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利用磷酸化酶的联合作用实际制备D-半乳糖基-β1→4-L-鼠李糖。

Practical preparation of D-galactosyl-beta1-->4-L-rhamnose employing the combined action of phosphorylases.

作者信息

Nakajima Masahiro, Nishimoto Mamoru, Kitaoka Motomitsu

机构信息

National Food Research Institute, National Agriculture and Food Research Organization., Kannondai, Tsukuba, Ibaraki, Japan.

出版信息

Biosci Biotechnol Biochem. 2010;74(8):1652-5. doi: 10.1271/bbb.100263. Epub 2010 Aug 7.

Abstract

D-Galactosyl-beta1-->4-L-rhamnose (GalRha) was produced enzymatically from 1.1 M sucrose and 1.0 M L-rhamnose by the concomitant actions of four enzymes (sucrose phosphorylase, UDP-glucose-hexose 1-phosphate uridylyltransferase, UDP-glucose 4-epimerase, and D-galactosyl-beta1-->4-L-rhamnose phosphorylase) in the presence of 1.0 mM UDP-glucose and 30 mM inorganic phosphate. The accumulation of GalRha in 1 liter of the reaction mixture reached 230 g (the reaction yield was 71% from L-rhamnose). Sucrose and fructose in the reaction mixture were removed by yeast treatment, but isolation of GalRha by crystallization after yeast treatment was unsuccessful. Finally, 49 g of GalRha was isolated from part of the reaction mixture with yeast treatment by gel-filtration chromatography.

摘要

D-半乳糖基-β1→4-L-鼠李糖(GalRha)是在1.0 mM尿苷二磷酸葡萄糖(UDP-葡萄糖)和30 mM无机磷酸盐存在的情况下,通过四种酶(蔗糖磷酸化酶、UDP-葡萄糖-己糖1-磷酸尿苷酰转移酶、UDP-葡萄糖4-差向异构酶和D-半乳糖基-β1→4-L-鼠李糖磷酸化酶)协同作用,由1.1 M蔗糖和1.0 M L-鼠李糖酶促合成的。在1升反应混合物中,GalRha的积累量达到230克(以L-鼠李糖计反应产率为71%)。反应混合物中的蔗糖和果糖通过酵母处理去除,但酵母处理后通过结晶分离GalRha未成功。最后,通过凝胶过滤色谱法从部分经酵母处理的反应混合物中分离出49克GalRha。

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