Occurrence of Z-2-oxo-4-methyl-3-pentene-1,5-dioic acid and its regioisomer 4-methylene-2-oxo-glutaric acid in tulip tissues

Y. Kato, Taiji Nomura
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引用次数: 2

Abstract

Abstract Although Z-2-oxo-4-methyl-3-pentene-1,5-dioic acid (Z-OMPD) has been identified as a major dicarboxylic acid in tulip tissues, its biosynthetic pathway has not been elucidated. Herein, Z-OMPD was isolated from tulip leaves and chemically synthesized. Comparisons of these samples revealed that Z-OMPD exists as a tautomeric mixture at physiological pH. As a regioisomer of Z-OMPD, we enzymatically and chemically prepared 4-methylene-2-oxo-glutaric acid (4-MEOG) for the first time. Using these compounds as standards, the occurrence of Z-OMPD and 4-MEOG in various tissues of the tulip cultivar “Murasakizuisho” was evaluated directly and by 2,4-dinitrophenylhydrazone derivatization. Z-OMPD was found to be abundant in the aerial tissues, whereas 4-MEOG was almost absent from all tissues. Stability analyses of Z-OMPD and 4-MEOG revealed that no double bond isomerization occurred at physiological pH, suggesting that enzyme systems are responsible for Z-OMPD biosynthesis in tulip tissues.
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郁金香组织中z -2-氧-4-甲基-3-戊烯-1,5-二酸及其区域异构体4-亚甲基-2-氧-戊二酸的出现
摘要:虽然z -2-氧-4-甲基-3-戊烯-1,5-二酸(Z-OMPD)已被确定为郁金香组织中主要的二羧酸,但其生物合成途径尚未阐明。本文从郁金香叶片中分离并化学合成了Z-OMPD。结果表明,在生理ph下,Z-OMPD以互变异构体的形式存在。作为Z-OMPD的区域异构体,我们首次通过酶和化学方法制备了4-亚甲基-2-氧-戊二酸(4-MEOG)。以这些化合物为标准,用2,4-二硝基苯腙衍生化法直接测定了“Murasakizuisho”郁金香不同组织中Z-OMPD和4-MEOG的含量。发现Z-OMPD在空中组织中含量丰富,而4-MEOG在所有组织中几乎不存在。对Z-OMPD和4-MEOG的稳定性分析表明,在生理pH下,没有发生双键异构化,这表明酶系统在郁金香组织中负责Z-OMPD的生物合成。
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