scholarly journals A chromatogram-simplified Streptomyces albus host for heterologous production of natural products

2019 ◽  
Author(s):  
Asif Fazal ◽  
Divya Thankachan ◽  
Ellie Harris ◽  
Ryan F. Seipke
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Gene Clusters ◽  
Heterologous Production ◽  
Biosynthetic Gene ◽  
Critical Aspect ◽  
Biosynthetic Gene Clusters ◽  
Streptomyces Albus ◽  
Microbial Natural Products ◽  
Suitable Expression

AbstractCloning natural product biosynthetic gene clusters from cultured or uncultured sources and their subsequent expression by genetically tractable heterologous hosts is an essential strategy for the elucidation and characterisation of novel microbial natural products. The availability of suitable expression hosts is a critical aspect of this workflow. In this work, we mutagenised five endogenous biosynthetic gene clusters from Streptomyces albus S4, which reduced the complexity of chemical extracts generated from the strain and eliminated antifungal and antibacterial bioactivity. We showed that the resulting quintuple mutant can express foreign BGCs by heterologously producing actinorhodin, cinnamycin and prunustatin. We envisage that our strain will be a useful addition to the growing suite of heterologous expression hosts available for exploring microbial secondary metabolism.

scholarly journals A chromatogram-simplified Streptomyces albus host for heterologous production of natural products

2019 ◽  
Vol 113 (4) ◽  
pp. 511-520 ◽  
Author(s):  
Asif Fazal ◽  
Divya Thankachan ◽  
Ellie Harris ◽  
Ryan F. Seipke
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Gene Clusters ◽  
Heterologous Production ◽  
Biosynthetic Gene ◽  
Critical Aspect ◽  
Biosynthetic Gene Clusters ◽  
Streptomyces Albus ◽  
Microbial Natural Products ◽  
Suitable Expression

AbstractCloning natural product biosynthetic gene clusters from cultured or uncultured sources and their subsequent expression by genetically tractable heterologous hosts is an essential strategy for the elucidation and characterisation of novel microbial natural products. The availability of suitable expression hosts is a critical aspect of this workflow. In this work, we mutagenised five endogenous biosynthetic gene clusters from Streptomyces albus S4, which reduced the complexity of chemical extracts generated from the strain and eliminated antifungal and antibacterial bioactivity. We showed that the resulting quintuple mutant can express foreign biosynthetic gene clusters by heterologously producing actinorhodin, cinnamycin and prunustatin. We envisage that our strain will be a useful addition to the growing suite of heterologous expression hosts available for exploring microbial secondary metabolism.

A Natural Product Chemist's Guide to Unlocking Silent Biosynthetic Gene Clusters

2021 ◽  
Vol 90 (1) ◽  
Author(s):  
Brett C. Covington ◽  
Fei Xu ◽  
Mohammad R. Seyedsayamdost
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Gene Clusters ◽  
Annual Review ◽  
Publication Date ◽  
Biosynthetic Gene ◽  
Biosynthetic Gene Clusters ◽  
Research And Innovation ◽  
Therapeutic Leads ◽  
Microbial Natural Products

Microbial natural products have provided an important source of therapeutic leads and motivated research and innovation in diverse scientific disciplines. In recent years, it has become evident that bacteria harbor a large, hidden reservoir of potential natural products in the form of silent or cryptic biosynthetic gene clusters (BGCs). These can be readily identified in microbial genome sequences but do not give rise to detectable levels of a natural product. Herein, we provide a useful organizational framework for the various methods that have been implemented for interrogating silent BGCs. We divide all available approaches into four categories. The first three are endogenous strategies that utilize the native host in conjunction with classical genetics, chemical genetics, or different culture modalities. The last category comprises expression of the entire BGC in a heterologous host. For each category, we describe the rationale, recent applications, and associated advantages and limitations. Expected final online publication date for the Annual Review of Biochemistry, Volume 90 is June 2021. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.

scholarly journals Genetic platforms for heterologous expression of microbial natural products

2019 ◽  
Vol 36 (9) ◽  
pp. 1313-1332 ◽  
Author(s):  
Jia Jia Zhang ◽  
Xiaoyu Tang ◽  
Bradley S. Moore
Keyword(s):  
Natural Products ◽  
Heterologous Expression ◽  
Natural Product ◽  
Gene Clusters ◽  
Biosynthetic Gene ◽  
Biosynthetic Gene Clusters ◽  
Genetic Technologies ◽  
Microbial Natural Products

This review covers current genetic technologies for accessing and manipulating natural product biosynthetic gene clusters through heterologous expression.

