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从 Juniperus excelsa 的根际土壤中筛选产生噻二唑类化合物的链霉菌。

Screening of Thiopeptide-Producing Streptomycetes Isolated From the Rhizosphere Soil of Juniperus excelsa.

机构信息

Department of Genetics and Biotechnology, Ivan Franko National University of Lviv, Lviv, 79005, Ukraine.

Department of Pharmaceutical Biotechnology, Saarland University, 66123, Saarbruecken, Germany.

出版信息

Curr Microbiol. 2022 Sep 5;79(10):305. doi: 10.1007/s00284-022-03004-2.

Abstract

The identification of an increasing number of drug-resistant pathogens has stimulated the development of new therapeutic agents to combat them. Microbial natural products are among the most important elements when it comes to drug discovery. Today, thiopeptide antibiotics are receiving increasing research attention due to their potent activity against Gram-positive bacteria. In this study, we demonstrated the successful use of a whole-cell microbial biosensor (Streptomyces lividans TK24 pMO16) for the specific detection of thiopeptide antibiotics among the native actinomycete strains isolated from the rhizosphere soil of Juniperus excelsa (Bieb.). Among the native strains, two strains of Streptomyces, namely sp. Je 1-79 and Je 1-613, were identified that were capable of producing thiopeptide antibiotics. A multilocus sequence analysis of five housekeeping genes (gyrB, atpD, recA, rpoB, and trpB) classified them as representatives of two different species of the genus Streptomyces. The thiopeptide antibiotics berninamycin A and B were identified in the extracts of the two strains by means of a dereplication analysis. The berninamycin biosynthetic gene cluster was also detected in the genome of the Streptomyces sp. Je 1-79 strain and showed a high level of similarity (93%) with the ber cluster from S. bernensis. Thus, the use of this whole-cell biosensor during the first stage of the screening process could serve to accelerate the specific detection of thiopeptide antibiotics.

摘要

越来越多的耐药病原体的鉴定刺激了新治疗药物的开发,以对抗它们。微生物天然产物是药物发现中最重要的元素之一。如今,由于其对革兰氏阳性菌的有效活性,硫肽抗生素受到越来越多的研究关注。在这项研究中,我们成功地使用了一种全细胞微生物生物传感器(紫色链霉菌 TK24 pMO16),用于从 Juniperus excelsa(Bieb.)根际土壤中分离的天然放线菌菌株中特异性检测硫肽抗生素。在天然菌株中,鉴定出两种能够产生硫肽抗生素的链霉菌,即 sp. Je 1-79 和 Je 1-613。五个看家基因(gyrB、atpD、recA、rpoB 和 trpB)的多位序列分析将它们分类为链霉菌属的两个不同种的代表。通过去重复分析,在这两种菌株的提取物中鉴定出了伯宁霉素 A 和 B。在 Streptomyces sp. Je 1-79 菌株的基因组中也检测到了伯宁霉素生物合成基因簇,与 S. bernensis 中的 ber 簇具有高度相似性(93%)。因此,在筛选过程的第一阶段使用这种全细胞生物传感器可以加速硫肽抗生素的特异性检测。

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