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台湾乳白蚁β-葡萄糖苷酶体内抑制剂的筛选方法

Screening method for inhibitors against formosan subterranean termite beta-glucosidases in vivo.

作者信息

Zhu Betty C R, Henderson Gregg, Laine Roger A

机构信息

Department of Entomology, Louisiana State University Agricultural Center, Louisiana Agricultural Experimental Station, Baton Rouge, LA 70803, USA.

出版信息

J Econ Entomol. 2005 Feb;98(1):41-6. doi: 10.1093/jee/98.1.41.

Abstract

Cellulose, a main structural constituent of plants, is the major nutritional component for wood-feeding termites. Enzymatic hydrolysis of cellulose to glucose occurs by the action of cellulases, a mixture of the three major classes of enzymes including endo-1,4-beta-glucanases, exo-1,4-beta-glucanases, and beta-glucosidase. Lower termites, such as the Formosan subterranean termite, Coptotermes formosanus Shiraki, require cellulolytic protozoa to efficiently digest cellulose for survival. Inhibitors developed against any of these cellulase system enzymes would be a potential termite treatment avenue. Our effort was to develop a screening system to determine whether termites could be controlled by administration of cellulase system inhibitors. Some reported compounds such as gluconolactone, conduritol B epoxide, and 1-deoxynojirimycin are potential beta-glucosidase inhibitors, but they have only been tested in vitro. We describe an in vivo method to test the inhibitory ability of the designated chemicals to act on beta-1,4-glucosidases, one member of the cellulase system that is the key step that releases glucose for use as an energy and carbon source for termites. Inhibition in releasing glucose from cellooligosaccharides might be sufficient to starve termites. Fluorescein di-beta-D-glucopyranoside was used as the artificial enzyme substrate and the fluorescent intensity of the reaction product (fluorescein) quantified with an automated fluorescence plate reader. Several known in vitro beta-1,4-glucosidase inhibitors were tested in vivo, and their inhibitory potential was determined. Endogenous and protozoan cellulase activities are both assumed to play a role.

摘要

纤维素是植物的主要结构成分,是食木白蚁的主要营养成分。纤维素在纤维素酶的作用下被酶解为葡萄糖,纤维素酶是包括内切-1,4-β-葡聚糖酶、外切-1,4-β-葡聚糖酶和β-葡萄糖苷酶这三大类酶的混合物。较低等的白蚁,如台湾乳白蚁(Coptotermes formosanus Shiraki),需要纤维素分解原生动物来有效消化纤维素以维持生存。针对这些纤维素酶系统中的任何一种酶开发的抑制剂都将是一种潜在的白蚁防治途径。我们的工作是开发一种筛选系统,以确定是否可以通过施用纤维素酶系统抑制剂来控制白蚁。一些报道的化合物,如葡萄糖酸内酯、conduritol B环氧化物和1-脱氧野尻霉素,是潜在的β-葡萄糖苷酶抑制剂,但它们仅在体外进行了测试。我们描述了一种体内方法,用于测试指定化学物质对β-1,4-葡萄糖苷酶(纤维素酶系统的一个成员,是释放葡萄糖以供白蚁用作能量和碳源的关键步骤)的抑制能力。抑制从纤维寡糖释放葡萄糖可能足以使白蚁饥饿。荧光素二-β-D-吡喃葡萄糖苷被用作人工酶底物,反应产物(荧光素)的荧光强度用自动荧光酶标仪进行定量。几种已知的体外β-1,4-葡萄糖苷酶抑制剂在体内进行了测试,并确定了它们的抑制潜力。内源性和原生动物纤维素酶活性都被认为起作用。

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