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鱼腥藻7120菌株中一个渗透压响应基因的调控

Regulation of an osmoticum-responsive gene in Anabaena sp. strain PCC 7120.

作者信息

Schwartz S H, Black T A, Jäger K, Panoff J M, Wolk C P

机构信息

MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824, USA.

出版信息

J Bacteriol. 1998 Dec;180(23):6332-7. doi: 10.1128/JB.180.23.6332-6337.1998.

Abstract

Salt-induced genes in the cyanobacterium Anabaena sp. strain PCC 7120 were identified by use of a Tn5-based transposon bearing luxAB as a reporter. The genomic sequence adjacent to one site of insertion of the transposon was identical in part to the sequence of the lti2 gene, which was previously identified in a differential screen for cold-induced transcripts in Anabaena variabilis. The lti2-like gene was induced by sucrose and other osmotica and by low temperature, in addition to salt. Regulatory components necessary for the induction of this gene by osmotica were sought by a further round of transposon mutagenesis. One mutant that displayed reduced transcriptional activity of the lti2-like gene in response to exposure to osmotica had an insertion in an open reading frame, which was denoted orrA, whose predicted product showed sequence similarity to response regulators from two-component regulatory systems. The corresponding mutation was reconstructed and was shown, like the second-site transposon mutation, to result in reduced response to osmotic stress. Induction of the lux reporter gene by osmotica was restored by complementation with a genomic fragment containing the entire open reading frame for the presumptive response regulator, whereas a fragment containing a truncated copy of the open reading frame for the response regulator did not complement the mutation.

摘要

利用携带luxAB作为报告基因的基于Tn5的转座子,鉴定了蓝藻鱼腥藻PCC 7120菌株中盐诱导基因。转座子插入位点之一附近的基因组序列部分与lti2基因的序列相同,lti2基因先前是在对多变鱼腥藻中冷诱导转录本的差异筛选中鉴定出来的。除了盐之外,lti2样基因还受蔗糖和其他渗透压物质以及低温诱导。通过新一轮的转座子诱变寻找渗透压物质诱导该基因所需的调控成分。一个在暴露于渗透压物质时显示lti2样基因转录活性降低的突变体,其在一个开放阅读框中有插入,该开放阅读框被命名为orrA,其预测产物与双组分调控系统中的应答调节子显示出序列相似性。重建了相应的突变,结果表明,与第二位点转座子突变一样,该突变导致对渗透胁迫的反应降低。通过用包含假定应答调节子完整开放阅读框的基因组片段进行互补,恢复了渗透压物质对lux报告基因的诱导作用,而包含应答调节子开放阅读框截短拷贝的片段不能互补该突变。

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