Skip to main content
Log in

Genome mining of Streptomyces ambofaciens

  • Mini-Review
  • Published:
Journal of Industrial Microbiology & Biotechnology

Abstract

Since the discovery of the streptomycin produced by Streptomyces griseus in the middle of the last century, members of this bacterial genus have been largely exploited for the production of secondary metabolites with wide uses in medicine and in agriculture. They have even been recognized as one of the most prolific producers of natural products among microorganisms. With the onset of the genomic era, it became evident that these microorganisms still represent a major source for the discovery of novel secondary metabolites. This was highlighted with the complete genome sequencing of Streptomyces coelicolor A3(2) which revealed an unexpected potential of this organism to synthesize natural products undetected until then by classical screening methods. Since then, analysis of sequenced genomes from numerous Streptomyces species has shown that a single species can carry more than 30 secondary metabolite gene clusters, reinforcing the idea that the biosynthetic potential of this bacterial genus is far from being fully exploited. This review highlights our knowledge on the potential of Streptomyces ambofaciens ATCC 23877 to synthesize natural products. This industrial strain was known for decades to only produce the drug spiramycin and another antibacterial compound, congocidine. Mining of its genome allowed the identification of 23 clusters potentially involved in the production of other secondary metabolites. Studies of some of these clusters resulted in the characterization of novel compounds and of previously known compounds but never characterized in this Streptomyces species. In addition, genome mining revealed that secondary metabolite gene clusters of phylogenetically closely related Streptomyces are mainly species-specific.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Aigle B, Bunet R, Corre C, Garénaux A, Hotel L, Huang S, Laureti L, Lautru S, Mendes MV, Nezbedova S, Nguyen HC, Song L, Weiser J, Challis G, Leblond P, Pernodet JL (2011) Genome-guided exploration of Streptomyces ambofaciens secondary metabolism. In: Dyson P (ed) Streptomyces, molecular biology and biotechnology. Caister Academic, Norfolk, pp 179–194

  2. Aigle B, Corre C (2012) Waking up Streptomyces secondary metabolism by constitutive expression of activators or genetic disruption of repressors. Methods Enzymol 517:343–366. doi:10.1016/B978-0-12-404634-4.00017-6

    CAS  PubMed  Google Scholar 

  3. Aigle B, Pang X, Decaris B, Leblond P (2005) Involvement of AlpV, a new member of the Streptomyces antibiotic regulatory protein family, in regulation of the duplicated type II polyketide synthase alp gene cluster in Streptomyces ambofaciens. J Bacteriol 187(7):2491–2500. doi:10.1128/JB.187.7.2491-2500.2005

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  4. Baltz R (2007) Antimicrobials from actinomycetes: back to the future. Microbe 2(3):125–131

    Google Scholar 

  5. Barona-Gomez F, Lautru S, Francou FX, Leblond P, Pernodet JL, Challis GL (2006) Multiple biosynthetic and uptake systems mediate siderophore-dependent iron acquisition in Streptomyces coelicolor A3(2) and Streptomyces ambofaciens ATCC 23877. Microbiology 152(Pt 11):3355–3366. doi:10.1099/mic.0.29161-0

    Article  CAS  PubMed  Google Scholar 

  6. Barona-Gomez F, Wong U, Giannakopulos AE, Derrick PJ, Challis GL (2004) Identification of a cluster of genes that directs desferrioxamine biosynthesis in Streptomyces coelicolor M145. J Am Chem Soc 126(50):16282–16283. doi:10.1021/ja045774k

    Article  CAS  PubMed  Google Scholar 

  7. Bentley SD, Chater KF, Cerdeno-Tarraga AM, Challis GL, Thomson NR, James KD, Harris DE, Quail MA, Kieser H, Harper D, Bateman A, Brown S, Chandra G, Chen CW, Collins M, Cronin A, Fraser A, Goble A, Hidalgo J, Hornsby T, Howarth S, Huang CH, Kieser T, Larke L, Murphy L, Oliver K, O’Neil S, Rabbinowitsch E, Rajandream MA, Rutherford K, Rutter S, Seeger K, Saunders D, Sharp S, Squares R, Squares S, Taylor K, Warren T, Wietzorrek A, Woodward J, Barrell BG, Parkhill J, Hopwood DA (2002) Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2). Nature 417(6885):141–147. doi:10.1038/417141a

