Karunakaran T, Madden T, Kuramitsu H
Department of Oral Biology, State University of New York at Buffalo 14214-3092, USA.
J Bacteriol. 1997 Mar;179(6):1898-908. doi: 10.1128/jb.179.6.1898-1908.1997.
An hemR (hemin-regulated) gene from Porphyromonas gingivalis ATCC 53977 has been isolated and characterized. This gene is present downstream from the prtT gene, previously cloned in this laboratory. In addition, another putative gene, ORF1, was identified between hemR and prtT. The complete nucleotide sequences of ORF1 and hemR were determined, and the deduced amino acid sequence of ORF1 and HemR proteins corresponded to 16- and 48-kDa proteins, respectively. The amino termini of the HemR protein exhibited significant homology with iron-regulated, TonB-dependent outer membrane receptor proteins from various bacteria, while the carboxyl terminus of the HemR protein displayed almost complete identity with a P. gingivalis PrtT protease domain. PCR analyses confirmed the existence of such extensive homology between the carboxyl termini of both the prtT and hemR genes on the P. gingivalis chromosome. Northern blots indicated that ORF1 was part of a 1.0-kb mRNA and was positively regulated by hemin levels. On the other hand, the hemR gene was apparently a part of a 3.0-kb polycistronic message and was negatively regulated at the transcriptional level by hemin. Primer extension analysis of the hemR gene revealed that the transcription start site was at a C residue located within ORF1. An examination of HemR::lacZ constructs in both Escherichia coli and P. gingivalis confirmed hemin repression of hemR expression in both organisms. Moreover, the HemR protein expressed in E. coli was detected by an antiserum from a periodontitis patient heavily colonized with P. gingivalis but not by serum from a periodontally healthy patient or by antisera against hemin-grown P. gingivalis cells. Therefore, it is likely that the 48-kDa HemR protein can be expressed only under hemin-restricted conditions. These results suggest that we have isolated a hemin-regulated gene, hemR, which encodes a 48-kDa protein that may be a TonB-dependent outer membrane protein.
已从牙龈卟啉单胞菌ATCC 53977中分离并鉴定出一个hemR(血红素调节)基因。该基因位于先前在本实验室克隆的prtT基因下游。此外,在hemR和prtT之间鉴定出另一个假定基因ORF1。确定了ORF1和hemR的完整核苷酸序列,推导的ORF1和HemR蛋白的氨基酸序列分别对应于16 kDa和48 kDa的蛋白。HemR蛋白的氨基末端与来自各种细菌的铁调节、TonB依赖性外膜受体蛋白具有显著同源性,而HemR蛋白的羧基末端与牙龈卟啉单胞菌PrtT蛋白酶结构域几乎完全相同。PCR分析证实牙龈卟啉单胞菌染色体上prtT和hemR基因的羧基末端之间存在如此广泛的同源性。Northern印迹表明ORF1是1.0 kb mRNA的一部分,并受血红素水平的正向调节。另一方面,hemR基因显然是3.0 kb多顺反子信息的一部分,并在转录水平受血红素的负向调节。对hemR基因的引物延伸分析表明转录起始位点位于ORF1内的一个C残基处。对大肠杆菌和牙龈卟啉单胞菌中HemR::lacZ构建体的检测证实了两种生物体中hemR表达均受血红素抑制。此外,用来自牙龈卟啉单胞菌大量定植的牙周炎患者的抗血清检测到了在大肠杆菌中表达的HemR蛋白,但未被牙周健康患者的血清或针对血红素培养的牙龈卟啉单胞菌细胞的抗血清检测到。因此,48 kDa的HemR蛋白可能仅在血红素受限的条件下表达。这些结果表明我们分离出了一个血红素调节基因hemR,它编码一种48 kDa蛋白,可能是一种TonB依赖性外膜蛋白。