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首页> 外文期刊>RSC Advances >Microbial transformations of 4-methylchalcones as an efficient method of obtaining novel alcohol and dihydrochalcone derivatives with antimicrobial activity
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Microbial transformations of 4-methylchalcones as an efficient method of obtaining novel alcohol and dihydrochalcone derivatives with antimicrobial activity

机译:4-甲基凝块的微生物转化为具有抗微生物活性的新型醇和二氢酮衍生物的有效方法

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摘要

Biotransformations are an alternative method of receiving dihydrochalcones as a result of the reduction of ,-unsaturated ketones - chalcones. In presented research, two strains of bacteria - Gordonia sp. DSM44456 and Rhodococcus sp. DSM364 - were selected as effective biocatalysts that are able to transform chalcones in a short period of time. As a result of our investigation 3 new dihydrochalcones and one novel alcohol were obtained with high isolated yields. All 4-methylchalcone derivatives and biotransformations products were tested for antimicrobial activity against Escherichia coli ATCC10536, Staphylococcus aureus DSM799, Candida albicans DSM1386, Alternaria alternata CBS1526, Fusarium linii KB-F1, and Aspergillus niger DSM1957. The best inhibitory effect was observed for all chalcones against E. coli ATCC10536 - compounds 1-6 and 8 prevented thorough growth of this strain (OD = 0). Moreover, dihydrochalcones showed about 2-3 times stronger inhibitory effect against S. aureus DSM799 in comparison to their chalcones. Excluding the E. coli ATCC10536 strain, 3-(4-carboxyphenyl)-1-(4-methylphenyl)propan-1-ol (8b) had weaker biological activity than 4-carboxy-4-methyl-,-dihydrochalcone (8a).
机译:生物转化是由于减少 - 不饱和酮 - 杀牛酮而接受二羟基葡萄酒的另一种方法。在提出的研究中,两种细菌菌株 - 戈登菊属植物。 dsm44456和rhodococcus sp。 DSM364 - 被选为有效的生物催化剂,可以在短时间内改变杀碎机。由于我们的研究,3种新的二羟基葡萄酒和一种新的醇以高分离的产率获得。所有4-甲基丙酮衍生物和生物转化产物对Escherichia Coli ATCC10536,念珠菌AGICUS DSM799,Candida albicans DSM1526,Fusarium Linii Kb-F1和Aspergillus Niger DSM1957进行了测试的所有4-甲基丙酮衍生物和生物转化物。针对E. Coli ATCC10536 - 化合物1-6和8的所有Chalcone观察到最佳抑制效果,防止了该菌株的彻底生长(OD = 0)。此外,与其丘氨酸相比,二羟基酮与S.UUREUS DSM799的抑制作用较高约2-3倍。不包括大肠杆菌ATCC10536菌株,3-(4-羧基苯基)-1-(4-甲基苯基)丙烷-1-醇(8b)具有比4-羧基-4-甲基 - - 二氢丙酮(8a)的生物活性较弱。

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  • 来源
    《RSC Advances》 |2018年第53期|共8页
  • 作者单位

    Wroclaw Univ Environm &

    Life Sci Dept Chem Norwida 25 PL-50375 Wroclaw Poland;

    Wroclaw Univ Environm &

    Life Sci Dept Chem Norwida 25 PL-50375 Wroclaw Poland;

    Wroclaw Univ Environm &

    Life Sci Dept Biotechnol &

    Food Microbiol Chelmonskiego 37 PL-51630 Wroclaw Poland;

    Wroclaw Univ Environm &

    Life Sci Dept Chem Norwida 25 PL-50375 Wroclaw Poland;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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