    Article  PubMed  Google Scholar 

  8. Bergmann S, Schumann J, Scherlach K, Lange C, Brakhage AA, Hertweck C (2007) Genomics-driven discovery of PKS-NRPS hybrid metabolites from Aspergillus nidulans. Nat Chem Biol 3(4):213–217. doi:10.1038/nchembio869

    Article  CAS  PubMed  Google Scholar 

  9. Bisang C, Long PF, Cortes J, Westcott J, Crosby J, Matharu AL, Cox RJ, Simpson TJ, Staunton J, Leadlay PF (1999) A chain initiation factor common to both modular and aromatic polyketide synthases. Nature 401(6752):502–505. doi:10.1038/46829

    Article  CAS  PubMed  Google Scholar 

  10. Bunet R, Mendes MV, Rouhier N, Pang X, Hotel L, Leblond P, Aigle B (2008) Regulation of the synthesis of the angucyclinone antibiotic alpomycin in Streptomyces ambofaciens by the autoregulator receptor AlpZ and its specific ligand. J Bacteriol 190(9):3293–3305. doi:10.1128/JB.01989-07

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  11. Bunet R, Song L, Mendes MV, Corre C, Hotel L, Rouhier N, Framboisier X, Leblond P, Challis GL, Aigle B (2011) Characterization and manipulation of the pathway-specific late regulator AlpW reveals Streptomyces ambofaciens as a new producer of kinamycins. J Bacteriol 193(5):1142–1153. doi:10.1128/JB.01269-10

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  12. Chew WK, Segarra I, Ambu S, Mak JW (2012) Significant reduction of brain cysts caused by Toxoplasma gondii after treatment with spiramycin coadministered with metronidazole in a mouse model of chronic toxoplasmosis. Antimicrob Agents Chemother 56(4):1762–1768. doi:10.1128/AAC.05183-11

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  13. Choulet F, Aigle B, Gallois A, Mangenot S, Gerbaud C, Truong C, Francou FX, Fourrier C, Guerineau M, Decaris B, Barbe V, Pernodet JL, Leblond P (2006) Evolution of the terminal regions of the Streptomyces linear chromosome. Mol Biol Evol 23(12):2361–2369. doi:10.1093/molbev/msl108

    Article  CAS  PubMed  Google Scholar 

  14. Citron CA, Gleitzmann J, Laurenzano G, Pukall R, Dickschat JS (2012) Terpenoids are widespread in actinomycetes: a correlation of secondary metabolism and genome data. ChemBioChem 13(2):202–214. doi:10.1002/cbic.201100641

    Article  CAS  PubMed  Google Scholar 

  15. Cosar C, Ninet L, Pinnert-Sindico S, Preud’Homme J (1952) Trypanocide action of an antibiotic produced by a Streptomyces. C R Hebd Seances Acad Sci 234(14):1498–1499

    CAS  PubMed  Google Scholar 

  16. Finlay AC, Hochstein FA, Sobin BA, Murphy FX (1951) Netropsin, a new antibiotic produced by a Streptomyces. J Am Chem Soc 73:341–343

    Article  CAS  Google Scholar 

  17. Geistlich M, Losick R, Turner JR, Rao RN (1992) Characterization of a novel regulatory gene governing the expression of a polyketide synthase gene in Streptomyces ambofaciens. Mol Microbiol 6(14):2019–2029

    Article  CAS  PubMed  Google Scholar 

  18. Gerber N (1973) Volatile lactones from Streptomyces. Tetrahedron Lett 14(10):771–774

    Article  Google Scholar 

  19. Gokhale RS, Hunziker D, Cane DE, Khosla C (1999) Mechanism and specificity of the terminal thioesterase domain from the erythromycin polyketide synthase. Chem Biol 6(2):117–125. doi:10.1016/S1074-5521(99)80008-8

    Article  CAS  PubMed  Google Scholar 

  20. Gomez-Escrabino J, Song L, Fox D, Yeo V, Bibb M, Challis G (2012) Structure and biosynthesis of the unusual polyketide alkaloid coelimycin P1, a metabolic product of the cpk gene cluster of Streptomyces coelicolor M145. Chem Sci 3:2716–2720

    Article  Google Scholar 

  21. Gomez-Escribano JP, Bibb MJ (2012) Streptomyces coelicolor as an expression host for heterologous gene clusters. Methods Enzymol 517:279–300. doi:10.1016/B978-0-12-404634-4.00014-0