scholarly journals Structure and biosynthesis of deoxy-polyamine in X. bovienii

2021 ◽  
Author(s):  
Sebastian L Wenski ◽  
Natalie Berghaus ◽  
Nadine Keller ◽  
Helge B Bode
Keyword(s):  
Natural Products ◽  
Gene Clusters ◽  
Mass Spectrometric ◽  
Spectrometric Analysis ◽  
Heterologous Production ◽  
Biosynthetic Gene ◽  
Biosynthetic Gene Clusters ◽  
In Trans ◽  
In Cis ◽  
Dh Domain

Abstract Polyamine moieties have been described as part of the fabclavine and zeamine family of natural products. While the corresponding biosynthetic gene clusters have been found in many different proteobacteria, a unique BGC was identified in the entomopathogenic bacterium Xenorhabdus bovienii. Mass spectrometric analysis of a X. bovienii mutant strain revealed a new deoxy-polyamine. The corresponding biosynthesis includes two additional reductive steps, initiated by an additional dehydratase (DH) domain, which was not found in any other Xenorhabdus strain. Moreover, this DH domain could be successfully integrated into homologous biosynthesis pathways, leading to the formation of other deoxy-polyamines. Additional heterologous production experiments revealed that the DH domain could act in cis as well as in trans.

scholarly journals Discovery and characterisation of an amidine-containing ribosomally-synthesised peptide that is widely distributed in nature

2020 ◽  
Author(s):  
Alicia H. Russell ◽  
Natalia M. Vior ◽  
Edward S. Hems ◽  
Rodney Lacret ◽  
Andrew W. Truman
Keyword(s):  
Natural Product ◽  
Genome Mining ◽  
Gene Clusters ◽  
Model Organisms ◽  
Biosynthetic Gene ◽  
Biosynthetic Gene Clusters ◽  
Post Translational Modifications ◽  
Streptomyces Albus ◽  
Modified Peptides ◽  
Mining Tool

ABSTRACTRibosomally synthesised and post-translationally modified peptides (RiPPs) are a structurally diverse class of natural product with a range of bioactivities. Genome mining for RiPP biosynthetic gene clusters (BGCs) is often hampered by poor detection of the short precursor peptides that are ultimately modified into the final molecule. Here, we utilise a previously described genome mining tool, RiPPER, to identify novel RiPP precursor peptides near YcaO-domain proteins, enzymes that catalyse various RiPP post-translational modifications including heterocyclisation and thioamidation. Using this dataset, we identified a novel, diverse and highly conserved family of RiPP BGCs spanning over 230 species of Actinobacteria and Firmicutes. A representative BGC from Streptomyces albus J1074 was characterised, leading to the discovery of streptamidine, a novel-amidine containing RiPP. This highlights the breadth of unexplored natural products with structurally rare features, even in model organisms.

scholarly journals Mining metagenomes for natural product biosynthetic gene clusters: unlocking new potential with ultrafast techniques

2021 ◽  
Author(s):  
Emiliano Pereira-Flores ◽  
Marnix Medema ◽  
Pier Luigi Buttigieg ◽  
Peter Meinicke ◽  
Frank Oliver Glöckner ◽  
...  
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Human Microbiome ◽  
Gene Clusters ◽  
Human Microbiome Project ◽  
Biosynthetic Gene Cluster ◽  
Metagenomic Data ◽  
Biosynthetic Gene ◽  
Biosynthetic Gene Clusters ◽  
Wide Range

Microorganisms produce an immense variety of natural products through the expression of Biosynthetic Gene Clusters (BGCs): physically clustered genes that encode the enzymes of a specialized metabolic pathway. These natural products cover a wide range of chemical classes (e.g., aminoglycosides, lantibiotics, nonribosomal peptides, oligosaccharides, polyketides, terpenes) that are highly valuable for industrial and medical applications1. Metagenomics, as a culture-independent approach, has greatly enhanced our ability to survey the functional potential of microorganisms and is growing in popularity for the mining of BGCs. However, to effectively exploit metagenomic data to this end, it will be crucial to more efficiently identify these genomic elements in highly complex and ever-increasing volumes of data2. Here, we address this challenge by developing the ultrafast Biosynthetic Gene cluster MEtagenomic eXploration toolbox (BiG-MEx). BiG-MEx rapidly identifies a broad range of BGC protein domains, assess their diversity and novelty, and predicts the abundance profile of natural product BGC classes in metagenomic data. We show the advantages of BiG-MEx compared to standard BGC-mining approaches, and use it to explore the BGC domain and class composition of samples in the TARA Oceans3 and Human Microbiome Project datasets4. In these analyses, we demonstrate BiG-MEx’s applicability to study the distribution, diversity, and ecological roles of BGCs in metagenomic data, and guide the exploration of natural products with clinical applications.

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