Abstract

Actinomycetes populate soils and aquatic sediments that impose biotic and abiotic challenges for their survival. As a result, actinomycetes metabolism and genomes have evolved to produce an overwhelming diversity of specialized molecules. Polyketides, non-ribosomal peptides, post-translationally modified peptides, lactams, and terpenes are well-known bioactive natural products with enormous industrial potential. Accessing such biological diversity has proven difficult due to the complex regulation of cellular metabolism in actinomycetes and to the sparse knowledge of their physiology. The past decade, however, has seen the development of omics technologies that have significantly contributed to our better understanding of their biology. Key observations have contributed toward a shift in the exploitation of actinomycete’s biology, such as using their full genomic potential, activating entire pathways through key metabolic elicitors and pathway engineering to improve biosynthesis. Here, we review recent efforts devoted to achieving enhanced discovery, activation, and manipulation of natural product biosynthetic pathways in model actinomycetes using genome-scale biological datasets.

Highlights

  • Actinomycetes represent one of the largest bacterial phyla and are primary contributors to carbon cycling and a major source of bioactive natural products (BNP) including, most prominently, antibiotics

  • The genomic space for in silico genome annotation pipelines is biased for certain G + C content sequences, gene length, and organization

  • Approximately 60% of the bacterial genomic space is missannotated in terms of gene boundaries caused by minimal cross-checks between computationally assigned open-reading frames (ORFs) and real genes (Nielsen and Krogh, 2005)

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Summary

Systems Biology Approaches to Understand natural Products Biosynthesis

Cuauhtemoc Licona-Cassani1,2 , Pablo Cruz-Morales , Angel Manteca , Francisco Barona-Gomez , Lars K. Systems Biology Approaches to Understand Natural Products Biosynthesis. Polyketides, non-ribosomal peptides, post-translationally modified peptides, lactams, and terpenes are well-known bioactive natural products with enormous industrial potential. Accessing such biological diversity has proven difficult due to the complex regulation of cellular metabolism in actinomycetes and to the sparse knowledge of their physiology. Key observations have contributed toward a shift in the exploitation of actinomycete’s biology, such as using their full genomic potential, activating entire pathways through key metabolic elicitors and pathway engineering to improve biosynthesis. We review recent efforts devoted to achieving enhanced discovery, activation, and manipulation of natural product biosynthetic pathways in model actinomycetes using genome-scale biological datasets

INTRODUCTION
Genome Mining and Pathway Discovery
Physiological Transitions and Development
Findings
FUTURE DIRECTIONS
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