决明子皮皂素-多溴酚抗生素(CU1)抗RNA聚合酶多重耐药细菌

Q2 Agricultural and Biological Sciences Current Research in Pharmacology and Drug Discovery Pub Date : 2022-01-01 DOI:10.1016/j.crphar.2022.100090
Asit Kumar Chakraborty , Sourajit Saha , Kousik Poria , Tanmoy Samanta , Sudhanshu Gautam , Jayanta Mukhopadhyay
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引用次数: 3

摘要

随着耐多药质粒获得10个耐多药和药物外排基因来灭活抗生素,耐多药感染的逐渐增加对人类构成了威胁。植物分泌抗代谢物来延缓土壤和水中细菌的生长,是抗生素的理想来源。目的从印度药用植物中发现一种选择性杀灭耐多药细菌的替代植物药。方法从恒河水、牛奶、鸡肉和人发中分离smdr细菌,对植物提取物进行检测。对80种药用植物进行了筛选,筛选出6种具有良好抗菌活性的植物提取物,经琼脂孔测定,裂解区大于15 mm。植物提取物在乙醇或甲醇(1:5 w/v)中制备过夜并浓缩。采用制备层析和高效液相色谱法进行植物化学纯化。采用质谱、核磁共振、红外光谱等方法对CU1进行了化学分析。采用体外RNA聚合酶和DNA聚合酶测定进行靶标鉴定。结果cu1为结构较大的皂苷溴多酚类化合物,在HPLC C18柱3min纯化。在琼脂孔试验中,CU1具有杀菌作用,但活性比利福平低三倍。而在LB培养基中,由于溶解度问题,表现出15倍以上的差抑制剂。CU1抑制大肠杆菌和结核分枝杆菌RNA聚合酶的转录。凝胶位移实验表明,CU1干扰了开放启动子复合物的形成步骤。另一方面,CU1不抑制DNA聚合酶。结论决明子皮植物化学物质丰富、毒性小、靶向性强,可能是一种更安全、低成本的耐多药细菌性疾病治疗药物。
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A saponin-polybromophenol antibiotic (CU1) from Cassia fistula Bark Against Multi-Drug Resistant Bacteria Targeting RNA polymerase

Background

Gradual increase of multidrug resistant infections is a threat to the human race as MDR plasmids have acquired.>10 mdr and drug efflux genes to inactivate antibiotics. Plants secret anti-metabolites to retard growth of soil and water bacteria and are ideal source of antibiotics.

Purpose

Purpose of the study is to discover an alternate phyto-drug from medicinal plants of India that selectively kills MDR bacteria.

Methods

MDR bacteria isolated from Ganga river water, milk, chicken meat and human hair for testing phyto-extracts. Eighty medicinal plants were searched and six phyto-extracts were selected having good antibacterial activities as demonstrated by agar-hole assays giving 15 ​mm or greater lysis zone. Phyto-extracts were made in ethanol or methanol (1:5 w/v) for overnight and were concentrated. Preparative TLC and HPLC were performed to purify phytochemical. MASS, NMR, FTIR methods were used for chemical analysis of CU1. In vitro RNA polymerase and DNA polymerase assays were performed for target identification.

Results

CU1 belongs to a saponin bromo-polyphenol compound with a large structure that purified on HPLC C18 column at 3min. CU1 is bacteriocidal but three times less active than rifampicin in Agar-hole assay. While in LB medium it shows greater than fifteen times poor inhibitor due to solubility problem. CU1 inhibited transcription from Escherichia coli as well as Mycobacterium tuberculosis RNA Polymerases. Gel shift assays demonstrated that CU1 interferes at the open promoter complex formation step. On the other hand CU1 did not inhibit DNA polymerase.

Conclusion

Phyto-chemicals from Cassia fistula bark are abundant, less toxic, target specific and may be a safer low cost drug against MDR bacterial diseases.

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来源期刊
Current Research in Pharmacology and Drug Discovery
Current Research in Pharmacology and Drug Discovery Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
6.40
自引率
0.00%
发文量
65
审稿时长
40 days
期刊最新文献
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