Crystal Structure of Glucansucrase from the Dental Caries Pathogen Streptococcus mutans

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• 作者：Keisuke Ito¹ ; ^† ; ; Sohei Ito¹ ; ^† ; ; ^{itosohei@u-shizuoka-ken.ac.jp} ; Tatsuro Shimamura² ; ³ ; ^† ; ; Simone Weyand⁴ ; ⁵ ; Yasuaki Kawarasaki¹ ; Takumi Misaka⁶ ; Keiko Abe⁶ ; Takuya Kobayashi² ; ³ ; Alexander D. Cameron⁴ ; ⁵ ; So Iwata² ; ³ ; ⁴ ; ⁵
• 关键词：Streptococcus mutans ; glucansucrase ; dental caries ; glycoside hydrolase family 70 ; circularly permutation
• 刊名：Journal of Molecular Biology
• 出版年：2011
• 出版时间：29 April 2011
• 年：2011
• 卷：408
• 期：2
• 页码：177-186
• 全文大小：1497 K

文摘

Glucansucrase (GSase) from Streptococcus mutans is an essential agent in dental caries pathogenesis. Here, we report the crystal structure of S. mutans glycosyltransferase (GTF-SI), which synthesizes soluble and insoluble glucans and is a glycoside hydrolase (GH) family 70 GSase in the free enzyme form and in complex with acarbose and maltose. Resolution of the GTF-SI structure confirmed that the domain order of GTF-SI is circularly permuted as compared to that of GH family 13 α-amylases. As a result, domains A, B and IV of GTF-SI are each composed of two separate polypeptide chains. Structural comparison of GTF-SI and amylosucrase, which is closely related to GH family 13 amylases, indicated that the two enzymes share a similar transglycosylation mechanism via a glycosyl-enzyme intermediate in subsite − 1. On the other hand, novel structural features were revealed in subsites + 1 and + 2 of GTF-SI. Trp517 provided the platform for glycosyl acceptor binding, while Tyr430, Asn481 and Ser589, which are conserved in family 70 enzymes but not in family 13 enzymes, comprised subsite + 1. Based on the structure of GTF-SI and amino acid comparison of GTF-SI, GTF-I and GTF-S, Asp593 in GTF-SI appeared to be the most critical point for acceptor sugar orientation, influencing the transglycosylation specificity of GSases, that is, whether they produced insoluble glucan with α(1–3) glycosidic linkages or soluble glucan with α(1–6) linkages. The structural information derived from the current study should be extremely useful in the design of novel inhibitors that prevent the biofilm formation by GTF-SI.