Useof Borate To Control the 5′-Position-Selective MicrobialGlucosylation ofPyridoxine

Author:

Wada Koichi1,Asano Yasuhisa1

Affiliation:

1. Biotechnology Research Center, Toyama Prefectural University, Kosugi, Toyama 939-0398, Japan

Abstract

ABSTRACT Nearly 100% 5′-position selectivity of transglucosylation from maltodextrin to pyridoxine (PN) by cells of Verticillium dahliae TPU 4900 was observed when the reaction was carried out with borate. The same effect of borate was observed not only during synthesis of pyridoxine 5′-α- d -glucoside by partially purified enzyme of this strain but also during synthesis of this compound by other microorganisms and with other enzymes (α-glucosidase and cyclomaltodextrin glucanotransferase). The effect was thought to be caused by the formation of a borate complex with 3- and 4′-position hydroxyl groups of PN. A decrease in the formation of pyridoxine 5′-α- d -glucoside was observed in the reaction with borate, but this decrease was overcome by optimizing the pH and increasing the amount of cells in the reaction mixture.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference29 articles.

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3. Böeseken, J. 1949. The use of boric acid for determination of the configuration of carbohydrate. Adv. Carbohydr. Chem.4:189-210.

4. Fujiwara Y. and T. Shinjutsu. October 1977. Japan patent 52128379.

5. Holmbarg, E., M. Holmquist, E. Hedenström, P. Berglund, T. Norin, H.-E. Högberg, and K. Hult. 1991. Reaction conditions for the resolution of 2-methylalkanoic acids in esterification and hydrolysis with lipase from Candida cylindracea. Appl. Microbiol. Biotechnol.35:572-578.

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