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Journal Abstract Search

140 related items for PubMed ID: 2010360

  • 1. Microbial conversion of milbemycins: hydroxylation of milbemycin A4 and related compounds by Cunninghamella echinulata ATCC 9244.
    Nakagawa K, Miyakoshi S, Torikata A, Sato K, Tsukamoto Y.
    J Antibiot (Tokyo); 1991 Feb; 44(2):232-40. PubMed ID: 2010360
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  • 2. Microbial conversion of milbemycins: 30-oxidation of milbemycin A4 and related compounds by Amycolata autotrophica and Amycolatopsis mediterranei.
    Nakagawa K, Torikata A, Sato K, Tsukamoto Y.
    J Antibiot (Tokyo); 1990 Oct; 43(10):1321-8. PubMed ID: 2258330
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  • 3. Microbial conversion of milbemycins: oxidation of milbemycin A4 and related compounds at the C-25 ethyl group by Circinella umbellata and Absidia cylindrospora.
    Nakagawa K, Tsukamoto Y, Sato K, Torikata A.
    J Antibiot (Tokyo); 1995 Aug; 48(8):831-7. PubMed ID: 7592029
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  • 4. Bioconversion of milbemycin-related compounds: biosynthetic pathway of milbemycins.
    Nonaka K, Kumasaka C, Okamoto Y, Maruyama F, Yoshikawa H.
    J Antibiot (Tokyo); 1999 Feb; 52(2):109-16. PubMed ID: 10344564
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  • 5. Milbemycins alpha 11, alpha 12, alpha 13, alpha 14 and alpha 15: a new family of milbemycins from Streptomyces hygroscopicus subsp. aureolacrimosus. Taxonomy, fermentation, isolation, structure elucidation and biological properties.
    Takahashi S, Miyaoka H, Tanaka K, Enokita R, Okazaki T.
    J Antibiot (Tokyo); 1993 Sep; 46(9):1364-71. PubMed ID: 8226315
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  • 7. Bioconversion of milbemycin-related compounds: isolation and utilization of non-producer, strain RNBC-5-51.
    Nonaka K, Tsukiyama T, Sato K, Kumasaka C, Maruyama F, Yoshikawa H.
    J Antibiot (Tokyo); 1999 Jul; 52(7):620-7. PubMed ID: 10513841
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  • 9. Genetic engineering of Streptomyces bingchenggensis to produce milbemycins A3/A4 as main components and eliminate the biosynthesis of nanchangmycin.
    Zhang J, An J, Wang JJ, Yan YJ, He HR, Wang XJ, Xiang WS.
    Appl Microbiol Biotechnol; 2013 Dec; 97(23):10091-101. PubMed ID: 24077727
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  • 11. Hydroxylation of the native brassinosteroids 24-epicastasterone and 24-epibrassinolide by the fungus Cunninghamella echinulata.
    Voigt B, Porzel A, Naumann H, Hörhold-Schubert C, Adam G.
    Steroids; 1993 Jul; 58(7):320-3. PubMed ID: 8212079
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  • 12. Combined application of plasma mutagenesis and gene engineering leads to 5-oxomilbemycins A3/A4 as main components from Streptomyces bingchenggensis.
    Wang HY, Zhang J, Zhang YJ, Zhang B, Liu CX, He HR, Wang XJ, Xiang WS.
    Appl Microbiol Biotechnol; 2014 Dec; 98(23):9703-12. PubMed ID: 25081559
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  • 15. Mechanism of hydroxylation of biphenyl by Cunninghamella echinulata.
    Smith RV, Davis PJ, Clark AM, Prasatik SK.
    Biochem J; 1981 Apr 15; 196(1):369-71. PubMed ID: 7306077
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  • 19. Synthesis of Novel 25-Substituted Milbemycin A4 Derivatives and Their Acaricidal Activity against Tetranychus urticae.
    Tsukamoto Y, Nakagawa H, Kajino H, Sato K, Tanaka K, Yanai T.
    Biosci Biotechnol Biochem; 1997 Jan 15; 61(10):1650-7. PubMed ID: 27393161
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  • 20. Engineered biosynthesis of milbemycins in the avermectin high-producing strain Streptomyces avermitilis.
    Kim MS, Cho WJ, Song MC, Park SW, Kim K, Kim E, Lee N, Nam SJ, Oh KH, Yoon YJ.
    Microb Cell Fact; 2017 Jan 17; 16(1):9. PubMed ID: 28095865
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