Vu Van V, Marletta Michael A
NTT Hi-Tech Institute (NHTI), Nguyen Tat Thanh University, 298-300A Nguyen Tat Thanh Street, Ward 13, District 4, Ho Chi Minh City, Vietnam.
Department of Chemistry and Department of Molecular & Cell Biology, University of California, Berkeley, Berkeley, CA, 94720-3220, USA.
Cell Mol Life Sci. 2016 Jul;73(14):2809-19. doi: 10.1007/s00018-016-2251-9. Epub 2016 May 12.
Polysaccharide degradation by hydrolytic enzymes glycoside hydrolases (GHs) is well known. More recently, polysaccharide monooxygenases (PMOs, also known as lytic PMOs or LPMOs) were found to oxidatively degrade various polysaccharides via a copper-dependent hydroxylation. PMOs were previously thought to be either GHs or carbohydrate binding modules (CBMs), and have been re-classified in carbohydrate active enzymes (CAZY) database as auxiliary activity (AA) families. These enzymes include cellulose-active fungal PMOs (AA9, formerly GH61), chitin- and cellulose-active bacterial PMOs (AA10, formerly CBM33), and chitin-active fungal PMOs (AA11). These PMOs significantly boost the activity of GHs under industrially relevant conditions, and thus have great potential in the biomass-based biofuel industry. PMOs that act on starch are the latest PMOs discovered (AA13), which has expanded our perspectives in PMOs studies and starch degradation. Starch-active PMOs have many common structural features and biochemical properties of the PMO superfamily, yet differ from other PMO families in several important aspects. These differences likely correlate, at least in part, to the differences in primary and higher order structures of starch and cellulose, and chitin. In this review we will discuss the discovery, structural features, biochemical and biophysical properties, and possible biological functions of starch-active PMOs, as well as their potential application in the biofuel, food, and other starch-based industries. Important questions regarding various aspects of starch-active PMOs and possible economical driving force for their future studies will also be highlighted.
水解酶类糖苷水解酶(GHs)对多糖的降解作用已广为人知。最近,人们发现多糖单加氧酶(PMOs,也称为裂解性PMOs或LPMOs)可通过铜依赖性羟基化作用氧化降解各种多糖。PMOs以前被认为是GHs或碳水化合物结合模块(CBMs),并已在碳水化合物活性酶(CAZY)数据库中重新分类为辅助活性(AA)家族。这些酶包括纤维素活性真菌PMOs(AA9,以前为GH61)、几丁质和纤维素活性细菌PMOs(AA10,以前为CBM33)以及几丁质活性真菌PMOs(AA11)。这些PMOs在工业相关条件下能显著提高GHs的活性,因此在基于生物质的生物燃料行业具有巨大潜力。作用于淀粉的PMOs是最新发现的PMOs(AA13),这拓宽了我们对PMOs研究和淀粉降解的视野。淀粉活性PMOs具有PMO超家族的许多共同结构特征和生化特性,但在几个重要方面与其他PMO家族不同。这些差异可能至少部分与淀粉、纤维素和几丁质的一级和高级结构差异相关。在这篇综述中,我们将讨论淀粉活性PMOs的发现、结构特征、生化和生物物理特性以及可能的生物学功能,以及它们在生物燃料、食品和其他淀粉基行业中的潜在应用。还将强调关于淀粉活性PMOs各个方面的重要问题以及其未来研究可能的经济驱动力。