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Evolutionary engineering of Phaffia rhodozyma for astaxanthin-overproducing strain 被引量:1

Evolutionary engineering of Phaffia rhodozyma for astaxanthin-overproducing strain
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摘要 Evolutionary engineering is a novel whole- genome wide engineering strategy inspired by natural evolution for strain improvement. Astaxanthin has been widely used in cosmetics, pharmaceutical and health care food due to its capability of quenching active oxygen. Strain improvement ofPhaffia rhodozyma, one of the main sources for natural astaxanthin, is of commercial interest for astaxanthin production. In this study a selection procedure was developed for adaptive evolution of P. rhodozyma strains under endogenetic selective pressure induced by additive in environmental niches. Six agents, which can induce active oxygen in cells, were added to the culture medium respectively to produce selective pressure in process of evolution. The initial strain, P. rhodozyma AS2-1557, was mutagenized to acquire the initial strain population, which was then cultivated for 550 h at selective pressure and the culture was transferred every 48h. Finally, six evolved strains were selected after 150 generations of evolution. The evolved strains produced up to 48.2% more astaxanthin than the initial strain. Our procedure may provide a promising alternative for improvement of highproduction strain. Evolutionary engineering is a novel whole- genome wide engineering strategy inspired by natural evolution for strain improvement. Astaxanthin has been widely used in cosmetics, pharmaceutical and health care food due to its capability of quenching active oxygen. Strain improvement ofPhaffia rhodozyma, one of the main sources for natural astaxanthin, is of commercial interest for astaxanthin production. In this study a selection procedure was developed for adaptive evolution of P. rhodozyma strains under endogenetic selective pressure induced by additive in environmental niches. Six agents, which can induce active oxygen in cells, were added to the culture medium respectively to produce selective pressure in process of evolution. The initial strain, P. rhodozyma AS2-1557, was mutagenized to acquire the initial strain population, which was then cultivated for 550 h at selective pressure and the culture was transferred every 48h. Finally, six evolved strains were selected after 150 generations of evolution. The evolved strains produced up to 48.2% more astaxanthin than the initial strain. Our procedure may provide a promising alternative for improvement of highproduction strain.
出处 《Frontiers of Chemical Science and Engineering》 CAS CSCD 2012年第2期174-178,共5页 化学科学与工程前沿(英文版)
基金 Acknowledgements This work was supported by the National Basic Research Program of China (973) (Grant No. 2007CB707802), and the National Natural Science Foundation of China (Grant Nos. 20806055, 20875068).
关键词 evolutionary engineering ASTAXANTHIN strain improvement evolutionary engineering, astaxanthin, strain improvement
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  • 1Selifonova O,Valle F,Schellenberger V. Rapid evolution of novel traits in microorganisms[J].Applied and Environmental Microbiology,2001,(08):3645-3649.doi:10.1128/AEM.67.8.3645-3649.2001.
  • 2Sonderegger M,Sauer U. Evolutionary engineering of Saccharomyces cerevisiae for anaerobic growth on xylose[J].Applied and Environmental Microbiology,2003,(04):1990-1998.doi:10.1016/j.jocn.2009.06.010.
  • 3Steiner P,Sauer U. Long-term continuous evolution of acetate resistant Acetobacter aceti[J].Biotechnology and Bioengineering,2003,(01):40-44.doi:10.1002/bit.10741.
  • 4van Maris A J A,Geertman J M A,Vermeulen A,Grroothuizen M K Winkler A A Piper M D W van Dijken J P Pronk J T. Directed evolution of pyruvate decarboxylase-negative Saccharomyces cerevisiae,yielding a C-2-independent,glucose-tolerant,and pyruvate-hyperproducing yeast[J].Applied and Environmental Microbiology,2004,(01):159-166.doi:10.1128/AEM.70.1.159-166.2004.
  • 5Cakar Z P,Seker U O S,Tamerler C,Sonderegger M Sauer U. Evolutionary engineering of multiple-stress resistant Saccharomyces cerevisiae[J].FEMS Yeast Research,2005,(6-7):569-578.doi:10.1016/j.femsyr.2004.10.010.
  • 6Kuyper M,Toirkens M,Diderich J,Winkler A Vandijken J Pronk J. Evolutionary engineering of mixed-sugar utilization by a xylosefermenting Saccharomyces cerevisiae strain[J].FEMS Yeast Research,2005.925-934.doi:10.1159/000334055.
  • 7Wisselink H W,Toirkens M J,del Rosario Franco Berriel M,Winkler A A van Dijken J P Pronk J T van Maris A J A. Engineering of Saccharomyces cerevisiae for efficient anaerobic alcoholic fermentation of L-arabinose[J].Applied and Environmental Microbiology,2007,(15):4881-4891.doi:10.1128/AEM.00177-07.
  • 8Guimaraes P M R,Francois J,Parrou J L,Teixeira J A Domingues L. Adaptive evolution of a lactose-consuming Saccharomyces cerevisiae recombinant[J].Applied and Environmental Microbiology,2008,(06):1748-1756.doi:10.1128/AEM.00186-08.
  • 9Jantama K,Haupt M J,Svoronos S A,Zhang X Moore J C Shanmugam K T Ingram L O. Combining metabolic engineering and metabolic evolution to develop nonrecombinant strains of Escherichia coli C that produce succinate and malate[J].Biotechnology and Bioengineering,2008,(05):1140-1153.doi:10.1002/bit.21694.
  • 10Meijnen J P,de Winde J H,Ruijssenaars H J. Engineering pseudomonas putida S 12 for efficient utilization of D-xylose and Larabinose[J].Applied and Environmental Microbiology,2008,(16):5031-5037.doi:10.1038/cdd.2009.35.

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