Laboratory of Food Chemistry and Biochemistry & Leuven Food Science and Nutrition Research Centre, Katholieke Universiteit Leuven, Belgium.
Crit Rev Biotechnol. 2012 Jun;32(2):93-107. doi: 10.3109/07388551.2011.561537. Epub 2011 Jun 28.
Non-catalytic carbohydrate binding on independent carbohydrate-binding modules (CBMs) has been reported frequently for glycoside hydrolases (GHs) and reviewed thoroughly. However, various structural studies of GHs have revealed that non-catalytic carbohydrate binding sites can also occur on the surface of the structural unit comprising the active site. Here, the discovery of these sites, referred to as secondary binding sites (SBSs), and their putative roles in different GHs is reviewed for the first time. The majority of the SBSs have been discovered in starch-active enzymes, but there are also many reports of SBSs in various other enzymes. A wide variety of functions has been ascribed to these sites, including (1) targeting of the enzyme towards its substrate, (2) guiding the substrate into the active site groove, (3) substrate disruption, (4) enhancing processivity, (5) allosteric regulation, (6) passing on reaction products, and (7) anchoring to the cell wall of the parent microorganism. A lot of these putative functions are in agreement with the functions ascribed to non-catalytic binding in CBMs. Contrarily to CBMs, SBSs have a fixed position relative to the catalytic site, making them more or less suitable to take up specific functions.
非催化碳水化合物结合在独立的碳水化合物结合模块(CBMs)上已被频繁报道,并进行了深入研究。然而,各种糖苷水解酶(GHs)的结构研究表明,非催化碳水化合物结合位点也可能出现在包含活性位点的结构单元的表面上。本文首次综述了这些被称为次级结合位点(SBSs)的发现及其在不同 GHs 中的潜在作用。大多数 SBSs 已在淀粉活性酶中被发现,但也有许多关于各种其他酶中 SBSs 的报道。这些位点被赋予了广泛的功能,包括(1)将酶靶向其底物,(2)引导底物进入活性位点凹槽,(3)破坏底物,(4)提高进程性,(5)变构调节,(6)传递反应产物,以及(7)锚定到亲代微生物的细胞壁上。这些假定的功能中有很多与 CBMs 中归因于非催化结合的功能一致。与 CBMs 不同的是,SBSs 相对于催化位点具有固定的位置,这使得它们或多或少适合承担特定的功能。