Paul L, Ferguson D J, Krzycki J A
Department of Microbiology, Ohio State University, Columbus, Ohio.
J Bacteriol. 2000 May;182(9):2520-9. doi: 10.1128/JB.182.9.2520-2529.2000.
Three different methyltransferases initiate methanogenesis from trimethylamine (TMA), dimethylamine (DMA) or monomethylamine (MMA) by methylating different cognate corrinoid proteins that are subsequently used to methylate coenzyme M (CoM). Here, genes encoding the DMA and TMA methyltransferases are characterized for the first time. A single copy of mttB, the TMA methyltransferase gene, was cotranscribed with a copy of the DMA methyltransferase gene, mtbB1. However, two other nearly identical copies of mtbB1, designated mtbB2 and mtbB3, were also found in the genome. A 6.8-kb transcript was detected with probes to mttB and mtbB1, as well as to mtbC and mttC, encoding the cognate corrinoid proteins for DMA:CoM and TMA:CoM methyl transfer, respectively, and with probes to mttP, encoding a putative membrane protein which might function as a methylamine permease. These results indicate that these genes, found on the chromosome in the order mtbC, mttB, mttC, mttP, and mtbB1, form a single transcriptional unit. A transcriptional start site was detected 303 or 304 bp upstream of the translational start of mtbC. The MMA, DMA, and TMA methyltransferases are not homologs; however, like the MMA methyltransferase gene, the genes encoding the DMA and TMA methyltransferases each contain a single in-frame amber codon. Each of the three DMA methyltransferase gene copies from Methanosarcina barkeri contained an amber codon at the same position, followed by a downstream UAA or UGA codon. The C-terminal residues of DMA methyltransferase purified from TMA-grown cells matched the residues predicted for the gene products of mtbB1, mtbB2, or mtbB3 if termination occurred at the UAA or UGA codon rather than the in-frame amber codon. The mttB gene from Methanosarcina thermophila contained a UAG codon at the same position as the M. barkeri mttB gene. The UAG codon is also present in mttB transcripts. Thus, the genes encoding the three types of methyltransferases that initiate methanogenesis from methylamine contain in-frame amber codons that are suppressed during expression of the characterized methyltransferases.
三种不同的甲基转移酶通过甲基化不同的同源类咕啉蛋白启动三甲胺(TMA)、二甲胺(DMA)或甲胺(MMA)的甲烷生成,这些同源类咕啉蛋白随后用于甲基化辅酶M(CoM)。在此,首次对编码DMA和TMA甲基转移酶的基因进行了表征。TMA甲基转移酶基因mttB的单拷贝与DMA甲基转移酶基因mtbB1的一个拷贝共转录。然而,在基因组中还发现了另外两个几乎相同的mtbB1拷贝,分别命名为mtbB2和mtbB3。用针对mttB和mtbB1以及mtbC和mttC的探针检测到一个6.8 kb的转录本,mtbC和mttC分别编码DMA:CoM和TMA:CoM甲基转移的同源类咕啉蛋白,还用针对mttP的探针进行检测,mttP编码一种可能作为甲胺通透酶发挥作用的假定膜蛋白。这些结果表明,这些位于染色体上、顺序为mtbC、mttB、mttC、mttP和mtbB1的基因形成一个单一的转录单元。在mtbC翻译起始位点上游303或304 bp处检测到一个转录起始位点。MMA、DMA和TMA甲基转移酶并非同源物;然而,与MMA甲基转移酶基因一样,编码DMA和TMA甲基转移酶的基因各自都包含一个框内琥珀密码子。来自巴氏甲烷八叠球菌的三个DMA甲基转移酶基因拷贝在同一位置都含有一个琥珀密码子,后面跟着一个下游的UAA或UGA密码子。如果在UAA或UGA密码子而非框内琥珀密码子处发生终止,从TMA生长细胞中纯化的DMA甲基转移酶的C末端残基与mtbB1、mtbB2或mtbB3基因产物预测的残基相匹配。嗜热甲烷八叠球菌的mttB基因在与巴氏甲烷八叠球菌mttB基因相同的位置含有一个UAG密码子。UAG密码子也存在于mttB转录本中。因此,编码从甲胺启动甲烷生成的三种甲基转移酶的基因都含有框内琥珀密码子,这些密码子在已表征的甲基转移酶表达过程中被抑制。