首页> 外文期刊>Carbohydrate research >Acinetobacter baumannii K13 and K73 capsular polysaccharides differ only in K-unit side branches of novel non-2-ulosonic acids: di- N-acetylated forms of either acinetaminic acid or 8-epiacinetaminic acid
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Acinetobacter baumannii K13 and K73 capsular polysaccharides differ only in K-unit side branches of novel non-2-ulosonic acids: di- N-acetylated forms of either acinetaminic acid or 8-epiacinetaminic acid

机译: b b菌(Baumannii) K13和K73荚膜多糖仅在新的非2余膦酸的K单元侧分支中不同:di- n - 乙酰化形式的少氨基酸或8-癫痫酰胺酸

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AbstractStructures of capsular polysaccharides ofAcinetobacter baumanniiisolates carrying KL13 and KL73 gene clusters were established. The closely related KL73 and KL13 gene clusters differ only by one gene in the module responsible for synthesis of the non-2-ulosonic acids. The K13 and K73 polysaccharides differ only in a single side-chain sugar, which is either 5,7-diacetamido-3,5,7,9-tetradeoxy-l-glycero-l-altro- or -d-glycero-l-altro-non-2-ulosonic acid [di-N-acetylated forms of acinetaminic acid (Aci5Ac7Ac) or 8-epiacinetaminic acid (8eAci5Ac7Ac), respectively].Display OmittedThe KL13 also is closely related to the KL12 gene cluster, which contains a differentwzygene encoding the K unit polymerase. Accordingly, the otherwise near identical K units are linked differently via an α-d-FucpNAc-(1?→?4)-d-Galplinkage in K13 and K73 or an α-d-FucpNAc-(1?→?3)-d-GalpNAc linkage in K12. This finding confirms the predicted substrate of the ItrB3 initiating transferase asd-FucpNAc. Glycosyltransferases predicted to catalyse the linkage of
机译:<![CDATA [ 抽象 斜视的胶囊多糖的结构:斜曲杆菌分离物携带KL13和KL73基因集群成立。密切相关的KL73和KL13基因簇仅在负责合成非2余膦酸的模块中的一个基因不同。 K13和K73多糖仅在单侧链糖中不同,这是5,7-二乙酰醇-3,5,7,9-四氧化 - L - 吉尔卡罗 - l - altro - 或 - d - 吉尔卡罗 - l - altro < / ce:斜体> - non-2-溃疡酸[分别的乙酰化形式的乙酰氨基酸(ACI5ac7ac)或8-eAiacetaminic酸(8Aci5ac7ac)]。 显示省略 KL13也与KL12基因集群密切相关,其中包含不同的 WZY 基因编码K单位聚合酶。因此,否则邻近相同的K单元通过α- d -fuc p nac-(1? →?4) - D -gal p K13和K73或α- D -FUC P NAC-(1?→?3) - D -gal p nac键在k12中。该发现证实了ITRB3启动转移酶的预测底物作为 D -FUC P NAC。糖基转移酶预测催化

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