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Omics based approach for biodiscovery of microbial natural products in antibiotic resistance era

机译:基于组学的方法在抗生素抗药性时代对微生物天然产物进行生物发现

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摘要

The need for a new antibiotic pipeline to confront threat imposed by resistant pathogens has become a major global concern for human health. To confront the challenge there is a need for discovery and development of new class of antibiotics. Nature which is considered treasure trove, there is re-emerged interest in exploring untapped microbial to yield novel molecules, due to their wide array of negative effects associated with synthetic drugs. Natural product researchers have developed many new techniques over the past few years for developing diverse compounds of biopotential. Taking edge in the advancement of genomics, genetic engineering, in silico drug design, surface modification, scaffolds, pharmacophores and target-based approach is necessary. These techniques have been economically sustainable and also proven efficient in natural product discovery. This review will focus on recent advances in diverse discipline approach from integrated Bioinformatics predictions, genetic engineering and medicinal chemistry for the synthesis of natural products vital for the discovery of novel antibiotics having potential application.
机译:需要一种新的抗生素管道来对抗由耐药菌引起的威胁,这已成为全球人类健康的主要问题。面对挑战,需要发现和开发新型的抗生素。自然界被认为是宝库,由于它们与合成药物相关的广泛的负面影响,人们对探索未开发的微生物以产生新分子的兴趣再次出现。过去几年,天然产物研究人员开发了许多新技术来开发多种生物电势化合物。必须在基因组学,基因工程,计算机药物设计,表面修饰,支架,药效团和基于靶标的方法方面取得优势。这些技术在经济上是可持续的,并且在天然产物发现中也被证明是有效的。这篇综述将聚焦于从综合的生物信息学预测,基因工程和药物化学等多种学科方法的最新进展,这些方法对于发现具有潜在应用潜力的新型抗生素至关重要的天然产物的合成。

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