    CAS  PubMed  Google Scholar 

  22. Gomez-Escribano JP, Bibb MJ (2013) Heterologous expression of natural product biosynthetic gene clusters in Streptomyces coelicolor: from genome mining to manipulation of biosynthetic pathways. J Ind Microbiol Biotechnol. doi:10.1007/s10295-013-1348-5

    PubMed  Google Scholar 

  23. Gould SJ (1997) Biosynthesis of the kinamycins. Chem Rev 97(7):2499–2510

    Article  CAS  PubMed  Google Scholar 

  24. Gould SJ, Hong ST, Carney JR (1998) Cloning and heterologous expression of genes from the kinamycin biosynthetic pathway of Streptomyces murayamaensis. J Antibiot (Tokyo) 51(1):50–57

    Article  CAS  Google Scholar 

  25. Hasinoff BB, Wu X, Yalowich JC, Goodfellow V, Laufer RS, Adedayo O, Dmitrienko GI (2006) Kinamycins A and C, bacterial metabolites that contain an unusual diazo group, as potential new anticancer agents: antiproliferative and cell cycle effects. Anticancer Drugs 17(7):825–837

    Article  CAS  PubMed  Google Scholar 

  26. Juguet M, Lautru S, Francou FX, Nezbedova S, Leblond P, Gondry M, Pernodet JL (2009) An iterative nonribosomal peptide synthetase assembles the pyrrole-amide antibiotic congocidine in Streptomyces ambofaciens. Chem Biol 16(4):421–431. doi:10.1016/j.chembiol.2009.03.010

    Article  CAS  PubMed  Google Scholar 

  27. Kaiser S, Muller JJ, Froehlich PE, Baggio Gnoatto SC, Bergold AM (2013) From bacteria to antineoplastic: epothilones a successful history. Anticancer Agents Med Chem 13(7):1057–1068

    Article  CAS  PubMed  Google Scholar 

  28. Kamra P, Gokhale RS, Mohanty D (2005) SEARCHGTr: a program for analysis of glycosyltransferases involved in glycosylation of secondary metabolites. Nucleic Acids Res 33 (Web Server issue):W220–W225. doi:10.1093/nar/gki449

  29. Karray F, Darbon E, Nguyen HC, Gagnat J, Pernodet JL (2010) Regulation of the biosynthesis of the macrolide antibiotic spiramycin in Streptomyces ambofaciens. J Bacteriol 192(21):5813–5821. doi:10.1128/JB.00712-10

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  30. Karray F, Darbon E, Oestreicher N, Dominguez H, Tuphile K, Gagnat J, Blondelet-Rouault MH, Gerbaud C, Pernodet JL (2007) Organization of the biosynthetic gene cluster for the macrolide antibiotic spiramycin in Streptomyces ambofaciens. Microbiology 153(Pt 12):4111–4122. doi:10.1099/mic.0.2007/009746-0

    Article  CAS  PubMed  Google Scholar 

  31. Keatinge-Clay AT (2007) A tylosin ketoreductase reveals how chirality is determined in polyketides. Chem Biol 14(8):898–908. doi:10.1016/j.chembiol.2007.07.009

    Article  CAS  PubMed  Google Scholar 

  32. Kelly WL, Pan L, Li C (2009) Thiostrepton biosynthesis: prototype for a new family of bacteriocins. J Am Chem Soc 131(12):4327–4334. doi:10.1021/ja807890a

    Article  CAS  PubMed  Google Scholar 

  33. Kim BS, Cropp TA, Beck BJ, Sherman DH, Reynolds KA (2002) Biochemical evidence for an editing role of thioesterase II in the biosynthesis of the polyketide pikromycin. J Biol Chem 277(50):48028–48034. doi:10.1074/jbc.M207770200

    Article  CAS  PubMed  Google Scholar 

  34. Kuhstoss S, Huber M, Turner JR, Paschal JW, Rao RN (1996) Production of a novel polyketide through the construction of a hybrid polyketide synthase. Gene 183(1–2):231–236

    Article  CAS  PubMed  Google Scholar 

  35. Kuscer E, Coates N, Challis I, Gregory M, Wilkinson B, Sheridan R, Petkovic H (2007) Roles of rapH and rapG in positive regulation of rapamycin biosynthesis in Streptomyces hygroscopicus. J Bacteriol 189(13):4756–4763. doi:10.1128/JB.00129-07

