|
|
Screening of excellent strains derived from 7 β,15 α-dihydroxy-18β- glycyrrhetinic acid by microbial transformation |
MA Yuan1 SUN Peng2 WANG Heng3 LI Zhuofan3 CHEN Gang4 SHI Minghui4 |
1.Key Laboratory of Uygur Medicines, Xinjiang Uygur Autonomous Region Institute of Materia Medica, Xinjiang Uygur Autonomous Region, Urumqi 830004, China;
2.Medical Device Testing Center, Xinjiang Institutes of Drug Control, Xinjiang Uygur Autonomous Region, Urumqi 830054, China;
3.Department of Traditional Chinese Medicine, College of Pharmacy, Shihezi University, Xinjiang Uygur Autonomous Region, Shihezi 832000, China; 4.Analysis and Testing Center, Xinjiang Uygur Autonomous Region Institute of Traditional Chinese Medica and National Medica, Xinjiang Uygur Autonomous Region, Urumqi 830002, China
|
|
|
Abstract Objective To screen the excellent strains through microbial transformation, using 7β,15α-dihydroxy-18β- glycyrrhetinic acid as the target product. Methods Ten fungi (CGMCC 3.149, CGMCC 3.193, CGMCC 3.3402, CGMCC 3.739, CGMCC 3.2462, CGMCC 3.2886, CGMCC 3.3400, CGMCC 3.577, CGMCC 3.970, and Zw-4) were used for preliminary screening and re-screening experiments of transformed strains, the content of 7β,15α-dihydroxy-18β-glycyrrhetinic acid in the converted liquid was determined by high performance liquid chromatography. The conversion rate of 7β,15α-dihydroxy-18β-glycyrrhetinic acid was used as the evaluation index and the strains with high conversion rate and consistent results of preliminary screening and re-screening experiments were selected as the excellent strains. 7β,15α-dihydroxy- 18β-glycyrrhetinic acid showed a good linear relationship in the range of 2.56~81.79 μg/ml. The strain with the highest conversion rate of preliminary screening experiment was CGMCC 3.3400. The strain with the highest conversion rate of re-screening experiment was CGMCC 3.970. Conclusion The excellent strain is CGMCC 3.970.
|
|
|
|
|
[1] 赵欢.甘草次酸及其衍生物的抗炎活性研究及应用[D].天津:天津科技大学,2020.
[2] Moustafa GO,Shalaby Ahmed,Naglah AM,et al. Synthesis,characterization,in vitro anticancer potentiality,and antimicrobial activities of novel peptide-glycyrrhetinic-acid-based derivatives [J]. Molecules,2021,26(15):4573.
[3] 高丰,周菲,陈红珊,等.甘草次酸抗肿瘤衍生物的设计、合成及其活性评价[J].西北药学杂志,2021,36(5):789-796.
[4] 张丽娟,喻红梅,张勇,等.甘草次酸纳米粒的制备、表征及其抗肿瘤活性研究[J].中国药房,2020,31(13):1589- 1594.
[5] 李志健.裂-A-五环三萜衍生物的合成及其体外抗HBV活性研究[D].广州:南方医科大学,2018.
[6] Chen F,Zhang KX,Jia L,et al. Synthesis and anti-HCV activities of 18β-glycyrrhetinic acid derivatives and their In-silico ADMET analysis [J]. Curr Comput Aided Drug Des, 2021,17(6):831-837.
[7] 张伟.甘草次酸的提取、结构修饰及降血糖活性研究[D].天津:天津科技大学,2020.
[8] 刘靖丽,闫浩,王钰莹,等.甘草皂苷类化合物结构与保肝活性关系的DFT研究[J].天然产物研究与开发,2020, 32(9):1515-1521.
[9] 刘文静,南一,鲁玉梅,等.甘草次酸对kk-Ay糖尿病小鼠早中期肾纤维化的保护作用[J].云南中医中药杂志,2020,41(3):72-78.
[10] 左家伟.新型甘草次酸脲类化合物的设计、合成及其对急性肾损伤的治疗作用[D].合肥:安徽医科大学,2021.
[11] 向猛.含异丙醇胺亚结构的新型甘草次酸衍生物的合成及生物活性研究[D].贵阳:贵州大学,2020.
[12] 阮仁余,徐静怡,马宇春,等.甘草次酸抑菌免洗洗手液的研制[J].科技视界,2020(12):71-73.
[13] Zhang Q,Xiong YS,Cheng JX,et al. Synthesis and biological evaluation of ruthenium polypyridine complexes with 18β-glycyrrhetinic acid as antibacterial agents against Staphylococcus aureus [J]. Dalton Trans,2022,51(3):1099- 1111.
[14] 马媛,石明辉,戴均贵,等.18β-甘草次酸的结构修饰及生物活性研究进展[J].西北药学杂志,2018,33(4):563-567.
[15] 张光辉,龙旭,张拴,等.甘草次酸的结构修饰及生物活性研究进展[J].当代化工,2020(2):393-397.
[16] 赵子璇,李春峰,杨洪旺,等.五环三萜类化合物微生物转化研究进展[J].天然产物研究与开发,2021,33(8):1415-1426.
[17] 王志琪,张序晴,王尚尧,等.基于化学、体内过程和代谢组学的甘草解毒作用研究概况[J].湖南中医药大学学报,2019,39(1):132-137.
[18] 罗子宸,张雯,杨瑞,等.甘草“调和诸药”生物药剂学机制的研究进展[J].中草药,2021,52(1):267-277.
[19] 李立文,张嘉丽,董杨,等.甘草酸、甘草次酸假性醛固酮作用和药物相互作用研究进展[J].辽宁中医药大学学报,2018,20(10):216-220.
[20] 马媛.甘草次酸的微生物转化研究[D].乌鲁木齐:新疆医科大学,2015.
[21] Ma Y,Liu JM,Chen RD,et al. Microbial transformation of glycyrrhetinic acid and potent neural anti-inflammatory activity of the metabolites [J]. Chin Chem Lett,2017,28(6): 1200-1204.
[22] 苏龙,梁广波,陈光丽,等.甘草酸微生物转化菌的筛选鉴定及发酵条件优化[J].湖北农业科学,2017,56(10):1918-1923.
[23] 和朝军,孙华,李鹏举,等.新月弯孢霉KA-91对甘草次酸的转化研究[J].药物生物技术,2011,18(3):238-241.
[24] 赵文俊,吴嘉南,何国庆,等.甘草次酸生物合成菌株的筛选与发酵条件优化[J].中国食品学报,2020,20(5):113-119.
[25] 王照华.传统中药厚朴主要成分厚朴酚与和厚朴酚的微生物转化[D].北京:中央民族大学,2013. |
|
|
|