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对携带乌头酸异构酶的植物和昆虫相关细菌的检测与分子分析,该酶参与反式乌头酸生物合成,反式乌头酸是褐飞虱的拒食剂。

Detection and molecular analysis of plant- and insect-associated bacteria harboring aconitate isomerase involved in biosynthesis of trans-aconitic acid as antifeedant in brown planthoppers.

作者信息

Watanabe K, Katsuhara M, Nakao H, Sato M

机构信息

National Institute of Sericultural and Entomological Science, Tsukuba, Ibaraki 305, Japan.

出版信息

Curr Microbiol. 1997 Aug;35(2):97-102. doi: 10.1007/s002849900219.

Abstract

The activity of aconitate isomerase, which is involved in the biosynthesis of trans-aconitic acid as antifeedant in brown planthoppers, was detected in Pseudomonas fluorescens LRB3W1 and Pseudomonas putida MAFF301685 but not in Pseudomonas putida MAFF301684. The enzyme activity was induced in the presence of trans-aconitate, and therefore bacteria showing the enzyme activity were easily detected by their ability to grow on the minimal medium containing trans-aconitate as the sole carbon source (ACO agar medium). Experiments on growth of plant- or insect-associated bacteria on ACO agar medium showed that most of the Gram-negative bacteria displayed the aconitate isomerase activity unlike most of the Gram-positive bacteria isolated mainly from insects. Mini-Tn5 transposon derivatives of P. fluorescens LRB3W1 lacking completely or partially their ability to grow on ACO agar medium were obtained. Southern blot analysis with a mini-Tn5 DNA probe definitely showed that the genes responsible for the biosynthesis of aconitate isomerase present on chromosomal DNA. Thus, it was suggested that genes for aconitate isomerase biosynthesis are commonly present in Gram-negative plant- or insect-associated bacteria, and also the DNA fragments including the genes were detected in P. fluorescens LRB3W1.

摘要

乌头酸异构酶参与褐飞虱中作为拒食剂的反式乌头酸的生物合成,在荧光假单胞菌LRB3W1和恶臭假单胞菌MAFF301685中检测到了该酶的活性,但在恶臭假单胞菌MAFF301684中未检测到。该酶活性在反式乌头酸存在的情况下被诱导,因此,通过其在以反式乌头酸作为唯一碳源的基本培养基(ACO琼脂培养基)上生长的能力,可以很容易地检测到具有该酶活性的细菌。关于植物或昆虫相关细菌在ACO琼脂培养基上生长的实验表明,与主要从昆虫中分离出的大多数革兰氏阳性细菌不同,大多数革兰氏阴性细菌都具有乌头酸异构酶活性。获得了荧光假单胞菌LRB3W1完全或部分丧失在ACO琼脂培养基上生长能力的Mini-Tn5转座子衍生物。用Mini-Tn5 DNA探针进行的Southern印迹分析明确表明,负责乌头酸异构酶生物合成的基因存在于染色体DNA上。因此,有人提出,乌头酸异构酶生物合成基因通常存在于革兰氏阴性植物或昆虫相关细菌中,并且在荧光假单胞菌LRB3W1中也检测到了包含这些基因的DNA片段。

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