High production of a class III lantipeptide AmfS in Streptomyces griseus

References

• Katz L, Baltz RH. Natural product discovery: past, present, and future. J. Ind. Microbiol. Biotechnol. 2016;43:155–176.10.1007/s10295-015-1723-5
   PubMed Web of Science ®Google Scholar
• Barka EA, Vatsa P, Sanchez L, et al. Taxonomy, physiology, and natural products of Actinobacteria. Microbiol. Mol. Biol. Rev. 2016;80:1–43.10.1128/MMBR.00019-15
   PubMed Web of Science ®Google Scholar
• Flärdh K, Buttner MJ. Streptomyces morphogenetics: dissecting differentiation in a filamentous bacterium. Nat. Rev. Microbiol. 2009;7:36–49.10.1038/nrmicro1968
   PubMed Web of Science ®Google Scholar
• Ikeda H, Shin-ya K, Omura S. Genome mining of the Streptomyces avermitilis genome and development of genome-minimized hosts for heterologous expression of biosynthetic gene clusters. J. Ind. Microbiol. Biotechnol. 2014;41:233–250.10.1007/s10295-013-1327-x
   PubMed Web of Science ®Google Scholar
• Ikeda H, Ishikawa J, Hanamoto A, et al. Complete genome sequence and comparative analysis of the industrial microorganism Streptomyces avermitilis. Nat. Biotechnol. 2003;21:526–531.10.1038/nbt820
   PubMed Web of Science ®Google Scholar
• Arnison PG, Bibb MJ, Bierbaum G, et al. Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature. Nat. Prod. Rep. 2013;30:108–160.10.1039/C2NP20085F
   PubMed Web of Science ®Google Scholar
• Lubelski J, Rink R, Khusainov R, et al. Biosynthesis, immunity, regulation, mode of action and engineering of the model lantibiotic nisin. Cell. Mol. Life Sci. 2008;65:455–476.10.1007/s00018-007-7171-2
   PubMed Web of Science ®Google Scholar
• Willey JM, van der Donk WA. Lantibiotics: peptides of diverse structure and function. Annu. Rev. Microbiol. 2007;61:477–501.10.1146/annurev.micro.61.080706.093501
   PubMed Web of Science ®Google Scholar
• Willey JM, Gaskell AA. Morphogenetic signaling molecules of the streptomycetes. Chem. Rev. 2011;111:174–187.10.1021/cr1000404
   PubMed Web of Science ®Google Scholar
• Iorio M, Sasso O, Maffioli SI, et al. A glycosylated, labionin-containing lanthipeptide with marked antinociceptive activity. ACS Chem. Biol. 2014;9:398–404.10.1021/cb400692w
   PubMed Web of Science ®Google Scholar
• Férir G, Petrova MI, Andrei G, et al. The lantibiotic peptide labyrinthopeptin A1 demonstrates broad anti-HIV and anti-HSV activity with potential for microbicidal applications. PLoS ONE. 2013;8:e64010.10.1371/journal.pone.0064010
   PubMed Web of Science ®Google Scholar
• Kodani S, Lodato MA, Durrant MC, et al. SapT, a lanthionine-containing peptide involved in aerial hyphae formation in the streptomycetes. Mol. Microbiol. 2005;58:1368–1380.10.1111/j.1365-2958.2005.04921.x
   PubMed Web of Science ®Google Scholar
• Ueda K, Takano H, Nishimoto M, et al. Dual transcriptional control of amfTSBA, which regulates the onset of cellular differentiation in Streptomyces griseus. J. Bacteriol. 2005;187:135–142.10.1128/JB.187.1.135-142.2005
   PubMed Web of Science ®Google Scholar
• Ueda K, Oinuma K, Ikeda G, et al. AmfS, an extracellular peptidic morphogen in Streptomyces griseus. J. Bacteriol. 2002;184:1488–1492.10.1128/JB.184.5.1488-1492.2002
   PubMed Web of Science ®Google Scholar
• Keijser BJ, van Wezel GP, Canters GW, et al. Developmental regulation of the Streptomyces lividans ram genes: involvement of RamR in regulation of the ramCSAB operon. J. Bacteriol. 2002;184:4420–4429.10.1128/JB.184.16.4420-4429.2002
   PubMed Web of Science ®Google Scholar
• Nguyen KT, Willey JM, Nguyen LD, et al. A central regulator of morphological differentiation in the multicellular bacterium Streptomyces coelicolor. Mol. Microbiol. 2002;46:1223–1238.10.1046/j.1365-2958.2002.03255.x
   PubMed Web of Science ®Google Scholar
• Bentley SD, Chater KF, Cerdeño-Tárraga AM, et al. Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2). Nature. 2002;417:141–147.10.1038/417141a
   PubMed Web of Science ®Google Scholar
• Yamazaki H, Takano Y, Ohnishi Y, et al. amfR, an essential gene for aerial mycelium formation, is a member of the AdpA regulon in the A-factor regulatory cascade in Streptomyces griseus. Mol. Microbiol. 2003;50:1173–1187.10.1046/j.1365-2958.2003.03760.x
   PubMed Web of Science ®Google Scholar
• Ochi K, Hosaka T. New strategies for drug discovery: activation of silent or weakly expressed microbial gene clusters. Appl. Microbiol. Biotechnol. 2013;97:87–98.10.1007/s00253-012-4551-9
   PubMed Web of Science ®Google Scholar
• Amano SI, Sakurai T, Endo K, et al. A cryptic antibiotic triggered by monensin. J. Antibiot. (Tokyo). 2011;64:703p.10.1038/ja.2011.69
   PubMed Web of Science ®Google Scholar
• Yoon V, Nodwell JR. Activating secondary metabolism with stress and chemicals. J. Ind. Microbiol. Biotechnol. 2014;41:415–424.10.1007/s10295-013-1387-y
   PubMed Web of Science ®Google Scholar
• Onaka H, Tabata H, Igarashi Y, et al. Goadsporin, a chemical substance which promotes secondary metabolism and morphogenesis in streptomycetes. I. Purification and characterization. J. Antibiot. (Tokyo). 2001;54:1036–1044.10.7164/antibiotics.54.1036
   PubMed Web of Science ®Google Scholar
• Komatsu M, Uchiyama T, Omura S, et al. Genome-minimized Streptomyces host for the heterologous expression of secondary metabolism. Proc. Natl. Acad. Sci. U S A. 2010;107:2646–2651.10.1073/pnas.0914833107
   PubMed Web of Science ®Google Scholar
• Gomez-Escribano JP, Bibb MJ. Heterologous expression of natural product biosynthetic gene clusters in Streptomyces coelicolor: from genome mining to manipulation of biosynthetic pathways. J. Ind. Microbiol. Biotechnol. 2014;41:425–431.10.1007/s10295-013-1348-5
   PubMed Web of Science ®Google Scholar
• Komatsu M, Komatsu K, Koiwai H, et al. Engineered streptomyces avermitilis host for heterologous expression of biosynthetic gene cluster for secondary metabolites. ACS Synth. Biol. 2013;2:384–396.10.1021/sb3001003
   PubMed Web of Science ®Google Scholar
• Du D, Katsuyama Y, Onaka H, et al. Production of a novel amide-containing polyene by activating a cryptic biosynthetic gene cluster in Streptomyces sp. Chembiochem. 2016;17:1464–1471.
