Takahashi N, Sato T, Yamada T
Department of Oral Biochemistry, Tohoku University School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai, 980-8575, Japan.
J Bacteriol. 2000 Sep;182(17):4704-10. doi: 10.1128/JB.182.17.4704-4710.2000.
Metabolic pathways involved in the formation of cytotoxic end products by Porphyromonas gingivalis were studied. The washed cells of P. gingivalis ATCC 33277 utilized peptides but not single amino acids. Since glutamate and aspartate moieties in the peptides were consumed most intensively, a dipeptide of glutamate or aspartate was then tested as a metabolic substrate of P. gingivalis. P. gingivalis cells metabolized glutamylglutamate to butyrate, propionate, acetate, and ammonia, and they metabolized aspartylaspartate to butyrate, succinate, acetate, and ammonia. Based on the detection of metabolic enzymes in the cell extracts and stoichiometric calculations (carbon recovery and oxidation/reduction ratio) during dipeptide degradation, the following metabolic pathways were proposed. Incorporated glutamylglutamate and aspartylaspartate are hydrolyzed to glutamate and aspartate, respectively, by dipeptidase. Glutamate is deaminated and oxidized to succinyl-coenzyme A (CoA) by glutamate dehydrogenase and 2-oxoglutarate oxidoreductase. Aspartate is deaminated into fumarate by aspartate ammonia-lyase and then reduced to succinyl-CoA by fumarate reductase and acyl-CoA:acetate CoA-transferase or oxidized to acetyl-CoA by a sequential reaction of fumarase, malate dehydrogenase, oxaloacetate decarboxylase, and pyruvate oxidoreductase. The succinyl-CoA is reduced to butyryl-CoA by a series of enzymes, including succinate-semialdehyde dehydrogenase, 4-hydroxybutyrate dehydrogenase, and butyryl-CoA oxidoreductase. A part of succinyl-CoA could be converted to propionyl-CoA through the reactions initiated by methylmalonyl-CoA mutase. The butyryl- and propionyl-CoAs thus formed could then be converted into acetyl-CoA by acyl-CoA:acetate CoA-transferase with the formation of corresponding cytotoxic end products, butyrate and propionate. The formed acetyl-CoA could then be metabolized further to acetate.
研究了牙龈卟啉单胞菌形成细胞毒性终产物所涉及的代谢途径。牙龈卟啉单胞菌ATCC 33277的洗涤细胞利用肽但不利用单个氨基酸。由于肽中的谷氨酸和天冬氨酸部分消耗最为强烈,因此随后测试了谷氨酸或天冬氨酸的二肽作为牙龈卟啉单胞菌的代谢底物。牙龈卟啉单胞菌细胞将谷氨酰谷氨酸代谢为丁酸、丙酸、乙酸和氨,并且将天冬氨酰天冬氨酸代谢为丁酸、琥珀酸、乙酸和氨。基于在细胞提取物中对代谢酶的检测以及二肽降解过程中的化学计量计算(碳回收率和氧化/还原比),提出了以下代谢途径。掺入的谷氨酰谷氨酸和天冬氨酰天冬氨酸分别被二肽酶水解为谷氨酸和天冬氨酸。谷氨酸通过谷氨酸脱氢酶和2-氧代戊二酸氧化还原酶脱氨并氧化为琥珀酰辅酶A(CoA)。天冬氨酸通过天冬氨酸氨裂合酶脱氨为延胡索酸,然后通过延胡索酸还原酶和酰基辅酶A:乙酸辅酶A转移酶还原为琥珀酰辅酶A,或者通过延胡索酸酶、苹果酸脱氢酶、草酰乙酸脱羧酶和丙酮酸氧化还原酶的顺序反应氧化为乙酰辅酶A。琥珀酰辅酶A通过一系列酶,包括琥珀酸半醛脱氢酶、4-羟基丁酸脱氢酶和丁酰辅酶A氧化还原酶,还原为丁酰辅酶A。一部分琥珀酰辅酶A可以通过甲基丙二酰辅酶A变位酶引发的反应转化为丙酰辅酶A。由此形成的丁酰辅酶A和丙酰辅酶A然后可以通过酰基辅酶A:乙酸辅酶A转移酶转化为乙酰辅酶A,同时形成相应的细胞毒性终产物丁酸和丙酸。形成的乙酰辅酶A然后可以进一步代谢为乙酸。