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  36. Kwan DH, Sun Y, Schulz F, Hong H, Popovic B, Sim-Stark JC, Haydock SF, Leadlay PF (2008) Prediction and manipulation of the stereochemistry of enoylreduction in modular polyketide synthases. Chem Biol 15(11):1231–1240. doi:10.1016/j.chembiol.2008.09.012

    Article  CAS  PubMed  Google Scholar 

  37. Laureti L, Song L, Huang S, Corre C, Leblond P, Challis GL, Aigle B (2011) 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 108(15):6258–6263. doi:10.1073/pnas.1019077108

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  38. Lautru S, Deeth RJ, Bailey LM, Challis GL (2005) Discovery of a new peptide natural product by Streptomyces coelicolor genome mining. Nat Chem Biol 1(5):265–269. doi:10.1038/nchembio731

    Article  CAS  PubMed  Google Scholar 

  39. Lautru S, Gondry M, Genet R, Pernodet JL (2002) The albonoursin gene cluster of S noursei biosynthesis of diketopiperazine metabolites independent of nonribosomal peptide synthetases. Chem Biol 9(12):1355–1364

    Article  CAS  PubMed  Google Scholar 

  40. Lautru S, Song L, Demange L, Lombes T, Galons H, Challis GL, Pernodet JL (2012) A sweet origin for the key congocidine precursor 4-acetamidopyrrole-2-carboxylate. Angew Chem Int Ed Engl 51(30):7454–7458. doi:10.1002/anie.201201445

    Article  CAS  PubMed  Google Scholar 

  41. Leben C, Keitt G (1948) An antibiotic substance active against certain phytopathogens. Phytopathology 38:899–906

    Google Scholar 

  42. Leblond P, Demuyter P, Simonet JM, Decaris B (1991) Genetic instability and associated genome plasticity in Streptomyces ambofaciens: pulsed-field gel electrophoresis evidence for large DNA alterations in a limited genomic region. J Bacteriol 173(13):4229–4233

    CAS  PubMed Central  PubMed  Google Scholar 

  43. Lee SJ, Kim EA, Song KS, Kim MJ, Lee DH, Kwon TK, Lee TJ (2012) Antimycin A sensitizes cells to TRAIL-induced apoptosis through upregulation of DR5 and downregulation of c-FLIP and Bcl-2. Int J Oncol 41(4):1425–1430. doi:10.3892/ijo2012.1575

    CAS  PubMed  Google Scholar 

  44. Li MH, Ung PM, Zajkowski J, Garneau-Tsodikova S, Sherman DH (2009) Automated genome mining for natural products. BMC Bioinformatics 10:185. doi:10.1186/1471-2105-10-185

    Article  PubMed Central  PubMed  Google Scholar 

  45. Medema MH, Blin K, Cimermancic P, de Jager V, Zakrzewski P, Fischbach MA, Weber T, Takano E, Breitling R (2011) antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences. Nucleic Acids Res 39 (Web Server issue):W339–W346. doi:10.1093/nar/gkr466

  46. Medema MH, Trefzer A, Kovalchuk A, van den Berg M, Muller U, Heijne W, Wu L, Alam MT, Ronning CM, Nierman WC, Bovenberg RA, Breitling R, Takano E (2010) The sequence of a 1.8-mb bacterial linear plasmid reveals a rich evolutionary reservoir of secondary metabolic pathways. Genome Biol Evol 2:212–224. doi:10.1093/gbe/evq013

    Article  PubMed Central  PubMed  Google Scholar 

  47. Mochizuki S, Hiratsu K, Suwa M, Ishii T, Sugino F, Yamada K, Kinashi H (2003) The large linear plasmid pSLA2-L of Streptomyces rochei has an unusually condensed gene organization for secondary metabolism. Mol Microbiol 48(6):1501–1510

    Article  CAS  PubMed  Google Scholar 

  48. Moore JM, Bradshaw E, Seipke RF, Hutchings MI, McArthur M (2012) Use and discovery of chemical elicitors that stimulate biosynthetic gene clusters in Streptomyces bacteria. Methods Enzymol 517:367–385. doi:10.1016/B978-0-12-404634-4.00018-8

    CAS  PubMed  Google Scholar 

  49. Nguyen HC, Darbon E, Thai R, Pernodet JL, Lautru S (2013) Post-PKS tailoring steps of the spiramycin macrolactone ring in Streptomyces ambofaciens. Antimicrob Agents Chemother 57(8):3836–3842. doi:10.1128/AAC.00512-13

