This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Adékambi T, Butler RW, Hanrahan F, Delcher AL, Drancourt M, Shinnick TM. Core gene set as the basis of multilocus sequence analysis of the subclass Actinobacteridae. PLoS One. 2011 Mar 31; 6(3):e14792. https://doi.org/10.1371/journal.pone.0014792AdékambiTButlerRWHanrahanFDelcherALDrancourtMShinnickTM. Core gene set as the basis of multilocus sequence analysis of the subclass Actinobacteridae. 2011Mar31; 6(3):e14792. https://doi.org/10.1371/journal.pone.001479210.1371/journal.pone.0014792306900221483493Search in Google Scholar
Ahmed L, Jensen PR, Freel KC, Brown R, Jones AL, Kim BY, Goodfellow M. Salinispora pacifica sp. nov., an actinomycete from marine sediments. Antonie van Leeuwenhoek. 2013 May;103(5): 1069–1078. https://doi.org/10.1007/s10482-013-9886-4AhmedLJensenPRFreelKCBrownRJonesALKimBYGoodfellowM. Salinispora pacifica sp. nov., an actinomycete from marine sediments. 2013May;103(5): 1069–1078. https://doi.org/10.1007/s10482-013-9886-410.1007/s10482-013-9886-423361994Search in Google Scholar
Amin DH, Abdallah NA, Abolmaaty A, Tolba S, Wellington EMH. Microbiological and molecular insights on rare Actinobacteria harboring bioactive prospective. Bull Natl Res Cent. 2020 Dec;44(1):5. https://doi.org/10.1186/s42269-019-0266-8AminDHAbdallahNAAbolmaatyATolbaSWellingtonEMH. Microbiological and molecular insights on rare Actinobacteria harboring bioactive prospective. 2020Dec;44(1):5. https://doi.org/10.1186/s42269-019-0266-810.1186/s42269-019-0266-8Search in Google Scholar
Bérdy J. Thoughts and facts about antibiotics: where we are now and where we are heading. J Antibiot (Tokyo). 2012 Aug;65(8):385–395. https://doi.org/10.1038/ja.2012.27BérdyJ. Thoughts and facts about antibiotics: where we are now and where we are heading. 2012Aug;65(8):385–395. https://doi.org/10.1038/ja.2012.2710.1038/ja.2012.2722511224Search in Google Scholar
Boucher HW, Talbot GH, Bradley JS, Edwards JE, Gilbert D, Rice LB, Scheld M, Spellberg B, Bartlett J. Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America. Clin Infect Dis. 2009 Jan;48(1):1–12. https://doi.org/10.1086/595011BoucherHWTalbotGHBradleyJSEdwardsJEGilbertDRiceLBScheldMSpellbergBBartlettJ. Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America. 2009Jan;48(1):1–12. https://doi.org/10.1086/59501110.1086/59501119035777Search in Google Scholar
Büttner H, Mack D, Rohde H. Structural basis of Staphylococcus epidermidis biofilm formation: mechanisms and molecular interactions. Front Cell Infect Microbiol. 2015 Feb 17;5:14.BüttnerHMackDRohdeH. Structural basis of Staphylococcus epidermidis biofilm formation: mechanisms and molecular interactions. 2015Feb17;5:14.10.3389/fcimb.2015.00014433091825741476Search in Google Scholar
Carro L, Castro JF, Razmilic V, Nouioui I, Pan C, Igual JM, Jaspars M, Goodfellow M, Bull AT, Asenjo JA, et al. Uncovering the potential of novel micromonosporae isolated from an extreme hyper-arid Atacama Desert soil. Sci Rep. 2019 Dec;9(1):4678. https://doi.org/10.1038/s41598-019-38789-zCarroLCastroJFRazmilicVNouiouiIPanCIgualJMJasparsMGoodfellowMBullATAsenjoJA. Uncovering the potential of novel micromonosporae isolated from an extreme hyper-arid Atacama Desert soil. 2019Dec;9(1):4678. https://doi.org/10.1038/s41598-019-38789-z10.1038/s41598-019-38789-z642329130886188Search in Google Scholar
Čihák M, Kameník Z, Šmídová K, Bergman N, Benada O, Kofroňová O, Petříčková K, Bobek J. Secondary metabolites produced during the germination of Streptomyces coelicolor. Front Microbiol. 2017 Dec 13;8:2495. https://doi.org/10.3389/fmicb.2017.02495ČihákMKameníkZŠmídováKBergmanNBenadaOKofroňováOPetříčkováKBobekJ. Secondary metabolites produced during the germination of Streptomyces coelicolor. 2017Dec13;8:2495. https://doi.org/10.3389/fmicb.2017.0249510.3389/fmicb.2017.02495573353229326665Search in Google Scholar
