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首页> 外文期刊>FEMS Microbiology Letters >Identification of strong promoter elements of Mycobacterium smegmatis and their utility for foreign gene expression in mycobacteria
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Identification of strong promoter elements of Mycobacterium smegmatis and their utility for foreign gene expression in mycobacteria

机译:耻垢分枝杆菌强启动子元件的鉴定及其在分枝杆菌中外源基因表达中的用途

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摘要

The isolation of elements driving high-level expression of foreign genes in mycobacteria would significantly aid characterization of mycobacterial antigens and recombinant vaccine development. Mycobacterium smegmatis is a widely employed host for recombinant mycobacterial gene expression. This report describes the identification of strong promoter elements of M. smegmatis. Fluorescence-activated cell sorting was employed to isolate DNA fragments permitting high-level expression of the Aequorea victoria green fluorescent protein within recombinant M. smegmatis. Ten postulated M. smegmatis promoters were identified which showed activity two to six times that of the strong beta-lactamase promoter of Mycobacterium fortuitum. The utility of one of these promoters for the over-expression of foreign genes in mycobacteria was demonstrated by the efficient purification of the Mycobacterium leprae 35-kDa antigen from recombinant M. smegmatis. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved. [References: 17]
机译:分离驱动分枝杆菌中外源基因高水平表达的元件将大大有助于分枝杆菌抗原的表征和重组疫苗的开发。耻垢分枝杆菌是重组分枝杆菌基因表达的广泛使用的宿主。该报告描述了耻垢分枝杆菌强启动子元件的鉴定。使用荧光激活的细胞分选来分离DNA片段,以允许在重组耻垢分枝杆菌内高水平表达维多利亚水母绿色荧光蛋白。鉴定出十个假定的耻垢分枝杆菌启动子,它们显示出比分枝杆菌的强β-内酰胺酶启动子强两倍到六倍的活性。通过从重组耻垢分枝杆菌有效纯化麻风分枝杆菌35-kDa抗原,证明了这些启动子之一在分枝杆菌中外源基因的过表达。 (C)2003年欧洲微生物学会联合会。由Elsevier Science B.V.保留所有权利。 [参考:17]

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