Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, USA.
Appl Environ Microbiol. 2012 Sep;78(17):6194-202. doi: 10.1128/AEM.01312-12. Epub 2012 Jun 29.
Crenarchaeotal genomes encode the 3-hydroxypropionate/4-hydroxybutyrate (3-HP/4-HB) cycle for carbon dioxide fixation. Of the 13 enzymes putatively comprising the cycle, several of them, including methylmalonyl-coenzyme A (CoA) epimerase (MCE) and methylmalonyl-CoA mutase (MCM), which convert (S)-methylmalonyl-CoA to succinyl-CoA, have not been confirmed and characterized biochemically. In the genome of Metallosphaera sedula (optimal temperature [T(opt)], 73°C), the gene encoding MCE (Msed_0639) is adjacent to that encoding the catalytic subunit of MCM-α (Msed_0638), while the gene for the coenzyme B(12)-binding subunit of MCM (MCM-β) is located remotely (Msed_2055). The expression of all three genes was significantly upregulated under autotrophic compared to heterotrophic growth conditions, implying a role in CO(2) fixation. Recombinant forms of MCE and MCM were produced in Escherichia coli; soluble, active MCM was produced only if MCM-α and MCM-β were coexpressed. MCE is a homodimer and MCM is a heterotetramer (α(2)β(2)) with specific activities of 218 and 2.2 μmol/min/mg, respectively, at 75°C. The heterotetrameric MCM differs from the homo- or heterodimeric orthologs in other organisms. MCE was activated by divalent cations (Ni(2+), Co(2+), and Mg(2+)), and the predicted metal binding/active sites were identified through sequence alignments with less-thermophilic MCEs. The conserved coenzyme B(12)-binding motif (DXHXXG-SXL-GG) was identified in M. sedula MCM-β. The two enzymes together catalyzed the two-step conversion of (S)-methylmalonyl-CoA to succinyl-CoA, consistent with their proposed role in the 3-HP/4-HB cycle. Based on the highly conserved occurrence of single copies of MCE and MCM in Sulfolobaceae genomes, the M. sedula enzymes are likely to be representatives of these enzymes in the 3-HP/4-HB cycle in crenarchaeal thermoacidophiles.
泉古菌门的基因组编码了用于二氧化碳固定的 3-羟基丙酸/4-羟基丁酸(3-HP/4-HB)循环。在假定组成该循环的 13 种酶中,有几种酶,包括甲基丙二酰辅酶 A(CoA)差向异构酶(MCE)和甲基丙二酰辅酶 A 变位酶(MCM),它们将(S)-甲基丙二酰辅酶 A转化为琥珀酰辅酶 A,尚未得到生化确认和表征。在嗜热金属球菌(最适温度[T(opt)],73°C)的基因组中,编码 MCE(Msed_0639)的基因与编码 MCM-α的催化亚基(Msed_0638)相邻,而 MCM 的辅酶 B(12)结合亚基(MCM-β)的基因位于远程位置(Msed_2055)。与异养生长条件相比,所有这三个基因在自养生长条件下的表达均显著上调,表明它们在 CO(2)固定中发挥作用。在大肠杆菌中产生了重组形式的 MCE 和 MCM;仅当共表达 MCM-α和 MCM-β时,才能产生可溶性、活性的 MCM。MCE 是同源二聚体,MCM 是异四聚体(α(2)β(2)),在 75°C 时的比活性分别为 218 和 2.2 μmol/min/mg。与其他生物体中的同源或异源二聚体相比,异四聚体 MCM 有所不同。MCE 被二价阳离子(Ni(2+)、Co(2+)和 Mg(2+))激活,并且通过与较耐热 MCE 的序列比对确定了预测的金属结合/活性位点。在 M. sedula MCM-β 中鉴定到保守的辅酶 B(12)结合基序(DXHXXG-SXL-GG)。这两种酶一起催化(S)-甲基丙二酰辅酶 A 到琥珀酰辅酶 A 的两步转化,与它们在 3-HP/4-HB 循环中的预期作用一致。基于 Sulfolobaceae 基因组中单拷贝 MCE 和 MCM 的高度保守存在,M. sedula 酶很可能代表了古菌嗜热嗜酸菌 3-HP/4-HB 循环中的这些酶。