Schwacha A, Bender R A
Department of Biology, University of Michigan, Ann Arbor 48109-1048.
J Bacteriol. 1993 Apr;175(7):2107-15. doi: 10.1128/jb.175.7.2107-2115.1993.
The Klebsiella aerogenes nac gene, whose product is necessary for nitrogen regulation of a number of operons, was identified and its DNA sequence determined. The nac sequence predicted a protein a 305 amino acids with a strong similarity to members of the LysR family of regulatory proteins, especially OxyR from Escherichia coli. Analysis of proteins expressed in minicells showed that nac is a single-gene operon whose product has an apparent molecular weight of about 32 kDa as measured in sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Immediately downstream from nac is a two-gene operon, the first gene of which encodes another member of the LysR family. Upstream from nac is a tRNAAsn gene transcribed divergently from nac. About 60 bp upstream from the nac open reading frame lies a sequence nearly identical to the consensus for sigma 54-dependent promoters, with the conserved GG and GC nucleotides at -26 and -14 relative to the start of transcription. About 130 bp farther upstream (at -153 relative to the start of transcription) is a sequence nearly identical to the transcriptional activator NTRC-responsive enhancer consensus. Another weaker NTRC-binding site is located adjacent to this site (at -133 relative to the start of transcription). Thus, we propose that nac is transcribed by RNA polymerase carrying sigma 54 in response to the nitrogen regulatory (NTR) system. A transposon located between the promoter and the nac ORF prevented NTR-mediated expression of nac, supporting this identification of the promoter sequence. The insertion of over 5 kb of transposon DNA between the enhancer and its target promoter had only a weak effect on enhancer-mediated regulation, suggesting that enhancers may be able to act at a considerable distance on the bacterial chromosome.
产气克雷伯菌的nac基因被鉴定出来,其产物对于许多操纵子的氮调节是必需的,并测定了其DNA序列。nac序列预测的蛋白质有305个氨基酸,与调节蛋白LysR家族成员,特别是大肠杆菌的OxyR有很强的相似性。在小细胞中表达的蛋白质分析表明,nac是一个单基因操纵子,其产物在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳中测得的表观分子量约为32 kDa。nac的紧下游是一个双基因操纵子,其第一个基因编码LysR家族的另一个成员。nac的上游是一个从nac反向转录的tRNAAsn基因。在nac开放阅读框上游约60 bp处有一个与σ54依赖型启动子的共有序列几乎相同的序列,相对于转录起始点,在-26和-14处有保守的GG和GC核苷酸。在更远的上游约130 bp处(相对于转录起始点为-153)有一个与转录激活因子NTRC反应增强子共有序列几乎相同的序列。另一个较弱的NTRC结合位点位于该位点附近(相对于转录起始点为-133)。因此,我们提出nac由携带σ54的RNA聚合酶响应氮调节(NTR)系统进行转录。位于启动子和nac开放阅读框之间的转座子阻止了NTR介导的nac表达,支持了对启动子序列的这种鉴定。在增强子与其靶启动子之间插入超过5 kb的转座子DNA对增强子介导的调节只有微弱的影响,这表明增强子可能能够在细菌染色体上相当远的距离起作用。