Wood N J, Alizadeh T, Bennett S, Pearce J, Ferguson S J, Richardson D J, Moir J W
Department of Molecular Biology and Biotechnology, University of Sheffield, Sheffield S10 2TN, United Kingdom.
J Bacteriol. 2001 Jun;183(12):3606-13. doi: 10.1128/JB.183.12.3606-3613.2001.
Respiratory reduction of nitrate to nitrite is the first key step in the denitrification process that leads to nitrate loss from soils. In Paracoccus pantotrophus, the enzyme system that catalyzes this reaction is encoded by the narKGHJI gene cluster. Expression of this cluster is maximal under anaerobic conditions in the presence of nitrate. Upstream from narK is narR, a gene encoding a member of the FNR family of transcriptional activators. narR is transcribed divergently from the other nar genes. Mutational analysis reveals that NarR is required for maximal expression of the membrane-bound nitrate reductase genes and narK but has no other regulatory function related to denitrification. NarR is shown to require nitrate and/or nitrite is order to activate gene expression. The N-terminal region of the protein lacks the cysteine residues that are required for formation of an oxygen-sensitive iron-sulfur cluster in some other members of the FNR family. Also, NarR lacks a crucial residue involved in interactions of this family of regulators with the sigma(70) subunit of RNA polymerase, indicating that a different mechanism is used to promote transcription. narR is also found in Paracoccus denitrificans, indicating that this species contains at least three FNR homologues.
将硝酸盐还原为亚硝酸盐的呼吸作用是反硝化过程中的首个关键步骤,该过程会导致土壤中的硝酸盐流失。在嗜糖假单胞菌中,催化此反应的酶系统由narKGHJI基因簇编码。在厌氧条件下且存在硝酸盐时,该基因簇的表达量最高。narK上游是narR,它编码转录激活因子FNR家族的一个成员。narR与其他nar基因反向转录。突变分析表明,NarR是膜结合硝酸盐还原酶基因和narK最大表达所必需的,但与反硝化作用没有其他调控功能。已证明NarR需要硝酸盐和/或亚硝酸盐来激活基因表达。该蛋白质的N端区域缺少一些其他FNR家族成员形成对氧敏感的铁硫簇所需的半胱氨酸残基。此外,NarR缺少该调节因子家族与RNA聚合酶的σ(70)亚基相互作用所涉及的一个关键残基,这表明其采用了不同的机制来促进转录。在反硝化副球菌中也发现了narR,这表明该物种至少含有三个FNR同源物。