The DOI matches its Crossref record; 96 of the 96 references it cites were found in a registry or an index.
Recent advances in understanding Streptomyces
Open accessAbstract
About 2,500 papers dated 2014–2016 were recovered by searching the PubMed database for Streptomyces, which are the richest known source of antibiotics. This review integrates around 100 of these papers in sections dealing with evolution, ecology, pathogenicity, growth and development, stress responses and secondary metabolism, gene expression, and technical advances. Genomic approaches have greatly accelerated progress. For example, it has been definitively shown that interspecies recombination of conserved genes has occurred during evolution, in addition to exchanges of some of the tens of thousands of non-conserved accessory genes. The closeness of the association of Streptomyces with plants, fungi, and insects has become clear and is reflected in the importance of regulators of cellulose and chitin utilisation in overall Streptomyces biology. Interestingly, endogenous cellulose-like glycans are also proving important in hyphal growth and in the clumping that affects industrial fermentations. Nucleotide secondary messengers, including cyclic di-GMP, have been shown to provide key input into developmental processes such as germination and reproductive growth, while late morphological changes during sporulation involve control by phosphorylation. The discovery that nitric oxide is produced endogenously puts a new face on speculative models in which regulatory Wbl proteins (peculiar to actinobacteria) respond to nitric oxide produced in stressful physiological transitions. Some dramatic insights have come from a new model system for Streptomyces developmental biology, Streptomyces venezuelae, including molecular evidence of very close interplay in each of two pairs of regulatory proteins. An extra dimension has been added to the many complexities of the regulation of secondary metabolism by findings of regulatory crosstalk within and between pathways, and even between species, mediated by end products. Among many outcomes from the application of chromosome immunoprecipitation sequencing (ChIP-seq) analysis and other methods based on “next-generation sequencing” has been the finding that 21% of Streptomyces mRNA species lack leader sequences and conventional ribosome binding sites. Further technical advances now emerging should lead to continued acceleration of knowledge, and more effective exploitation, of these astonishing and critically important organisms.
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Cites
The nitrate-nitrite-nitric oxide pathway in physiology and therapeutics
Lundberg, J. O., Weitzberg, E., & Gladwin, M. T. (2008) · Nature Reviews Drug Discovery · doi:10.1038/nrd2466 · Cited by 2,739
Taxonomy, Physiology, and Natural Products of Actinobacteria
Barka, E. A., Vatsa, P., Sanchez, L., Gaveau-Vaillant, N., Jacquard, C., Klenk, H.-P., Clément, C., Ouhdouch, Y., & van Wezel, G. P. (2016) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00019-15 · Cited by 2,188
antiSMASH 3.0—a comprehensive resource for the genome mining of biosynthetic gene clusters
Weber, T., Blin, K., Duddela, S., Krug, D., Kim, H. U., Bruccoleri, R., Lee, S. Y., Fischbach, M. A., Müller, R., Wohlleben, W., et al. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv437 · Cited by 1,868
Molecular Regulation of Antibiotic Biosynthesis in Streptomyces
Liu, G., Chater, K. F., Chandra, G., Niu, G., & Tan, H. (2013) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00054-12 · Cited by 714
Self-citationThe complex extracellular biology of Streptomyces
Chater, K. F., Biró, S., Lee, K. J., Palmer, T., & Schrempf, H. (2010) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2009.00206.x · Cited by 495
Self-citationBertrand, S., Bohni, N., Schnee, S., Schumpp, O., Gindro, K., & Wolfender, J.-L. (2014) · Biotechnology Advances · doi:10.1016/j.biotechadv.2014.03.001 · Cited by 487
CRISPR-Cas9 Based Engineering of Actinomycetal Genomes
Tong, Y., Charusanti, P., Zhang, L., Weber, T., & Lee, S. Y. (2015) · ACS Synthetic Biology · doi:10.1021/acssynbio.5b00038 · Cited by 432
Streptomyces as symbionts: an emerging and widespread theme?
Seipke, R. F., Kaltenpoth, M., & Hutchings, M. I. (2012) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2011.00313.x · Cited by 417
Streptomyces as a plant's best friend?
Viaene, T., Langendries, S., Beirinckx, S., Maes, M., & Goormachtig, S. (2016) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiw119 · Cited by 374
One-step high-efficiency CRISPR/Cas9-mediated genome editing in Streptomyces
Huang, H., Zheng, G., Jiang, W., Hu, H., & Lu, Y. (2015) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmv007 · Cited by 289
Cited by
Stan, D., Enciu, A.-M., Mateescu, A. L., Ion, A. C., Brezeanu, A. C., Stan, D., & Tanase, C. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.723233 · Cited by 269
Metadata
- Authors
- Chater, K. F.
- Venue
- F1000Research
- Publisher
- F1000 Research Ltd
- Published
- 2016-11-30
- Volume
- 5
- Pages
- 2795
- ISSN
- 2046-1402 (ISSN-L)
- OpenAlex
- W2558649940
- Cited by
- 266
- References
- 96
- FWCI
- 13.16
- Type
- journal article
- Language
- en
- Open access
- gold
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.