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转座子Tn10依赖的大肠杆菌中lamB基因的表达

Transposon Tn10-dependent expression of the lamB gene in Escherichia coli.

作者信息

Brass J M, Manson M D, Larson T J

出版信息

J Bacteriol. 1984 Jul;159(1):93-9. doi: 10.1128/jb.159.1.93-99.1984.

Abstract

Among Tn10 insertions isolated in or near the malB region of Escherichia coli, one (zjb-729::Tn10) mapped between malK and lamB or late in malK and allowed MalT-independent expression of lamB. Tn10-dependent expression of a lamB-lacZ protein fusion was 25% of the expression of the fusion from the malK-lamB operon promoter in malTc constitutive strains. The maltoporin content of a strain carrying this Tn10 was about 20% that of a malTc malB+ strain. Transport of maltose at concentrations of below 10(-6) M was reduced about threefold. When maltoporin was present at about 50% of the level of malTc malB+ strains, maltose transport was largely restored. We conclude that maltoporin is not rate limiting for maltose transport in wild-type cells but becomes rate limiting when the ratio of maltoporin to other maltose transport components is reduced more than twofold.

摘要

在大肠杆菌malB区域内或其附近分离得到的Tn10插入突变体中,有一个(zjb - 729::Tn10)定位于malK和lamB之间,或者在malK下游,它能使lamB基因在不依赖MalT的情况下表达。在malTc组成型菌株中,lamB - lacZ蛋白融合体的Tn10依赖性表达是malK - lamB操纵子启动子驱动的融合体表达量的25%。携带此Tn10的菌株中麦芽糖孔蛋白的含量约为malTc malB +菌株的20%。浓度低于10(-6) M时麦芽糖的转运速率降低约三倍。当麦芽糖孔蛋白含量约为malTc malB +菌株水平的50%时,麦芽糖转运功能基本恢复。我们得出结论,在野生型细胞中麦芽糖孔蛋白不是麦芽糖转运的限速因素,但当麦芽糖孔蛋白与其他麦芽糖转运成分的比例降低超过两倍时,它就会成为限速因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dfa/215597/27ab76f1c756/jbacter00230-0102-a.jpg

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