Yu J P, Ladapo J, Whitman W B
Department of Microbiology, University of Georgia, Athens 30602-2605.
J Bacteriol. 1994 Jan;176(2):325-32. doi: 10.1128/jb.176.2.325-332.1994.
Methanococcus maripaludis, a facultatively autotrophic archaebacterium that grows with H2 or formate as the electron donor, does not assimilate sugars and other complex organic substrates. However, glycogen is biosynthesized intracellularly and commonly reaches values of 0.34% of the cellular dry weight in the early stationary phase. To determine the pathway of glycogen catabolism, specific enzymes of sugar metabolism were assayed in cell extracts. The following enzymes were found (specific activity in milliunits per milligram of protein): glycogen phosphorylase, 4.4; phosphoglucomutase, 10; glucose-6-phosphate isomerase, 9; 6-phosphofructokinase, 5.6, fructose-1,6-bisphosphatase, 10; fructose-1,6-bisphosphate aldolase, 4.2; triosephosphate isomerase, 44; glyceraldehyde-3-phosphate dehydrogenase, 26; phosphoglycerate kinase, 20; phosphoglycerate mutase, 78; enolase, 107; and pyruvate kinase, 4.0. Glyceraldehyde-3-phosphate dehydrogenase was NADP+ dependent, and the pyruvate kinase required MnCl2. The 6-phosphofructokinase had an unusually low pH optimum of 6.0. Four nonoxidative pentose-biosynthetic enzymes were found (specific activity in milliunits per milligram of protein): transketolase, 12; transaldolase, 24; ribulose-5-phosphate-3-epimerase, 55; and ribulose-5-phosphate isomerase, 100. However, the key enzymes of the oxidative pentose phosphate pathway, the reductive pentose phosphate pathway, and the classical and modified Entner-Duodoroff pathways were not detected. Thus, glycogen appears to be catabolized by the Embden-Meyerhoff-Parnas pathway. This result is in striking contrast to the nonmethanogenic archaebacteria that have been examined, among which the Entner-Doudoroff pathway is common. A dithiothreitol-specific NADP(+)-reducing activity was also found (8.5 mU/mg of protein). Other thiol compounds, such as cysteine hydrochloride, reduced glutathione, and 2-mercaptoethanesulfonic acid, did not replace dithiothreitol for this activity. The physiological significance of this activity is not known.
马氏甲烷球菌是一种兼性自养古细菌,以氢气或甲酸作为电子供体生长,不能同化糖类和其他复杂有机底物。然而,糖原在细胞内生物合成,在稳定期早期通常达到细胞干重的0.34%。为了确定糖原分解代谢途径,对细胞提取物中的糖代谢特定酶进行了测定。发现了以下酶(每毫克蛋白质的比活性,以毫单位计):糖原磷酸化酶,4.4;磷酸葡萄糖变位酶,10;葡萄糖-6-磷酸异构酶,9;6-磷酸果糖激酶,5.6;果糖-1,6-二磷酸酶,10;果糖-1,6-二磷酸醛缩酶,4.2;磷酸丙糖异构酶,44;甘油醛-3-磷酸脱氢酶,26;磷酸甘油酸激酶,20;磷酸甘油酸变位酶,78;烯醇化酶,107;丙酮酸激酶,4.0。甘油醛-3-磷酸脱氢酶依赖于NADP⁺,丙酮酸激酶需要MnCl₂。6-磷酸果糖激酶的最适pH值异常低,为6.0。发现了四种非氧化戊糖生物合成酶(每毫克蛋白质的比活性,以毫单位计):转酮醇酶,12;转醛醇酶,24;核糖ulose-5-磷酸-3-表异构酶,55;核糖ulose-5-磷酸异构酶,100。然而,未检测到氧化戊糖磷酸途径、还原戊糖磷酸途径以及经典和改良的恩特纳-杜德洛夫途径的关键酶。因此,糖原似乎通过糖酵解途径进行分解代谢。这一结果与已检测的非产甲烷古细菌形成鲜明对比,在这些非产甲烷古细菌中,恩特纳-杜德洛夫途径很常见。还发现了一种二硫苏糖醇特异性的NADP(⁺)还原活性(8.5毫单位/毫克蛋白质)。其他硫醇化合物,如盐酸半胱氨酸、还原型谷胱甘肽和2-巯基乙烷磺酸,不能替代二硫苏糖醇的这种活性。这种活性的生理意义尚不清楚。