Literature DB >> 19393553

Improvement of FR901379 production by mutant selection and medium optimization.

Munekazu Kanda1, Masaru Tsuboi, Kazutoshi Sakamoto, Shiho Shimizu, Michio Yamashita, Hiroyuki Honda.   

Abstract

FR901379 (WF11899A) is a novel echinocandin type of lipopeptide antibiotic produced by Coleophoma empetri F-11899. Micafungin (FK463) is derived from the chemical modification of deacylated FR901379. In the present paper, we performed seven generation's strain-breeding, beginning with a wild type, was performed. Selection medium for screening and production medium for high FR901379 production were designed. Sodium chloride content in the selection plate was affected to FR901379 production and shrinkage of the colony size was observed in high producing strains. As selection markers, large colony-shrinking rate and large inhibition circle in the agar-piece method using C. albicans was selected. Using CMA medium with high sodium chloride, 3 mutants, M-1 to M-3, have achieved a high FR901379 production and M-3 showed 5.0 U/mL, while 1.0 U/mL of production was achieved in wild type strain. A-2 medium supplemented with 6% of soluble starch as a carbon source and 0.6% of ammonium sulfate as nitrogen source was also further effective for mutant screening. The FR901379 production of mutant M-4 (fourth generation) increased until 16.0 U/mL. The concentration of the phosphate salt in the medium seemed to inhibit the growth so as to extend the culture period. When the A-3 medium supplemented with low concentration of phosphate salt and magnesium sulfate as a sulfate source was designed and used, mutants with improved production were successively obtained. Finally, variant strain M-7 showed 30.0 U/mL of production, which was about 30 times higher than that of the wild strain.

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Year:  2009        PMID: 19393553     DOI: 10.1016/j.jbiosc.2009.01.002

Source DB:  PubMed          Journal:  J Biosci Bioeng        ISSN: 1347-4421            Impact factor:   2.894


  2 in total

1.  Integrated strategy of temperature shift and mannitol feeding for enhanced production of echinocandin B by Aspergillus nidulans CCTCC M2012300.

Authors:  Shu-Ping Zou; Yan Xiong; Kun Niu; Zhong-Ce Hu; Yu-Guo Zheng
Journal:  3 Biotech       Date:  2019-03-14       Impact factor: 2.406

Review 2.  Echinocandins: structural diversity, biosynthesis, and development of antimycotics.

Authors:  Wolfgang Hüttel
Journal:  Appl Microbiol Biotechnol       Date:  2020-12-03       Impact factor: 4.813

  2 in total

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