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在豌豆根瘤菌蚕豆生物变种中编码的一种类Fnr蛋白与苜蓿根瘤菌FixK具有结构和功能同源性。

An Fnr-like protein encoded in Rhizobium leguminosarum biovar viciae shows structural and functional homology to Rhizobium meliloti FixK.

作者信息

Colonna-Romano S, Arnold W, Schlüter A, Boistard P, Pühler A, Priefer U B

机构信息

University of Bielefeld, Faculty of Biology, Department of Genetics, Federal Republic of Germany.

出版信息

Mol Gen Genet. 1990 Aug;223(1):138-47. doi: 10.1007/BF00315806.

Abstract

A 1.9 kb DNA region of Rhizobium leguminosarum biovar viciae strain VF39 capable of promoting microaerobic and symbiotic induction of the Rhizobium meliloti fixN gene was identified by heterologous complementation. Sequence analysis of this DNA region revealed the presence of two complete open reading frames, orf240 and orf114. The deduced amino acid sequence of orf240 showed significant homology to Escherichia coli Fnr and R. meliloti FixK. The major difference between ORF240 and FixK is the presence of 21 N-terminal amino acids in ORF240 that have no counterpart in FixK. A similar protein domain is also present in E. coli Fnr and is essential for the oxygen-regulated activity of this protein. Analysis of the nucleotide sequence upstream of orf240 revealed a motif similar to the NtrA-dependent promoter consensus sequence, as well as two DNA regions resembling the Fnr consensus binding sequence. A Tn5-generated mutant in orf240 lost the ability to induce the R. meliloti fixN-lacZ fusion. Interestingly, this mutant was still capable of nitrogen fixation but showed reduced nitrogenase activity.

摘要

通过异源互补鉴定出了豌豆根瘤菌生物变种蚕豆菌株VF39中一个1.9 kb的DNA区域,该区域能够促进苜蓿根瘤菌fixN基因的微需氧和共生诱导。对该DNA区域的序列分析揭示了两个完整的开放阅读框,即orf240和orf114。orf240推导的氨基酸序列与大肠杆菌Fnr和苜蓿根瘤菌FixK具有显著同源性。ORF240与FixK的主要区别在于ORF240的N端有21个氨基酸在FixK中没有对应物。大肠杆菌Fnr中也存在类似的蛋白质结构域,并且对于该蛋白质的氧调节活性至关重要。对orf240上游核苷酸序列的分析揭示了一个类似于依赖NtrA的启动子共有序列的基序,以及两个类似于Fnr共有结合序列的DNA区域。orf240中由Tn5产生的突变体失去了诱导苜蓿根瘤菌fixN-lacZ融合的能力。有趣的是,该突变体仍然能够进行固氮,但固氮酶活性降低。

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