue, Charlottetown, PEI C1A 4P3, Canada; Nautilus Biosciences Canada, Duffy Research Center (NRC-INH) , 550 University Avenue, Charlottetown, PEI C1A 4P3, Canada.

出版信息

Syst Appl Microbiol. 2016 Feb;39(1):49-57. doi: 10.1016/j.syapm.2015.10.004. Epub 2015 Nov 9.

Abstract

Bacteria are important for the biodegradation of keratin. Thus, a workflow to isolate keratin-degrading bacteria utilizing an optimized azo-keratin assay was established. Deteriorated feather samples, collected in marine shoreline environments from the intertidal zone, yielded 50 unique bacterial isolates exhibiting keratin degradation when feather meal was supplied as keratin substrate. The majority of isolates, identified by 16S sequencing, belonged to genera previously reported to produce keratinases: Bacillus spp. (42%) and Stenotrophomonas spp. (40%). The remaining 18% represented the genera Alcaligenes, Chryseobacterium, Salinivibrio, Delftia, Stappia, and Microbacterium, genera not previously been associated with keratinase production. The workflow, also applied to 21 Bacilli from our in-house culture collection, additionally revealed four Bacilli with remarkable feather degradation potential. The industrial applicability of their associated keratinases was evaluated and the most active keratinase expressed in E. coli to confirm keratinase expression. Enriched keratinase fractions demonstrated activity up to 75°C and retained viability when stored lyophilized at 20°C for up to 200d.

摘要

细菌对角蛋白的生物降解很重要。因此,建立了一种利用优化的偶氮角蛋白测定法分离角蛋白降解细菌的工作流程。从潮间带海洋海岸线环境中收集的变质羽毛样本,以羽毛粉作为角蛋白底物时,产生了50株表现出角蛋白降解能力的独特细菌分离株。通过16S测序鉴定,大多数分离株属于先前报道的能产生角蛋白酶的属:芽孢杆菌属(42%)和嗜麦芽窄食单胞菌属(40%)。其余18%代表产碱菌属、金黄杆菌属、盐弧菌属、代尔夫特菌属、斯塔皮亚菌属和微杆菌属,这些属以前未与角蛋白酶生产相关联。该工作流程也应用于我们内部培养物保藏中心的21株芽孢杆菌,另外还发现了4株具有显著羽毛降解潜力的芽孢杆菌。评估了它们相关角蛋白酶的工业适用性,并在大肠杆菌中表达最活跃的角蛋白酶以确认角蛋白酶的表达。富集的角蛋白酶组分在高达75°C时仍具有活性,冻干后在20°C下保存长达200天仍保持活力。

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