Usuki Hirokazu, Nitoda Teruhiko, Ichikawa Misato, Yamaji Nahoko, Iwashita Takashi, Komura Hajime, Kanzaki Hiroshi
Laboratory of Bioresources Chemistry, The Graduate School of Natural Science and Technology, Okayama University, Okayama 700-8530, Japan.
J Am Chem Soc. 2008 Mar 26;130(12):4146-52. doi: 10.1021/ja077641f. Epub 2008 Feb 29.
A novel beta-N-acetylglucosaminidase (GlcNAcase) inhibitor named TMG-chitotriomycin (1) was isolated from the culture filtrate of Streptomyces anulatus NBRC13369. The strain produced 1 only when colloidal chitin was used as the sole carbon source in the production medium. The structure of 1 was determined by spectral and constitutive sugar analyses of the corresponding alditol derivatives to be an equilibrated mixture of alpha-d-N,N,N-triMeGlcNH2-(1,4)-beta-d-GlcNAc-(1,4)-beta-d-GlcNAc-(1,4)-d-GlcNAc and its C-2 epimer of the reducing end residue. TMG-chitotriomycin (1) showed potent and selective inhibition of insect and fungal GlcNAcases with no inhibition of mammalian and plant GlcNAcases. In contrast, the known GlcNAcase inhibitor nagstatin potently inhibited all GlcNAcases. It should be emphasized that synthesized d-N,N,N-triMeGlcNH2, which is the component sugar of 1, showed no inhibition of the insect Spodoptera litura GlcNAcase. These results suggest that the (GlcNAc)3 unit positioned at the reducing end of 1 is essential for its enzyme inhibitory activity. The unique inhibitory spectrum of 1 will be useful to study chitinolytic systems and to develop selective fungicides or pesticides.
一种名为TMG-壳三糖霉素(1)的新型β-N-乙酰氨基葡萄糖苷酶(GlcNAcase)抑制剂从环状链霉菌NBRC13369的培养滤液中分离得到。该菌株仅在生产培养基中使用胶体几丁质作为唯一碳源时才产生1。通过对相应糖醇衍生物的光谱和组成糖分析确定1的结构为α-d-N,N,N-三甲基葡糖胺-(1,4)-β-d- GlcNAc-(1,4)-β-d- GlcNAc-(1,4)-d- GlcNAc及其还原端残基的C-2差向异构体的平衡混合物。TMG-壳三糖霉素(1)对昆虫和真菌的GlcNAcase表现出强效且选择性的抑制作用,而对哺乳动物和植物的GlcNAcase没有抑制作用。相比之下,已知的GlcNAcase抑制剂纳他汀对所有GlcNAcase都有强效抑制作用。应该强调的是,合成的d-N,N,N-三甲基葡糖胺作为1的组成糖,对昆虫斜纹夜蛾的GlcNAcase没有抑制作用。这些结果表明,位于1还原端的(GlcNAc)3单元对其酶抑制活性至关重要。1独特的抑制谱将有助于研究几丁质分解系统以及开发选择性杀菌剂或杀虫剂。