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In relation to this article, we declare that there is no conflict of interest.
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Received August 4, 2008
Accepted November 27, 2008
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Increased production of S-adenosyl-L-methionine using recombinant Saccharomyces cerevisiae sake K6

Department of Chemical & Bioengineering, Korea University, 5-1 Anam-dong, Sungbuk-gu, Seoul 136-713, Korea 1Samyang Genex, 63-2 Hwaam-dong, Yuseong-gu, Daejeon 305-717, Korea
mkoh@korea.ac.kr
Korean Journal of Chemical Engineering, January 2009, 26(1), 156-159(4), 10.1007/s11814-009-0025-x
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Abstract

S. cerevisiae sake K6 was the firstly isolated industrial strain to overproduce S-adenosyl-L-methionine (SAM). Although the strain has advantages over other strains, such as GRAS (generally recognized as safe) property, the S. cerevisiae K6 has not been further developed with DNA recombinant technology due to the lack of a proper genetic marker. In this study, UV mutagenesis was conducted with S. cerevisiae sake K6. With the method, a mutant of sake yeast with leucine auxotroph, K6-1, was isolated. The mutant showed comparable growth rate and SAM productivity with its wild type. Using the auxotroph as a genetic marker, a SAM synthase in S. cerevisiae, SAM2, was overexpressed in the mutant strain. This recombinant DNA technology successfully increased SAM productivity in sake yeast.

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