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光合细菌球形红杆菌DSM 158的周质硝酸盐还原系统:napKEFDABC基因簇的转录和突变分析

Periplasmic nitrate-reducing system of the phototrophic bacterium Rhodobacter sphaeroides DSM 158: transcriptional and mutational analysis of the napKEFDABC gene cluster.

作者信息

Reyes F, Gavira M, Castillo F, Moreno-Vivián C

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Córdoba, 14071-Córdoba, Spain.

出版信息

Biochem J. 1998 May 1;331 ( Pt 3)(Pt 3):897-904. doi: 10.1042/bj3310897.

Abstract

The phototrophic bacterium Rhodobacter sphaeroides DSM 158 is able to reduce nitrate to nitrite by means of a periplasmic nitrate reductase which is induced by nitrate and is not repressed by ammonium or oxygen. Recently, a 6.8 kb PstI DNA fragment carrying the napABC genes coding for this periplasmic nitrate-reducing system was cloned [Reyes, Roldán, Klipp, Castillo and Moreno-Vivián (1996) Mol. Microbiol. 19, 1307-1318]. Further sequence and genetic analyses of the DNA region upstream from the napABC genes reveal the presence of four additional nap genes. All these R. sphaeroides genes seem to be organized into a napKEFDABC transcriptional unit. In addition, a partial open reading frame similar to the Azorhizobium caulinodans yntC gene and the Escherichia coli yjcC and yhjK genes is present upstream from this nap gene cluster. The R. sphaeroides napK gene codes for a putative 6.3 kDa transmembrane protein which is not similar to known proteins and the napE gene codes for a 6.7 kDa transmembrane protein similar to the Thiosphaera pantotropha NapE. The R. sphaeroides napF gene product is a 16.4 kDa protein with four cysteine clusters that probably bind four [4Fe-4S] centres. This iron-sulphur protein shows similarity to the NapF and NapG proteins of E. coli and Haemophilus influenzae. Finally, the napD gene product is a 9.4 kDa soluble protein which is also found in E. coli and T. pantotropha. The 5' end of the nap transcript has been determined by primer extension, and a sigma70-like promoter has been identified upstream from the napK gene. The same transcriptional start site is found for cells growing aerobically or anaerobically with nitrate. Different mutant strains carrying defined polar and non-polar insertions in each nap gene were constructed. Characterization of these mutant strains demonstrates the participation of the nap gene products in the periplasmic nitrate reduction in R. sphaeroides.

摘要

光合细菌球形红杆菌DSM 158能够通过一种周质硝酸还原酶将硝酸盐还原为亚硝酸盐,该酶由硝酸盐诱导,不受铵或氧气抑制。最近,一个携带编码该周质硝酸还原系统的napABC基因的6.8 kb PstI DNA片段被克隆出来[雷耶斯、罗兰、克利普、卡斯蒂略和莫雷诺-维维安(1996年),《分子微生物学》,第19卷,第1307 - 1318页]。对napABC基因上游DNA区域的进一步序列和遗传分析揭示了另外四个nap基因的存在。球形红杆菌的所有这些基因似乎被组织成一个napKEFDABC转录单元。此外,在这个nap基因簇上游存在一个与茎瘤固氮根瘤菌yntC基因以及大肠杆菌yjcC和yhjK基因相似的部分开放阅读框。球形红杆菌napK基因编码一种推定的6.3 kDa跨膜蛋白,与已知蛋白不相似,而napE基因编码一种6.7 kDa跨膜蛋白,与泛养硫球菌NapE相似。球形红杆菌napF基因产物是一种16.4 kDa的蛋白,有四个半胱氨酸簇,可能结合四个[4Fe - 4S]中心。这种铁硫蛋白与大肠杆菌和流感嗜血杆菌的NapF和NapG蛋白相似。最后,napD基因产物是一种9.4 kDa的可溶性蛋白,也存在于大肠杆菌和泛养硫球菌中。通过引物延伸确定了nap转录本的5'端,并在napK基因上游鉴定出一个类似σ70的启动子。在有氧或无氧条件下以硝酸盐生长的细胞中发现了相同的转录起始位点。构建了在每个nap基因中携带特定极性和非极性插入的不同突变菌株。对这些突变菌株的表征证明了nap基因产物参与球形红杆菌周质中的硝酸盐还原。

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