    Article  CAS  PubMed  Google Scholar 

  50. Nguyen HC, Karray F, Lautru S, Gagnat J, Lebrihi A, Huynh TD, Pernodet JL (2010) Glycosylation steps during spiramycin biosynthesis in Streptomyces ambofaciens: involvement of three glycosyltransferases and their interplay with two auxiliary proteins. Antimicrob Agents Chemother 54(7):2830–2839. doi:10.1128/AAC.01602-09

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  51. O’Hara KA, Dmitrienko GI, Hasinoff BB (2010) Kinamycin F downregulates cyclin D3 in human leukemia K562 cells. Chem Biol Interact 184(3):396–402. doi:10.1016/j.cbi.2010.01.013

    Article  PubMed  Google Scholar 

  52. Ochi K, Hosaka T (2013) New strategies for drug discovery: activation of silent or weakly expressed microbial gene clusters. Appl Microbiol Biotechnol 97(1):87–98. doi:10.1007/s00253-012-4551-9

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  53. Ochi K, Tanaka Y, Tojo S (2013) Activating the expression of bacterial cryptic genes by rpoB mutations in RNA polymerase or by rare earth elements. J Ind Microbiol Biotechnol. doi:10.1007/s10295-013-1349-4

    PubMed  Google Scholar 

  54. Pang X, Aigle B, Girardet JM, Mangenot S, Pernodet JL, Decaris B, Leblond P (2004) Functional angucycline-like antibiotic gene cluster in the terminal inverted repeats of the Streptomyces ambofaciens linear chromosome. Antimicrob Agents Chemother 48(2):575–588

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  55. Parajuli N, Basnet DB, Chan Lee H, Sohng JK, Liou K (2004) Genome analyses of Streptomyces peucetius ATCC 27952 for the identification and comparison of cytochrome P450 complement with other Streptomyces. Arch Biochem Biophys 425(2):233–241. doi:10.1016/j.abb.2004.03.011

    Article  CAS  PubMed  Google Scholar 

  56. Pinnert-Sindico S (1954) Une nouvelle espèce de Streptomyces productrice d’antibiotiques: Streptomyces ambofaciens n. sp. caractères culturaux. Ann Inst Pasteur (Paris) 87(6):702–707

    CAS  Google Scholar 

  57. Poulet PP, Duffaut D, Barthet P, Brumpt I (2005) Concentrations and in vivo antibacterial activity of spiramycin and metronidazole in patients with periodontitis treated with high-dose metronidazole and the spiramycin/metronidazole combination. J Antimicrob Chemother 55(3):347–351. doi:10.1093/jac/dki013

    Article  CAS  PubMed  Google Scholar 

  58. Rebets Y, Brotz E, Tokovenko B, Luzhetskyy A (2013) Actinomycetes biosynthetic potential: how to bridge in silico and in vivo? J Ind Microbiol Biotechnol. doi:10.1007/s10295-013-1352-9

    PubMed  Google Scholar 

  59. Reid R, Piagentini M, Rodriguez E, Ashley G, Viswanathan N, Carney J, Santi DV, Hutchinson CR, McDaniel R (2003) A model of structure and catalysis for ketoreductase domains in modular polyketide synthases. Biochemistry 42(1):72–79. doi:10.1021/bi0268706

    Article  CAS  PubMed  Google Scholar 

  60. Richardson MA, Kuhstoss S, Huber ML, Ford L, Godfrey O, Turner JR, Rao RN (1990) Cloning of spiramycin biosynthetic genes and their use in constructing Streptomyces ambofaciens mutants defective in spiramycin biosynthesis. J Bacteriol 172(7):3790–3798

    CAS  PubMed Central  PubMed  Google Scholar 

  61. Richardson MA, Kuhstoss S, Solenberg P, Schaus NA, Rao RN (1987) A new shuttle cosmid vector, pKC505, for streptomycetes: its use in the cloning of three different spiramycin-resistance genes from a Streptomyces ambofaciens library. Gene 61(3):231–241

    Article  CAS  PubMed  Google Scholar 

  62. Riclea R, Aigle B, Leblond P, Schoenian I, Spiteller D, Dickschat JS (2012) Volatile lactones from streptomycetes arise via the antimycin biosynthetic pathway. ChemBioChem 13(11):1635–1644. doi:10.1002/cbic.201200260

