从药用植物 Anthemis pseudocotula Boiss.

Q3 Veterinary
Archives of Razi Institute Pub Date : 2023-10-31 eCollection Date: 2023-10-01 DOI:10.22092/ARI.2023.78.5.1638
Hajizadeh Maryam, Pourahmad Fazel, Nemati Mostafa
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引用次数: 0

摘要

抗生素耐药性在全球范围内急剧上升,因此生产新的抗生素是必不可少的。近期的科学研究主要集中在微生物次生代谢物的生物勘探方面,尤其注重从内生菌中寻找具有抗菌特性的天然产品。所有植物物种,无论其类型如何,都被认为锚定有内生细菌(EB)。由 EB 制造的天然治疗化合物在医学、农业和制药业中有许多潜在用途。为了研究 EB 的抗菌特性,本研究从 Anthemis pseudocotula Boiss.中分离出放线菌(原放线菌),对其进行鉴定,并通过形态学和分子学方法对其进行生物勘测。样本从伊朗伊拉姆采集,然后分成根、叶、茎和花。消毒后切成 2 毫米的小块,在酪蛋白琼脂培养基上培养,并在 28ºC 温度下培养长达四周。放线菌用 16S rRNA 基因聚合酶链反应法进行鉴定。为了评估分离出的放线菌群的抗菌特性,采用了琼脂扩散法。同时,还测定了分离的放线菌群中生物合成基因簇的频率,包括多酮合成酶(PKS-I 和 PKS-II)和非核糖体肽合成酶(NRPS)基因。从 Anthemis 花的不同部位分离出 90 种细菌。其中 38 个细菌(42.2%)属于放线菌门,在这 38 个细菌中,15 个分离菌(39.5%)具有抗菌特性。其中,11 个分离物(73.3%)对金黄色葡萄球菌有抗菌作用,2 个分离物(13.3%)对铜绿假单胞菌有抗菌作用,3 个分离物(20%)对大肠杆菌有抗菌作用,2 个分离物(13.3%)对伤寒沙门氏菌亚种有抗菌作用。PKS-I、PKS-II 和 NRPS 基因的分子分析结果显示,在 38 株分离的放线菌中,23 株(60.5%)携带 PKS-I 基因,6 株(15.8%)携带 PKS-II 基因,20 株(52.6%)携带 NRPS 基因。这项研究表明,Anthemis pseudocotula Boiss.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation and Screening of Antibacterial Activity of Actinomycetota from the Medicinal Plant, Anthemis pseudocotula Boiss.

Antibiotic resistance is rising dramatically worldwide, and thus the production of new antibiotics is indispensable. Recent scientific initiatives have focused on the bioprospecting of microorganisms' secondary metabolites, with a particular focus on the look for natural products with antimicrobial properties derived from endophytes. All plant species, regardless of their type, are thought to anchor endophytic bacteria (EB). There are many potential uses for the natural therapeutic compounds made by EB in medicine, agriculture, and the pharmaceutical industry. To investigate antibacterial properties in this study, Actinomycetota (formerly, Actinobacteria) were isolated from Anthemis pseudocotula Boiss., identified, and underwent bioprospecting by morphological and molecular methods. Samples were collected from Ilam, Iran, and then divided into roots, leaves, stems, and flowers. After disinfection, they were cut into 2 mm pieces, cultured on casein agar culture medium, and incubated at 28ºC for up to four weeks. Actinomycetota was identified using the polymerase chain reaction method targeting the 16S rRNA gene. To evaluate the antibacterial properties of the isolated Actinomycetota, the agar diffusion method was used. In parallel, the frequencies of biosynthetic gene clusters, including polyketide synthase (PKS-I and PKS-II) and nonribosomal peptide synthetase (NRPS) genes, were determined in the isolated Actinomycetota. Ninety bacteria were isolated from different parts of Anthemis flowers. Thirty-eight (42.2%) of these bacteria belonged to the phylum Actinomycetota, and out of these 38, 15 isolates (39.5%) had antibacterial properties. Of these, 11 isolates (73.3%) exhibited antibacterial effects against Staphylococcus aureus, 2 (13.3%) against Pseudomonas aeruginosa, 3 (20%) against Escherichia coli, and two isolates (13.3%) against Salmonella enterica sub-species of enterica serovar Typhimurium. The results of the molecular analysis of PKS-I, PKS-II, and NRPS genes showed that out of 38 isolated Actinomycetota strains, 23 isolates (60.5%) carried PKS-I gene, 6 (15.8%) harbored PKS-II gene, and 20 isolates (52.6%) had NRPS gene. This study indicates that Anthemis pseudocotula Boiss. has a number of active Actinomycetota that produce secondary metabolites with antibacterial properties.

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Archives of Razi Institute
Archives of Razi Institute Veterinary-Veterinary (all)
CiteScore
1.50
自引率
0.00%
发文量
108
审稿时长
12 weeks
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