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具有抗菌活性的内生细菌菌株EP1的生物活性化合物

Bioactive Compounds from Endophytic Bacteria Strain EP1 with Their Antibacterial Activities.

作者信息

Numan Muhammad, Shah Muddaser, Asaf Sajjad, Ur Rehman Najeeb, Al-Harrasi Ahmed

机构信息

Natural & Medical Sciences Research Center, University of Nizwa, Nizwa 616, Oman.

Department of Biology, University of North Carolina at Greensboro, Greensboro, NC 27412, USA.

出版信息

Metabolites. 2022 Dec 7;12(12):1228. doi: 10.3390/metabo12121228.

DOI:10.3390/metabo12121228
PMID:36557265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9788538/
Abstract

Endophytic bacteria boost host plant defense and growth by producing vital compounds. In the current study, a bacterial strain was isolated from the plant and identified as strain EP1 (accession number: MT256301) through 16S RNA gene sequencing. From the identified bacteria, four compounds- (4-(4-cinnamoyloxy)phenyl)butanoic acid), (cyclo-(L-Pro-D-Tyr)), (cyclo-(L-Val-L-Phe)), and (cyclo-(L-Pro-L-Val))-were isolated and characterized by 1D and 2D NMR and mass spectroscopy. Moreover, antibacterial activity and beta-lactam-producing gene inhibition (δ-(l-α-aminoadipyl)-l-cysteinyl-d-valine synthetase (ACVS) and aminoadipate aminotransferase (AADAT)) assays were performed. Significant antibacterial activity was observed against the human pathogenic bacterial strains () by compound with a 13 ± 0.7 mm zone of inhibition (ZOI), followed by compound having an 11 ± 0.7 mm ZOI. In contrast, the least antibacterial activity among the tested samples was offered by compound with a 10 ± 0.9 mm ZOI compared to the standard (26 ± 1.2 mm). Similarly, the molecular analysis of beta-lactam inhibition determined that compounds and inhibited the two genes (2- to 4-fold) in the beta-lactam biosynthesis (ACVS and AADAT) pathway. From these results, it can be concluded that future research on these compounds could lead to the inhibition of antibiotic-resistant pathogenic bacterial strains.

摘要

内生细菌通过产生重要化合物来增强宿主植物的防御能力和促进生长。在本研究中,从植物中分离出一株细菌,并通过16S rRNA基因测序将其鉴定为EP1菌株(登录号:MT256301)。从鉴定出的细菌中,分离出四种化合物——(4-(4-肉桂酰氧基)苯基)丁酸、环(L-脯氨酸-D-酪氨酸)、环(L-缬氨酸-L-苯丙氨酸)和环(L-脯氨酸-L-缬氨酸),并通过一维和二维核磁共振以及质谱对其进行了表征。此外,还进行了抗菌活性和β-内酰胺产生基因抑制(δ-(L-α-氨基己二酰基)-L-半胱氨酰-D-缬氨酸合成酶(ACVS)和氨基己二酸氨基转移酶(AADAT))测定。化合物对人类致病细菌菌株表现出显著的抗菌活性,抑菌圈直径为13±0.7毫米,其次是化合物,抑菌圈直径为11±0.7毫米。相比之下,与标准品(26±1.2毫米)相比,化合物的抑菌圈直径为10±0.9毫米,在所测试的样品中抗菌活性最低。同样,β-内酰胺抑制的分子分析确定,化合物和抑制了β-内酰胺生物合成(ACVS和AADAT)途径中的两个基因(2至4倍)。从这些结果可以得出结论,对这些化合物的未来研究可能会导致对抗生素耐药的致病细菌菌株的抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7bb/9788538/fc0ed9bd0635/metabolites-12-01228-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7bb/9788538/e3ebfb5b1858/metabolites-12-01228-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7bb/9788538/b9fcbfd219f4/metabolites-12-01228-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7bb/9788538/fc0ed9bd0635/metabolites-12-01228-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7bb/9788538/e3ebfb5b1858/metabolites-12-01228-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7bb/9788538/b9fcbfd219f4/metabolites-12-01228-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7bb/9788538/fc0ed9bd0635/metabolites-12-01228-g003.jpg

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