    Article  CAS  PubMed  Google Scholar 

  63. Schoenian I, Paetz C, Dickschat JS, Aigle B, Leblond P, Spiteller D (2012) An unprecedented 1,2-shift in the biosynthesis of the 3-aminosalicylate moiety of antimycins. ChemBioChem 13(6):769–773. doi:10.1002/cbic.201200033

    Article  CAS  PubMed  Google Scholar 

  64. Seipke RF, Barke J, Brearley C, Hill L, Yu DW, Goss RJ, Hutchings MI (2011) A single Streptomyces symbiont makes multiple antifungals to support the fungus farming ant Acromyrmex octospinosus. PLoS ONE 6(8):e22028. doi:10.1371/journal.pone.0022028

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  65. Stumpp T, Himbert S, Altenbuchner J (2005) Cloning of the netropsin resistance genes from Streptomyces flavopersicus NRRL 2820. J Basic Microbiol 45(5):355–362. doi:10.1002/jobm.200410529

    Article  CAS  PubMed  Google Scholar 

  66. Tener G, Merlin Bumpus F, Dunshee B, Strong F (1953) The structure of antimycin A. II. Degradation studies. J Am Chem Soc 75(5):1100–1104

    Article  CAS  Google Scholar 

  67. Tener G, van Tamelen E, Strong F (1953) The chemistry of antimycin A. III. Structure of the antimycic acid. J Am Chem Soc 75(15):3623–3625

    Article  CAS  Google Scholar 

  68. van Tamelen E, Strong F, Quarck U (1959) The chemistry of antimycin A. IV. Study of the structure of antimycin lactone. J Am Chem Soc 81(3):750–751

    Article  Google Scholar 

  69. van Wezel GP, McDowall KJ (2011) The regulation of the secondary metabolism of Streptomyces: new links and experimental advances. Nat Prod Rep 28(7):1311–1333. doi:10.1039/c1np00003a

    Article  PubMed  Google Scholar 

  70. Welker M, Dittmann E, von Dohren H (2012) Cyanobacteria as a source of natural products. Methods Enzymol 517:23–46. doi:10.1016/B978-0-12-404634-4.00002-4

    CAS  PubMed  Google Scholar 

  71. Wilkinson CJ, Hughes-Thomas ZA, Martin CJ, Bohm I, Mironenko T, Deacon M, Wheatcroft M, Wirtz G, Staunton J, Leadlay PF (2002) Increasing the efficiency of heterologous promoters in actinomycetes. J Mol Microbiol Biotechnol 4(4):417–426

    CAS  PubMed  Google Scholar 

  72. Wilson DJ, Xue Y, Reynolds KA, Sherman DH (2001) Characterization and analysis of the PikD regulatory factor in the pikromycin biosynthetic pathway of Streptomyces venezuelae. J Bacteriol 183(11):3468–3475. doi:10.1128/JB.183.11.3468-3475.2001

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  73. Yadav G, Gokhale RS, Mohanty D (2003) Computational approach for prediction of domain organization and substrate specificity of modular polyketide synthases. J Mol Biol 328(2):335–363

    Article  CAS  PubMed  Google Scholar 

  74. Yadav G, Gokhale RS, Mohanty D (2003) SEARCHPKS: a program for detection and analysis of polyketide synthase domains. Nucleic Acids Res 31(13):3654–3658

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  75. Zhu H, Sandiford SK, van Wezel GP (2013) Triggers and cues that activate antibiotic production by actinomycetes. J Ind Microbiol Biotechnol. doi:10.1007/s10295-013-1309-z

    Google Scholar 

  76. Ziemert N, Podell S, Penn K, Badger JH, Allen E, Jensen PR (2012) The natural product domain seeker NaPDoS: a phylogeny based bioinformatic tool to classify secondary metabolite gene diversity. PLoS ONE 7(3):e34064. doi:10.1371/journal.pone.0034064

    Article  CAS  PubMed Central  PubMed  Google Scholar 

Download references

Acknowledgments

This work was supported by the European Community under the ActinoGEN 6th framework programme (FP6-5224), the French National Research Agency through the Laboratory of Excellence ARBRE (ANR-12- LABXARBRE-01) and the Région Lorraine.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Bertrand Aigle.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Aigle, B., Lautru, S., Spiteller, D. et al. Genome mining of Streptomyces ambofaciens . J Ind Microbiol Biotechnol 41, 251–263 (2014). https://doi.org/10.1007/s10295-013-1379-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10295-013-1379-y

Keywords

Navigation