jModelTest 2: more models, new heuristics and parallel computing. Nat Methods. 2012 Aug;9(8):772. https://doi.org/10.1038/nmeth.2109jModelTest 2: more models, new heuristics and parallel computing. 2012Aug;9(8):772. https://doi.org/10.1038/nmeth.210910.1038/nmeth.2109459475622847109Search in Google Scholar
Edlund A, Loesgen S, Fenical W, Jensen PR. Geographic distribution of secondary metabolite genes in the marine actinomycete Salinispora arenicola. Appl Environ Microbiol. 2011 Sep 01;77(17): 5916–5925. https://doi.org/10.1128/AEM.00611-11EdlundALoesgenSFenicalWJensenPR. Geographic distribution of secondary metabolite genes in the marine actinomycete Salinispora arenicola. 2011Sep01;77(17): 5916–5925. https://doi.org/10.1128/AEM.00611-1110.1128/AEM.00611-11316539721724881Search in Google Scholar
Flores-Páez LA, Zenteno JC, Alcántar-Curiel MD, Vargas-Mendoza CF, Rodríguez-Martínez S, Cancino-Diaz ME, Jan-Roblero J, Cancino-Diaz JC. Molecular and phenotypic characterization of Staphylococcus epidermidis isolates from healthy conjunctiva and a comparative analysis with isolates from ocular infection. PLoS One. 2015 Aug 14;10(8):e0135964. https://doi.org/10.1371/journal.pone.0135964Flores-PáezLAZentenoJCAlcántar-CurielMDVargas-MendozaCFRodríguez-MartínezSCancino-DiazMEJan-RobleroJCancino-DiazJC. Molecular and phenotypic characterization of Staphylococcus epidermidis isolates from healthy conjunctiva and a comparative analysis with isolates from ocular infection. 2015Aug14;10(8):e0135964. https://doi.org/10.1371/journal.pone.013596410.1371/journal.pone.0135964453722626275056Search in Google Scholar
Freel KC, Millán-Aguiñaga N, Jensen PR. Multilocus sequence typing reveals evidence of homologous recombination linked to antibiotic resistance in the genus Salinispora. Appl Environ Microbiol. 2013 Oct 01;79(19):5997–6005. https://doi.org/10.1128/AEM.00880-13FreelKCMillán-AguiñagaNJensenPR. Multilocus sequence typing reveals evidence of homologous recombination linked to antibiotic resistance in the genus Salinispora. 2013Oct01;79(19):5997–6005. https://doi.org/10.1128/AEM.00880-1310.1128/AEM.00880-13381135323892741Search in Google Scholar
Genilloud O. Micromonosporaceae. In: Whitman WB, Rainey F, Kämpfer P, Trujillo M, Chun J, DeVos P, Hedlund B, Dedysh S, editors. Bergey’s manual of systematics of archaea and bacteria. Hoboken (USA): John Wiley & Sons, Inc; 2015. p. 1–7.GenilloudO. Micromonosporaceae. In: WhitmanWBRaineyFKämpferPTrujilloMChunJDeVosPHedlundBDedyshS, editors. . Hoboken (USA): John Wiley & Sons, Inc; 2015. p. 1–7.Search in Google Scholar
Gontang EA, Fenical W, Jensen PR. Phylogenetic diversity of gram-positive bacteria cultured from marine sediments. Appl Environ Microbiol. 2007 May 15;73(10):3272–3282. https://doi.org/10.1128/AEM.02811-06GontangEAFenicalWJensenPR. Phylogenetic diversity of gram-positive bacteria cultured from marine sediments. 2007May15;73(10):3272–3282. https://doi.org/10.1128/AEM.02811-0610.1128/AEM.02811-06190711817400789Search in Google Scholar
Goodfellow M, Fiedler HP. A guide to successful bioprospecting: informed by actinobacterial systematics. Antonie van Leeuwenhoek. 2010 Aug;98(2):119–142. https://doi.org/10.1007/s10482-010-9460-2GoodfellowMFiedlerHP. A guide to successful bioprospecting: informed by actinobacterial systematics. 2010Aug;98(2):119–142. https://doi.org/10.1007/s10482-010-9460-210.1007/s10482-010-9460-220582471Search in Google Scholar
Gordon RE, Mihm JM. Identification of Nocardia caviae (Erikson) Nov. Comb.* Ann NY Acad Sci. 1962 Aug;98(3):628–636. https://doi.org/10.1111/j.1749-6632.1962.tb30585.xGordonREMihmJM. Identification of Nocardia caviae (Erikson) Nov. Comb.*1962Aug;98(3):628–636. https://doi.org/10.1111/j.1749-6632.1962.tb30585.x10.1111/j.1749-6632.1962.tb30585.xSearch in Google Scholar
Gouy M, Guindon S, Gascuel O. SeaView version 4: A multiplatform graphical user interface for sequence alignment and phylogenetic tree building. Mol Biol Evol. 2010 Feb 01;27(2):221–224. https://doi.org/10.1093/molbev/msp259GouyMGuindonSGascuelO. SeaView version 4: A multiplatform graphical user interface for sequence alignment and phylogenetic tree building. 2010Feb01;27(2):221–224. https://doi.org/10.1093/molbev/msp25910.1093/molbev/msp25919854763Search in Google Scholar
