Jiang Ming, Cao Yang, Guo Zu-Feng, Chen Minjiao, Chen Xiaolei, Guo Zhihong
Department of Chemistry, Center for Cancer Research, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, China.
Biochemistry. 2007 Sep 25;46(38):10979-89. doi: 10.1021/bi700810x. Epub 2007 Aug 31.
Menaquinone is an electron carrier in the respiratory chain of Escherichia coli during anaerobic growth. Its biosynthesis involves (1R,6R)-2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylic acid (SHCHC) as an intermediate, which is believed to be derived from isochorismate and 2-ketoglutarate by one of the biosynthetic enzymes-MenD. However, we found that the genuine MenD product is 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic acid (SEPHCHC), rather than SHCHC. This is supported by the following findings: (i) isochorismate consumption and SHCHC formation are not synchronized in the enzymic reaction, (ii) the rate of SHCHC formation is independent of the enzyme concentration, (iii) SHCHC is not formed in weakly acidic or neutral solutions in which the isochorismate substrate is readily consumed by MenD, and (iv) the MenD turnover product, formed under conditions disabling SHCHC formation, possesses spectroscopic characteristics consistent with the structure of SEPHCHC and spontaneously undergoes 2,5-elimination to form SHCHC and pyruvate in weakly basic solutions. Two properties of the intermediate, ultraviolet transparency and chemical instability, provide a rationale for the fact that SHCHC has been consistently mistaken as the MenD product. In accordance with these findings, MenD was rediscovered to be a highly efficient enzyme with a high second-order rate constant and should be renamed SEPHCHC synthase. Intriguingly, the enzymatic activity responsible for conversion of SEPHCHC into SHCHC appears not to associate with any of the known enzymes in menaquinone biosynthesis but is present in the crude extract of E. coli K12, suggesting that a genuine SHCHC synthase remains to be identified to fully elucidate the ubiquitous biosynthetic pathway.
甲萘醌是大肠杆菌在厌氧生长过程中呼吸链中的一种电子载体。其生物合成涉及(1R,6R)-2-琥珀酰-6-羟基-2,4-环己二烯-1-羧酸(SHCHC)作为中间体,据信它是由生物合成酶MenD从异分支酸和2-酮戊二酸衍生而来。然而,我们发现真正的MenD产物是2-琥珀酰-5-烯醇丙酮酸-6-羟基-3-环己烯-1-羧酸(SEPHCHC),而非SHCHC。以下发现支持了这一点:(i)在酶促反应中,异分支酸的消耗和SHCHC的形成不同步;(ii)SHCHC的形成速率与酶浓度无关;(iii)在弱酸性或中性溶液中不形成SHCHC,而异分支酸底物在这些溶液中很容易被MenD消耗;(iv)在使SHCHC形成受阻的条件下形成的MenD周转产物具有与SEPHCHC结构一致的光谱特征,并且在弱碱性溶液中会自发进行2,5-消除反应形成SHCHC和丙酮酸。中间体的两个特性,即紫外线透明性和化学不稳定性,解释了为何SHCHC一直被错误地认为是MenD产物。根据这些发现,MenD被重新发现是一种具有高二级速率常数的高效酶,应重新命名为SEPHCHC合酶。有趣的是,负责将SEPHCHC转化为SHCHC的酶活性似乎与甲萘醌生物合成中任何已知的酶都不相关,但存在于大肠杆菌K12的粗提物中,这表明仍有待鉴定一种真正的SHCHC合酶,以全面阐明这一普遍存在的生物合成途径。