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钼对棕色固氮菌固氮作用的转录调控

Transcriptional regulation of nitrogen fixation by molybdenum in Azotobacter vinelandii.

作者信息

Jacobson M R, Premakumar R, Bishop P E

出版信息

J Bacteriol. 1986 Aug;167(2):480-6. doi: 10.1128/jb.167.2.480-486.1986.

Abstract

Multiple genomic regions homologous to nifH were found in the diazotroph Azotobacter vinelandii. The nifHDK gene cluster, located on a 12.8-kilobase (kb) XhoI fragment and two additional XhoI fragments (7.4 and 8.4 kb) hybridized to a nifH-specific DNA template but the 7.4- and 8.4-kb fragments did not hybridize to nifD- or nifK-specific DNA probes. In vivo transcription of the nifHDK gene cluster was ammonia-repressible and required the presence of at least 50 nM molybdenum in the derepression medium. Three mRNA species were transcribed from the nifHDK gene cluster, a 4.2-kb transcript homologous to nifH-, nifD-, and nifK-specific DNA templates, a 2.6-kb transcript homologous to nifH- and nifD-specific DNA templates, and a 1.2-kb transcript homologous only to the nifH-specific DNA template. In strain CA11, a nifHDK deletion mutant, the nifHDK-specific transcripts were not produced and the strain was unable to grow in N-free medium in the presence of Na2MoO4 at concentrations of 50 nM or higher. However, at concentrations of 25 nM Mo or less, growth occurred in N-free medium. Under these conditions two nifH-homologous (but not nifD- or nifK-homologous) transcripts were observed (1.2 and 1.8 kb). Presumably these were transcribed from the additional nifH-homologous sequences present in the genome. These results are consistent with the existence of two N2 fixation systems in A. vinelandii which are regulated by molybdenum at the level of transcription.

摘要

在固氮菌维氏固氮菌中发现了多个与nifH同源的基因组区域。位于一个12.8千碱基(kb)XhoI片段上的nifHDK基因簇以及另外两个XhoI片段(7.4和8.4 kb)与nifH特异性DNA模板杂交,但7.4 kb和8.4 kb的片段未与nifD或nifK特异性DNA探针杂交。nifHDK基因簇的体内转录受氨抑制,且在去阻遏培养基中需要至少50 nM的钼存在。从nifHDK基因簇转录出三种mRNA,一种4.2 kb的转录本与nifH、nifD和nifK特异性DNA模板同源,一种2.6 kb的转录本与nifH和nifD特异性DNA模板同源,还有一种1.2 kb的转录本仅与nifH特异性DNA模板同源。在nifHDK缺失突变体CA11菌株中,未产生nifHDK特异性转录本,并且该菌株在存在浓度为50 nM或更高的Na2MoO4时无法在无氮培养基中生长。然而,在钼浓度为25 nM或更低时,在无氮培养基中出现生长。在这些条件下观察到两种与nifH同源(但与nifD或nifK不同源)的转录本(1.2和1.8 kb)。推测这些转录本是从基因组中存在的额外nifH同源序列转录而来的。这些结果与维氏固氮菌中存在两种受钼在转录水平调控的固氮系统一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/078e/212913/358cd32eaab0/jbacter00207-0062-a.jpg

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