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斯氏假单胞菌中反硝化作用的厌氧控制不受fnr样基因突变的影响。

Anaerobic control of denitrification in Pseudomonas stutzeri escapes mutagenesis of an fnr-like gene.

作者信息

Cuypers H, Zumft W G

机构信息

Lehrstuhl für Mikrobiologie, Universität Karlsruhe, Germany.

出版信息

J Bacteriol. 1993 Nov;175(22):7236-46. doi: 10.1128/jb.175.22.7236-7246.1993.

Abstract

The synthesis of proteins necessary for the respiratory reduction of nitrate to dinitrogen is induced in most denitrifying bacteria by a shift to anaerobiosis. A homolog of the fur gene, which encodes a redox-active transcriptional activator in Escherichia coli, was isolated from Pseudomonas stutzeri by using the anr gene of Pseudomonas aeruginosa as the hybridization probe (R. G. Sawers, Mol. Microbiol. 5:1469-1481, 1991). The coding region was located on a 3-kb SmaI fragment. An open reading frame of 735 nucleotides, designated fnrA, had the coding potential for a protein of 244 amino acids (M(r) = 27,089) with 51.2% positional identity to the Fnr protein of E. coli and 86.1% to the Anr protein of P. aeruginosa. The fnrA gene gave a single transcript of 0.85 kb and complemented nitrate-dependent anaerobic growth of an fnr deletion mutant of E. coli. An open reading frame immediately downstream of fnrA encoded adenine phosphoribosyltransferase (EC 2.4.2.7). Mutations in fnrA were generated in vitro by insertional mutagenesis followed by gene replacement. Gene inactivation was shown by loss of the fnrA transcript and detection of an arginine deiminase (EC 3.5.3.6)-negative phenotype in the mutants. However, neither the enzymatic activities nor the levels of anaerobic expression of the respiratory enzymes nitrate reductase (EC 1.7.99.4), nitrate reductase (EC 1.9.3.2), NO reductase (EC 1.7.99.7), and N2O reductase (EC 1.7.99.6) were changed in fnrA mutants versus the P. stutzeri wild type. A promoter-probe vector for Fnr-dependent transcription was activated anaerobically in the fnrA mutants, suggesting the existence of a second Fnr homolog in the same bacterium. The Fnr-binding motifs, apparent in the promoter region of genes encoding denitrification components of P. stutzeri, are likely to be recognized by this second Fnr homolog. Preliminary evidence indicates also the presence of the catabolite activator protein, Crp, in P. stutzeri.

摘要

在大多数反硝化细菌中,向厌氧环境的转变会诱导合成将硝酸盐呼吸还原为二氮所需的蛋白质。通过使用铜绿假单胞菌的anr基因作为杂交探针,从施氏假单胞菌中分离出了fur基因的一个同源物,该基因在大肠杆菌中编码一种具有氧化还原活性的转录激活因子(R.G.索尔斯,《分子微生物学》5:1469 - 1481,1991)。编码区位于一个3kb的SmaI片段上。一个735个核苷酸的开放阅读框,命名为fnrA,具有编码一个244个氨基酸蛋白质的潜力(分子量 = 27,089),与大肠杆菌的Fnr蛋白有51.2%的位置同一性,与铜绿假单胞菌的Anr蛋白有86.1%的位置同一性。fnrA基因产生一个0.85kb的单一转录本,并补充了大肠杆菌fnr缺失突变体的硝酸盐依赖性厌氧生长。fnrA下游紧邻的一个开放阅读框编码腺嘌呤磷酸核糖基转移酶(EC 2.4.2.7)。通过插入诱变随后进行基因替换,在体外产生了fnrA的突变。通过fnrA转录本的缺失以及在突变体中检测到精氨酸脱亚氨酶(EC 3.5.3.6)阴性表型,证明了基因失活。然而,与施氏假单胞菌野生型相比,fnrA突变体中呼吸酶硝酸盐还原酶(EC 1.7.99.4)、亚硝酸盐还原酶(EC 1.9.3.2)、一氧化氮还原酶(EC 1.7.99.7)和氧化亚氮还原酶(EC 1.7.99.6)的酶活性和厌氧表达水平均未改变。用于Fnr依赖性转录的启动子探针载体在fnrA突变体中被厌氧激活,这表明同一细菌中存在第二个Fnr同源物。施氏假单胞菌中编码反硝化成分的基因启动子区域中明显的Fnr结合基序,可能被这个第二个Fnr同源物识别。初步证据还表明施氏假单胞菌中存在分解代谢物激活蛋白Crp。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5940/206866/d48abad7b757/jbacter00064-0124-a.jpg

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