Nakajima Masahiro, Nishimoto Mamoru, Kitaoka Motomitsu
National Food Research Institute, National Agriculture and Food Research Organization., Kannondai, Tsukuba, Ibaraki, Japan.
Biosci Biotechnol Biochem. 2010;74(8):1652-5. doi: 10.1271/bbb.100263. Epub 2010 Aug 7.
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.
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。