Miyamoto C M, Graham A F, Meighen E A
McGill University, Department of Biochemistry, Montreal, Quebec, Canada.
Nucleic Acids Res. 1988 Feb 25;16(4):1551-62. doi: 10.1093/nar/16.4.1551.
The nucleotide sequence of the luxC gene (1431 bp) and the upstream DNA (1049 bp) of the luminescent bacterium Vibrio harveyi has been determined. The luxC gene can be translated into a polypeptide of 55 kDa in excellent agreement with the molecular mass of the reductase polypeptide required for synthesis of the aldehyde substrate for the bioluminescent reaction. Analyses of codon usage showed a high frequency (1.9%) of the isoleucine codon, AUA, in the luxC gene compared to that found in Escherichia coli genes (0.2%) and its absence in the luxA, B and D genes. The low G/C content of the luxC gene and upstream DNA (38-39%) compared to that found in the other lux genes of V. harveyi (45%) was primarily due to a stretch of 500 nucleotides with only a 24% G/C content, extending from 200 bp inside lux C to 300 bp upstream. Moreover, an open reading frame did not extend for more than 48 codons between the luxC gene and 600 bp upstream at which point a gene transcribed in the opposite direction started. As the lux system in the luminescent bacterium, V. fischeri, contains a regulatory gene immediately upstream of luxC transcribed in the same direction, these results show that the organization and regulation of the lux genes have diverged in different luminescent bacteria.
哈维氏弧菌发光细菌的luxC基因(1431bp)及其上游DNA(1049bp)的核苷酸序列已被测定。luxC基因可被翻译成一个55kDa的多肽,这与生物发光反应醛底物合成所需还原酶多肽的分子量高度一致。密码子使用分析表明,与大肠杆菌基因(0.2%)相比,luxC基因中异亮氨酸密码子AUA的频率较高(1.9%),且在luxA、B和D基因中不存在该密码子。与哈维氏弧菌其他lux基因(45%)相比,luxC基因及其上游DNA的G/C含量较低(38 - 39%),这主要是由于一段500个核苷酸的序列,其G/C含量仅为24%,从luxC内部200bp延伸至上游300bp。此外,在luxC基因与上游600bp之间,开放阅读框延伸不超过48个密码子,在这一点上,一个反向转录的基因开始了。由于费氏弧菌发光细菌中的lux系统在luxC上游紧邻处含有一个同向转录的调控基因,这些结果表明lux基因的组织和调控在不同的发光细菌中已经发生了分化。