Wood H G
Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.
FASEB J. 1991 Feb;5(2):156-63. doi: 10.1096/fasebj.5.2.1900793.
An account is presented of the recent discovery of a pathway of growth by bacteria in which CO or CO2 and H2 are sources of carbon and energy. The Calvin cycle and subsequently other cycles were discovered in the 1950s, and in each the initial reaction of CO2 involved adding CO2 to an organic compound formed during the cyclic pathway (for example, CO2 and ribulose diphosphate). Studies were initiated in the 1950s with the thermophylic anaerobic organism Clostridium thermoaceticum, which Barker and Kamen had found fixed CO2 in both carbons of acetate during fermentation of glucose. The pathway of acetyl-CoA biosynthesis differs from all others in that two CO2 are combined with coenzyme A (CoASH) forming acetyl CoA, which then serves as the source of carbon for growth. This mechanism is designated the acetyl CoA pathway and some have called it the Wood pathway. A unique feature is the role of the enzyme carbon monoxide dehydrogenase (CODH), which catalyzes the conversion of CoASH, CO, and a methyl group to acetyl CoA, the final step of the pathway. The pathway involves the reduction of CO2 to formate, which then combines with tetrahydrofolate (THF) to form formyl THF. It in turn is reduced to CH3-THF. The methyl is then transferred to the cobalt on a corrinoid-containing enzyme. From there the methyl is transferred to CODH, and CO and CoASH bind with the enzyme at separate sites. Acetyl CoA is then synthesized. CODH would more properly be called carbon monoxide dehydrogenase-acetyl CoA synthase as it catalyzes oxidation of CO to CO2 and the synthesis of acetyl CoA. The solution of the mechanism of this pathway required more than 30 years, in part because the intermediate compounds are bound to enzymes, the enzymes are extremely sensitive to O2 and must be isolated under strictly anerobic conditions, and the role of a corrinoid and CODH was unprecedented. It is now apparent that this pathway occurs (perhaps with some modification) in many bacteria including the methane and sulfur bacteria. In some humans this pathway is catalyzed by the bacteria of the gut and acetate is produced rather than methane; it is calculated that 2.3 x 10(6) metric tons of acetate are formed daily from CO2. A similar synthesis occurs in the hind gut of termites. It is becoming apparent that the acetyl CoA pathway plays a significant role in the carbon cycle.(ABSTRACT TRUNCATED AT 400 WORDS)
本文介绍了细菌生长途径的最新发现,其中一氧化碳(CO)或二氧化碳(CO₂)与氢气是碳源和能源。卡尔文循环以及随后的其他循环在20世纪50年代被发现,在每个循环中,CO₂的初始反应是将CO₂添加到循环途径中形成的有机化合物上(例如,CO₂与二磷酸核酮糖)。20世纪50年代,人们开始对嗜热厌氧生物热醋梭菌进行研究,巴克和卡门发现该菌在葡萄糖发酵过程中能将CO₂固定在乙酸盐的两个碳原子中。乙酰辅酶A生物合成途径与其他所有途径不同,它是将两个CO₂与辅酶A(CoASH)结合形成乙酰辅酶A,然后乙酰辅酶A作为生长的碳源。这种机制被称为乙酰辅酶A途径,有些人称之为伍德途径。一个独特的特征是一氧化碳脱氢酶(CODH)的作用,它催化CoASH、CO和一个甲基转化为乙酰辅酶A,这是该途径的最后一步。该途径涉及将CO₂还原为甲酸,然后甲酸与四氢叶酸(THF)结合形成甲酰THF。甲酰THF又被还原为CH₃-THF。然后甲基转移到含类咕啉酶上的钴上。从那里甲基转移到CODH,CO和CoASH在不同位点与该酶结合。然后合成乙酰辅酶A。CODH更确切地应称为一氧化碳脱氢酶-乙酰辅酶A合酶,因为它催化CO氧化为CO₂并合成乙酰辅酶A。该途径机制的解析耗时30多年,部分原因是中间化合物与酶结合,这些酶对O₂极其敏感,必须在严格厌氧条件下分离,而且类咕啉和CODH的作用前所未闻。现在很明显,这条途径(可能有一些变体)存在于许多细菌中,包括甲烷菌和硫细菌。在一些人体内,这条途径由肠道细菌催化,产生的是乙酸盐而非甲烷;据计算,每天由CO₂形成2.3×10⁶公吨乙酸盐。类似的合成过程发生在白蚁的后肠中。越来越明显的是,乙酰辅酶A途径在碳循环中起着重要作用。(摘要截选至400字)