Kranz R G, Haselkorn R
Dept. of Molecular Genetics and Cell Biology, University of Chicago, IL 60637.
Gene. 1988 Nov 15;71(1):65-74. doi: 10.1016/0378-1119(88)90078-9.
Mutants of R. capsulatus that express nif genes constitutively with respect to ammonia were studied in order to define better the circuit that regulates nif gene transcription. One mutant class could be complemented in trans by a cosmid clone containing a wild-type gene (nifR5) defined by Tn5 inserts as being no longer than 1.6 kb. The nifR5 gene is unlinked to previously described nif genes. A second mutant class could not be complemented by the wild-type cosmid library. For one mutant in this class, a nifH::lac fusion was used to select further mutants that were Lac-. Only two of these could be complemented in trans to Lac+; the complementing gene was nifR4, which is analogous to the ntrA gene of enterobacteria. Both complemented strains were Nifc. Therefore these mutations do not bypass the need for the nifR4 gene product. A third class of constitutive mutant was found by selecting Nif+ revertants of a Nif- strain deleted for the nifR1 and nifR2 genes. The nifR1 and nifR2 genes are homologues of enterobacterial ntrC and ntrB genes, respectively. Not all of the Nif+ revertants were constitutive; some were regulated normally by ammonia. We suspect that the latter revertants use alternate Ntr systems to activate nif gene transcription, a suggestion consistent with the observation that numerous bands in Southern blots of total DNA of R. capsulatus are identified by Escherichia coli ntr gene probes.
为了更好地界定调节固氮基因转录的回路,对组成型表达固氮基因(相对于氨而言)的荚膜红细菌突变体进行了研究。一类突变体可以被一个包含野生型基因(nifR5)的黏粒克隆反式互补,该野生型基因由Tn5插入片段确定,长度不超过1.6 kb。nifR5基因与先前描述的固氮基因不连锁。另一类突变体不能被野生型黏粒文库互补。对于这类中的一个突变体,使用nifH::lac融合来筛选更多Lac-的突变体。其中只有两个可以被反式互补为Lac+;互补基因是nifR4,它类似于肠杆菌的ntrA基因。两个互补菌株都是Nifc。因此,这些突变并没有绕过对nifR4基因产物的需求。通过筛选缺失nifR1和nifR2基因的Nif-菌株的Nif+回复突变体,发现了第三类组成型突变体。nifR1和nifR2基因分别是肠杆菌ntrC和ntrB基因的同源物。并非所有的Nif+回复突变体都是组成型的;有些受氨的正常调节。我们怀疑后一类回复突变体使用替代的Ntr系统来激活固氮基因转录,这一推测与以下观察结果一致:荚膜红细菌总DNA的Southern印迹中的许多条带可被大肠杆菌ntr基因探针识别。