Morii Hiroyuki, Koga Yosuke
Department of Chemistry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan.
J Bacteriol. 2003 Feb;185(4):1181-9. doi: 10.1128/JB.185.4.1181-1189.2003.
CDP-2,3-di-O-geranylgeranyl-sn-glycerol:L-serine O-archaetidyltransferase (archaetidylserine synthase) activity in cell extracts of Methanothermobacter thermautotrophicus cells was characterized. The enzyme catalyzed the formation of unsaturated archaetidylserine from CDP-unsaturated archaeol and L-serine. The identity of the reaction products was confirmed by thin-layer chromatography, fast atom bombardment-mass spectrum analysis, and chemical degradation. The enzyme showed maximal activity in the presence of 10 mM Mn2+ and 1% Triton X-100. Among various synthetic substrate analogs, both enantiomers of CDP-unsaturated archaeols with ether-linked geranylgeranyl chains and CDP-saturated archaeol with ether-linked phytanyl chains were similarly active toward the archaetidylserine synthase. The activity on the ester analog of the substrate was two to three times higher than that on the corresponding ether-type substrate. The activity of D-serine with the enzyme was 30% of that observed for L-serine. A trace amount of an acid-labile, unsaturated archaetidylserine intermediate was detected in the cells by a pulse-labeling experiment. A gene (MT1027) in M. thermautotrophicus genome annotated as the gene encoding phosphatidylserine synthase was found to be homologous to Bacillus subtilis pssA but not to Escherichia coli pssA. The substrate specificity of phosphatidylserine synthase from B. subtilis was quite similar to that observed for the M. thermautotrophicus archaetidylserine synthase, while the E. coli enzyme had a strong preference for CDP-1,2-diacyl-sn-glycerol. It was concluded that M. thermautotrophicus archaetidylserine synthase belongs to subclass II phosphatidylserine synthase (B. subtilis type) on the basis of not only homology but also substrate specificity and some enzymatic properties. The possibility that a gene encoding the subclass II phosphatidylserine synthase might be transferred from a bacterium to an ancestor of methanogens is discussed.
对嗜热自养甲烷杆菌细胞提取物中的CDP - 2,3 - 二 - O - 香叶基香叶基 - sn - 甘油:L - 丝氨酸O - 古菌磷脂酰转移酶(古菌磷脂酰丝氨酸合酶)活性进行了表征。该酶催化从CDP - 不饱和古菌醇和L - 丝氨酸形成不饱和古菌磷脂酰丝氨酸。通过薄层色谱、快原子轰击 - 质谱分析和化学降解确认了反应产物的身份。该酶在10 mM Mn2 + 和1% Triton X - 100存在下表现出最大活性。在各种合成底物类似物中,具有醚连接香叶基香叶基链的CDP - 不饱和古菌醇的两种对映体以及具有醚连接植烷链的CDP - 饱和古菌醇对古菌磷脂酰丝氨酸合酶的活性相似。底物酯类似物的活性比相应醚型底物的活性高两到三倍。D - 丝氨酸与该酶的活性是L - 丝氨酸观察活性的30%。通过脉冲标记实验在细胞中检测到微量的酸不稳定、不饱和古菌磷脂酰丝氨酸中间体。在嗜热自养甲烷杆菌基因组中注释为编码磷脂酰丝氨酸合酶的基因(MT1027)被发现与枯草芽孢杆菌pssA同源,但与大肠杆菌pssA不同源。枯草芽孢杆菌磷脂酰丝氨酸合酶的底物特异性与嗜热自养甲烷杆菌古菌磷脂酰丝氨酸合酶观察到的底物特异性非常相似,而大肠杆菌酶对CDP - 1,2 - 二酰基 - sn - 甘油有强烈偏好。基于同源性、底物特异性和一些酶学性质得出结论,嗜热自养甲烷杆菌古菌磷脂酰丝氨酸合酶属于II类磷脂酰丝氨酸合酶(枯草芽孢杆菌型)。讨论了编码II类磷脂酰丝氨酸合酶的基因可能从细菌转移到产甲烷菌祖先的可能性。