In vitro biosynthesis of acetan using electroporated Acetobacter xylinum cells as enzyme preparations.

C E Semino, M A Dankert
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引用次数: 16

Abstract

Acetobacter xylinum strain NRRL B42 and its derivative RCGr1 produce a complex exopolysaccharide, acetan, containing glucose, mannose, glucuronic acid and rhamnose in a 4:1:1:1 molar ratio. The in vitro synthesis of acetan, employing electroporated cells as the enzyme system and the respective 14C-labelled sugar nucleotide precursors, is described. The synthesis of the prenyl-linked heptasaccharide repeat unit, already observed in EDTA-treated cells, was confirmed, as well as the formation of other saccharides not related to acetan biosynthesis, including a high molecular mass glucan. The acetan formed was characterized by gel filtration, specific radioactive labelling with each precursor and permethylation analysis. It was also shown that acetan contains acetyl residues and that using [14C]acetyl CoA as donor, radioactivity was detected both at the polysaccharide and at the prenyl-linked oligosaccharide stage.

以木醋杆菌细胞为酶制剂体外合成乙酰胺。
木醋杆菌(Acetobacter xylinum)菌株NRRL B42及其衍生物RCGr1以4:1:1:1的摩尔比生产含有葡萄糖、甘露糖、葡萄糖醛酸和鼠李糖的复合外多糖乙酰聚糖。乙酰的体外合成,采用电穿孔细胞作为酶系统和各自的14c标记的糖核苷酸前体,描述。已经在edta处理的细胞中观察到的戊烯基连接的七糖重复单元的合成得到了证实,以及其他与乙酰聚糖生物合成无关的糖类的形成,包括高分子量葡聚糖。形成的乙酰氨基被凝胶过滤,特异放射性标记与每个前体和过甲基化分析表征。研究还表明,乙酰聚糖含有乙酰基残基,以[14C]乙酰辅酶a为供体,在多糖和丙烯基连接的低聚糖阶段均检测到放射性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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