Lloyd J S, De Marco P, Dalton H, Murrell J C
Department of Biological Sciences, University of Warwick, Coventry, CV4 7AL, UK.
Arch Microbiol. 1999 May-Jun;171(6):364-70. doi: 10.1007/s002030050723.
The methanotrophs Methylococcus capsulatus (Bath) and Methylosinus trichosporium OB3b contain particulate methane monooxygenase (pMMO) and soluble methane monooxygenase (sMMO) genes. Other methanotrophs such as Methylomicrobium album BG8 and Methylocystis parvus OBBP contain only pMMO genes. Although molecular genetic techniques are poorly developed in methanotrophs, sMMO genes were expressed in methanotrophs normally containing only pMMO genes. This was achieved by conjugation using broad-host-range plasmids containing the native promoter and sMMO genes from Mc. capsulatus (Bath) and Ms. trichosporium OB3b. sMMO genes derived from Ms. trichosporium OB3b were expressed in an active form in Mcy. parvus OBBP and in Mm. album BG8. Therefore, all of the genes required for active sMMO synthesis were contained on the broad-host-range plasmids and were expressed in the heterologous hosts. Constitutive synthesis of pMMO was observed in Mm. album BG8 when grown at high and low copper-to-biomass ratios, while transcription of the recombinant sMMO genes was only observed under growth conditions of low copper-to-biomass ratios. Therefore, the regulatory protein(s) for sMMO synthesis was also present on the plasmid used, or the heterologous host contained a regulatory system for sMMO. Expression of sMMO genes in methanotrophs containing only pMMO will assist further investigations on the expression and regulation of MMO genes in methanotrophs.
甲烷氧化菌荚膜甲基球菌(巴斯株)和 trichosporium OB3b 甲基弯曲菌含有颗粒性甲烷单加氧酶(pMMO)和可溶性甲烷单加氧酶(sMMO)基因。其他甲烷氧化菌,如 BG8 甲基微菌和微小甲基孢囊菌 OBBP 仅含有 pMMO 基因。尽管甲烷氧化菌中的分子遗传技术发展不完善,但 sMMO 基因在通常仅含有 pMMO 基因的甲烷氧化菌中得到了表达。这是通过使用含有来自荚膜甲基球菌(巴斯株)和 trichosporium OB3b 的天然启动子和 sMMO 基因的广宿主范围质粒进行接合来实现的。源自 trichosporium OB3b 的 sMMO 基因在微小甲基孢囊菌 OBBP 和 BG8 甲基微菌中以活性形式表达。因此,活性 sMMO 合成所需的所有基因都包含在广宿主范围质粒上,并在异源宿主中表达。当 BG8 甲基微菌在高铜与生物量比和低铜与生物量比下生长时,均观察到 pMMO 的组成型合成,而重组 sMMO 基因的转录仅在低铜与生物量比的生长条件下观察到。因此,用于 sMMO 合成的调节蛋白也存在于所使用的质粒上,或者异源宿主含有 sMMO 的调节系统。在仅含有 pMMO 的甲烷氧化菌中表达 sMMO 基因将有助于进一步研究甲烷氧化菌中 MMO 基因的表达和调控。