Pratte Brenda S, Thiel Teresa
Department of Biology, University of Missouri - St. Louis, Research 223, St. Louis, MO, 63121, USA.
Mol Microbiol. 2016 Jun;100(6):1096-109. doi: 10.1111/mmi.13370. Epub 2016 Apr 6.
The cyanobacterium Anabaena variabilis has two Mo-nitrogenases that function under different environmental conditions in different cell types. The heterocyst-specific nitrogenase encoded by the large nif1 gene cluster and the similar nif2 gene cluster that functions under anaerobic conditions in vegetative cells are under the control of the promoter for the first gene of each cluster, nifB1 or nifB2 respectively. Associated with each of these clusters is a putative regulatory gene called cnfR (patB) whose product has a C-terminal HTH domain and an N-terminal ferredoxin-like domain. CnfR1 activates nifB1 expression in heterocysts, while CnfR2 activates nifB2 expression. A cnfR1 mutant was unable to make nitrogenase under aerobic conditions in heterocysts while the cnfR2 mutant was unable to make nitrogenase under anaerobic conditions. Mutations in cnfR1 and cnfR2 reduced transcripts for the nif1 and nif2 genes respectively. The closely related cyanobacterium, Anabaena sp. PCC 7120 has the nif1 system but lacks nif2. Expression of nifB2:lacZ from A. variabilis in anaerobic vegetative cells of Anabaena sp. PCC 7120 depended on the presence of cnfR2. This suggests that CnfR2 is necessary and sufficient for activation of the nifB2 promoter and that the CnfR1/CnfR2 family of proteins are the primary activators of nitrogenase gene expression in cyanobacteria.
多变鱼腥蓝细菌有两种钼固氮酶,它们在不同环境条件下于不同细胞类型中发挥作用。由大的nif1基因簇编码的异形胞特异性固氮酶以及在营养细胞厌氧条件下起作用的相似nif2基因簇,分别受每个簇第一个基因nifB1或nifB2启动子的控制。与这些簇中的每一个相关联的是一个假定的调控基因,称为cnfR(patB),其产物具有C端螺旋-转角-螺旋结构域和N端铁氧化还原蛋白样结构域。CnfR1在异形胞中激活nifB1的表达,而CnfR2激活nifB2的表达。cnfR1突变体在有氧条件下的异形胞中无法产生固氮酶,而cnfR2突变体在厌氧条件下无法产生固氮酶。cnfR1和cnfR2中的突变分别减少了nif1和nif2基因的转录本。密切相关的蓝细菌鱼腥蓝细菌PCC 7120具有nif1系统但缺乏nif2。来自多变鱼腥蓝细菌的nifB2:lacZ在鱼腥蓝细菌PCC 7120的厌氧营养细胞中的表达取决于cnfR2的存在。这表明CnfR2对于激活nifB2启动子是必要且充分的,并且CnfR1/CnfR2蛋白家族是蓝细菌中固氮酶基因表达的主要激活因子。