Baxter Nardia J, Hirt Robert P, Bodrossy Levente, Kovacs Kornel L, Embley T Martin, Prosser James I, Murrell J Colin
Department of Biological Sciences, University of Warwick, Coventry, CV4 7AL, UK.
Arch Microbiol. 2002 Apr;177(4):279-89. doi: 10.1007/s00203-001-0387-x. Epub 2002 Jan 31.
The genes encoding the ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) from Methylococcus capsulatus (Bath) were localised to an 8.3-kb EcoRI fragment of the genome. Genes encoding the large subunit ( cbbL), small subunit ( cbbS) and putative regulatory gene ( cbbQ) were shown to be located on one cluster. Surprisingly, cbbO, a second putative regulatory gene, was not located in the remaining 1.2-kb downstream (3') of cbbQ. However, probing of the M. capsulatus (Bath) genome with cbbO from Nitrosomonas europaea demonstrated that a cbbO homologue was contained within a separate 3.0-kb EcoRI fragment. Instead of a cbbR ORF being located upstream (5') of cbbL, there was a moxR-like ORF that was transcribed in the opposite direction to cbbL. There were three additional ORFs within the large 8.3-kb EcoRI fragment: a pyrE-like ORF, an rnr-like ORF and an incomplete ORF with no sequence similarity to any known protein. Phylogenetic analysis of cbbL from M. capsulatus (Bath) placed it within clade A of the green-type Form 1 Rubisco. cbbL was expressed in M. capsulatus (Bath) when grown with methane as a sole carbon and energy source under both copper-replete and copper-limited conditions. M. capsulatus (Bath) was capable of autotrophic growth on solid medium but not in liquid medium. Preliminarily investigations suggested that other methanotrophs may also be capable of autotrophic growth. Rubisco genes were also identified, by PCR, in Methylococcus-like strains and Methylocaldum species; however, no Rubisco genes were found in Methylomicrobium album BG8, Methylomonas methanica S1, Methylomonas rubra, Methylosinus trichosporium OB3b or Methylocystis parvus OBBP.
编码来自荚膜甲基球菌(巴斯)的核酮糖-1,5-二磷酸羧化酶/加氧酶(Rubisco)的基因定位于基因组的一个8.3 kb的EcoRI片段上。编码大亚基(cbbL)、小亚基(cbbS)和假定调控基因(cbbQ)的基因位于一个簇上。令人惊讶的是,第二个假定调控基因cbbO并不位于cbbQ下游(3')剩余的1.2 kb区域内。然而,用欧洲亚硝化单胞菌的cbbO对荚膜甲基球菌(巴斯)基因组进行探测表明,一个cbbO同源物包含在一个单独的3.0 kb EcoRI片段中。在cbbL的上游(5')并没有cbbR开放阅读框,而是有一个与cbbL转录方向相反的moxR样开放阅读框。在这个大的8.3 kb EcoRI片段内还有另外三个开放阅读框:一个pyrE样开放阅读框、一个rnr样开放阅读框和一个与任何已知蛋白质都没有序列相似性的不完整开放阅读框。对荚膜甲基球菌(巴斯)的cbbL进行系统发育分析,将其置于绿色型1型Rubisco的A进化枝内。当荚膜甲基球菌(巴斯)以甲烷作为唯一碳源和能源在铜充足和铜限制条件下生长时,cbbL都会表达。荚膜甲基球菌(巴斯)能够在固体培养基上自养生长,但在液体培养基中不能。初步研究表明,其他甲烷氧化菌可能也能够自养生长。通过PCR在类甲基球菌菌株和嗜甲基菌属物种中也鉴定到了Rubisco基因;然而,在白色甲基微菌BG8、甲烷甲基单胞菌S1、红色甲基单胞菌、嗜硫甲基孢囊菌OB3b或微小甲基囊菌OBBP中未发现Rubisco基因。