Sugiyama Yasumasa, Nagasawa Hiromichi, Suzuki Akinori, Sakuda Shohei
Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Japan.
J Antibiot (Tokyo). 2002 Mar;55(3):263-9. doi: 10.7164/antibiotics.55.263.
Trehazolin (1) is a trehalase inhibitor produced by Micromonospora coriacea. Biosynthesis of 1 was studied by feeding experiments with a variety of labeled precursors. Feeding experiments with [1-13C]- and [6-13C]-D-glucose revealed that the carbon skeletons of both a glucose residue and a cyclopentane ring moiety in 1 were each derived from glucose, and that C-C bond formation between C-1 and C-5 of glucose occurred during the cyclopentane ring formation. Furthermore, an experiment with [guanidino-13C, 15N2]-L-arginine revealed that two nitrogen atoms and a quaternary carbon atom involved in the aminooxazoline moiety of 1 originated from an amidino group of arginine. Further feeding experiments with [1-2H]-, [2-2H]-, [4-2H]-, [6,6-2H2]- and [1,2,3,4,5,6,6-2H7]-D-glucose as well as [1-13C]-D-fructose showed that deuteriums on C-1, C-3, C-4 and C-6 of glucose were retained during the formation of the cyclopentane ring moiety of 1.
海藻糖酶抑制剂(1)是由坚韧小单孢菌产生的一种海藻糖酶抑制剂。通过用各种标记前体进行饲喂实验研究了1的生物合成。用[1-13C]-和[6-13C]-D-葡萄糖进行的饲喂实验表明,1中葡萄糖残基和环戊烷环部分的碳骨架均源自葡萄糖,并且在环戊烷环形成过程中葡萄糖的C-1和C-5之间发生了C-C键形成。此外,用[胍基-13C,15N2]-L-精氨酸进行的实验表明,1的氨基恶唑啉部分中涉及的两个氮原子和一个季碳原子源自精氨酸的脒基。用[1-2H]-、[2-2H]-、[4-2H]-、[6,6-2H2]-和[1,2,3,4,5,6,6-2H7]-D-葡萄糖以及[1-13C]-D-果糖进行的进一步饲喂实验表明,在1的环戊烷环部分形成过程中,葡萄糖C-1、C-3、C-4和C-6上的氘被保留。