Isolation, identification, and characterization of pichia guilliermondii k123-1 and candida fermentati si, producing isoflavone β-glycosidase to hydrolyze isoflavone glycoside efficiently, from the korean traditional soybean paste

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Abstract

A total of 155 microbial strains were isolated from the Korean traditional soybean paste based on their morphological features on the growth of agar plate. Among the isolated strains, a total of 28 strains were capable of hydrolyzing isoflavone glycoside to isoflavone aglycone efficiently in the soybean paste. Finally, two strains, K123-1 and SI, were selected because of their resistance to 15% NaCl and ability to convert isoflavone glycoside to isoflavone aglycone efficiently during the fermentation of soybean paste. The isolated strains K123-1 and SI were identified to be Pichia guilli-ermondii and Candida fermentati, respectively, using the partial 26S rDNA sequence analysis and phylogenic analysis. Pichia guilliermondii K123-1 and Candida fermentati SI converted daidzin to daidzein up to 96% and 95%, respectively, and genistin to genistein up to 92% when soybean pastes were fermented at 30°C for 20 days with a single isolated strain. Pichia guilliermondii K123-1 and Candida fermentati SI were able to grow in the presence of 15% NaCl on both liquid medium and agar plate. We think that Pichia guilliermondii K123-1 and Candida fermentati SI might be one of good candidates for making functional soybean paste because they are isolated from the Korean traditional soybean paste and have a good ability to convert isoflavone glycosides to isoflavone aglycones and a high salt tolerance.

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Kim, W. C., So, J. H., Kim, S. I., Shin, J. H., Song, K. S., Yu, C. B., … Rhee, I. K. (2009). Isolation, identification, and characterization of pichia guilliermondii k123-1 and candida fermentati si, producing isoflavone β-glycosidase to hydrolyze isoflavone glycoside efficiently, from the korean traditional soybean paste. Journal of Applied Biological Chemistry, 52(4), 163–169. https://doi.org/10.3839/jabc.2009.028

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