   PubMed Web of Science ®Google Scholar
• Laureti L, Song L, Huang S, et al. Identification of a bioactive 51-membered macrolide complex by activation of a silent polyketide synthase in Streptomyces ambofaciens. Proc. Natl. Acad. Sci. U S A. 2011;108:6258–6263.10.1073/pnas.1019077108
   PubMed Web of Science ®Google Scholar
• Onaka H, Mori Y, Igarashi Y, et al. Mycolic acid-containing bacteria induce natural-product biosynthesis in streptomyces species. Appl. Environ. Microbiol. 2011;77:400–406.10.1128/AEM.01337-10
   PubMed Web of Science ®Google Scholar
• Völler GH, Krawczyk JM, Pesic A, et al. Characterization of new class III lantibiotics-erythreapeptin, avermipeptin and griseopeptin from Saccharopolyspora erythraea, Streptomyces avermitilis and Streptomyces griseus demonstrates stepwise N-terminal leader processing. Chembiochem. 2012;13:1174–1183.10.1002/cbic.v13.8
   PubMed Web of Science ®Google Scholar
• Komatsu M, Tsuda M, Omura S, et al. Identification and functional analysis of genes controlling biosynthesis of 2-methylisoborneol. Proc. Natl. Acad. Sci. U S A. 2008;105:7422–7427.10.1073/pnas.0802312105
   PubMed Web of Science ®Google Scholar
• Gusek TW, Kinsella JE. Review of the Streptomyces lividans/vector pIJ702 system for gene cloning. Crit. Rev. Microbiol. 1992;18:247–260.10.3109/10408419209113517
   PubMed Web of Science ®Google Scholar
• Sun J, Kelemen GH, Fernández-Abalos JM, et al. Green fluorescent protein as a reporter for spatial and temporal gene expression in Streptomyces coelicolor A3(2). Microbiology. 1999;145(Pt 9):2221–2227.10.1099/00221287-145-9-2221
   PubMed Web of Science ®Google Scholar
• Ueda K, Miyake K, Horinouchi S, et al. A gene cluster involved in aerial mycelium formation in Streptomyces griseus encodes proteins similar to the response regulators of two-component regulatory systems and membrane translocators. J. Bacteriol. 1993;175:2006–2016.
   PubMed Web of Science ®Google Scholar
• Kieser T, Bibb MJ, Buttner MJ, et al. Practical Streptomyces genetics. Norwich: The John Innes Foundation; 2000.
   Google Scholar
• Maniatis T, Fritsch EF, Sambrook J. Molecular cloning: a laboratory manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 1982.
   Google Scholar
• Schägger H, von Jagow G. Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa. Anal. Biochem. 1987;166:368–379.10.1016/0003-2697(87)90587-2
   PubMed Web of Science ®Google Scholar
• Willey JM, Willems A, Kodani S, et al. Morphogenetic surfactants and their role in the formation of aerial hyphae in Streptomyces coelicolor. Mol. Microbiol. 2006;59:731–742.10.1111/mmi.2006.59.issue-3
   PubMed Web of Science ®Google Scholar
• Kodani S, Hudson ME, Durrant MC, et al. The SapB morphogen is a lantibiotic-like peptide derived from the product of the developmental gene ramS in Streptomyces coelicolor. Proc. Natl. Acad. Sci. U S A. 2004;101:11448–11453.10.1073/pnas.0404220101
   PubMed Web of Science ®Google Scholar
• Horinouchi S, Beppu T. Hormonal control by A-factor of morphological development and secondary metabolism in Streptomyces. Proc. Jpn. Acad. Ser. B Phys. Biol. Sci. 2007;83:277–295.10.2183/pjab.83.277
   PubMed Web of Science ®Google Scholar
• Gubbens J, Janus M, Florea BI, et al. Identification of glucose kinase-dependent and -independent pathways for carbon control of primary metabolism, development and antibiotic production in Streptomyces coelicolor by quantitative proteomics. Mol. Microbiol. 2012;86:1490–1507.10.1111/mmi.2012.86.issue-6
   PubMed Web of Science ®Google Scholar