Singh Tanim Arpit, Passari Ajit Kumar, Jajoo Anjana, Bhasin Sheetal, Gupta Vijai Kumar, Hashem Abeer, Alqarawi Abdulaziz A, Abd Allah Elsayed Fathi
Department of Biosciences, Maharaja Ranjit Singh College of Professional Sciences, Indore, India.
School of Life Sciences, Devi Ahilya Vishwavidyalaya, Indore, India.
Front Microbiol. 2021 Jun 22;12:655620. doi: 10.3389/fmicb.2021.655620. eCollection 2021.
The presence of secondary metabolite biosynthetic gene clusters (BGCs) makes actinobacteria well-known producers of diverse metabolites. These ubiquitous microbes are extensively exploited for their ability to synthesize diverse secondary metabolites. The extent of their ability to synthesize various molecules is yet to be evaluated. Current advancements in genome sequencing, metabolomics, and bioinformatics have provided a plethora of information about the mechanism of synthesis of these bioactive molecules. Accessing the biosynthetic gene cluster responsible for the production of metabolites has always been a challenging assignment. The genomic approach developments have opened a new gateway for examining and manipulating novel antibiotic gene clusters. These advancements have now developed a better understanding of actinobacterial physiology and their genetic regulation for the prolific production of natural products. These new approaches provide a unique opportunity to discover novel bioactive compounds that might replenish antibiotics' exhausted stock and counter the microbes' resistance crisis.
次生代谢物生物合成基因簇(BGCs)的存在使放线菌成为众所周知的多种代谢物生产者。这些无处不在的微生物因其合成多种次生代谢物的能力而被广泛利用。它们合成各种分子的能力程度尚待评估。基因组测序、代谢组学和生物信息学的当前进展提供了大量有关这些生物活性分子合成机制的信息。获取负责代谢物产生的生物合成基因簇一直是一项具有挑战性的任务。基因组方法的发展为检查和操纵新型抗生素基因簇开辟了新途径。这些进展现在使人们对放线菌生理学及其对天然产物大量生产的遗传调控有了更好的理解。这些新方法提供了一个独特的机会来发现新型生物活性化合物,这些化合物可能补充抗生素已枯竭的储备并应对微生物的耐药性危机。