Guindon S, Dufayard JF, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol. 2010 Mar 29;59(3):307–321. https://doi.org/10.1093/sysbio/syq010GuindonSDufayardJFLefortVAnisimovaMHordijkWGascuelO. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. 2010Mar29;59(3):307–321. https://doi.org/10.1093/sysbio/syq01010.1093/sysbio/syq01020525638Search in Google Scholar
Guindon S, Gascuel O. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol. 2003 Oct 01;52(5):696–704. https://doi.org/10.1080/10635150390235520GuindonSGascuelO. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. 2003Oct01;52(5):696–704. https://doi.org/10.1080/1063515039023552010.1080/1063515039023552014530136Search in Google Scholar
Jensen PR, Maldonado LA, Goodfellow M. Salinispora. In: Whitman WB, Rainey F, Kämpfer P, Trujillo M, Chun J, DeVos P, Hedlund B, Dedysh S, editors. Bergey’s manual of systematics of archaea and bacteria. Hoboken (USA): John Wiley & Sons, Inc; 2015a, p. 1–10.JensenPRMaldonadoLAGoodfellowM. Salinispora. In: WhitmanWBRaineyFKämpferPTrujilloMChunJDeVosPHedlundBDedyshS, editors. . Hoboken (USA): John Wiley & Sons, Inc; 2015a, p. 1–10.Search in Google Scholar
Jensen PR, Moore BS, Fenical W. The marine actinomycete genus Salinispora: a model organism for secondary metabolite discovery. Nat Prod Rep. 2015b;32(5):738–751. https://doi.org/10.1039/C4NP00167BJensenPRMooreBSFenicalW. The marine actinomycete genus Salinispora: a model organism for secondary metabolite discovery. 2015b;32(5):738–751. https://doi.org/10.1039/C4NP00167B10.1039/C4NP00167B441482925730728Search in Google Scholar
Jensen PR, Williams PG, Oh DC, Zeigler L, Fenical W. Species-specific secondary metabolite production in marine actinomycetes of the genus Salinispora. Appl Environ Microbiol. 2007 Feb 15;73(4): 1146–1152. https://doi.org/10.1128/AEM.01891-06JensenPRWilliamsPGOhDCZeiglerLFenicalW. Species-specific secondary metabolite production in marine actinomycetes of the genus Salinispora. 2007Feb15;73(4): 1146–1152. https://doi.org/10.1128/AEM.01891-0610.1128/AEM.01891-06182864517158611Search in Google Scholar
Jensen PR. Natural products and the gene cluster revolution. Trends Microbiol. 2016 Dec;24(12):968–977. https://doi.org/10.1016/j.tim.2016.07.006JensenPR. Natural products and the gene cluster revolution. 2016Dec;24(12):968–977. https://doi.org/10.1016/j.tim.2016.07.00610.1016/j.tim.2016.07.006512393427491886Search in Google Scholar
Jose PA, Jebakumar SRD. Non-streptomycete actinomycetes nourish the current microbial antibiotic drug discovery. Front Microbiol. 2013;4:240. https://doi.org/10.3389/fmicb.2013.00240JosePAJebakumarSRD. Non-streptomycete actinomycetes nourish the current microbial antibiotic drug discovery. 2013;4:240. https://doi.org/10.3389/fmicb.2013.0024010.3389/fmicb.2013.00240374735423970883Search in Google Scholar
Jose PA, Jha B. Intertidal marine sediment harbours Actinobacteria with promising bioactive and biosynthetic potential. Sci Rep. 2017 Dec;7(1):10041. https://doi.org/10.1038/s41598-017-09672-6JosePAJhaB. Intertidal marine sediment harbours Actinobacteria with promising bioactive and biosynthetic potential. 2017Dec;7(1):10041. https://doi.org/10.1038/s41598-017-09672-610.1038/s41598-017-09672-6557723028855551Search in Google Scholar
Kim TK, Hewavitharana AK, Shaw PN, Fuerst JA. Discovery of a new source of rifamycin antibiotics in marine sponge actinobacteria by phylogenetic prediction. Appl Environ Microbiol. 2006 Mar; 72(3):2118–2125. https://doi.org/10.1128/AEM.72.3.2118-2125.2006KimTKHewavitharanaAKShawPNFuerstJA. Discovery of a new source of rifamycin antibiotics in marine sponge actinobacteria by phylogenetic prediction. 2006Mar; 72(3):2118–2125. https://doi.org/10.1128/AEM.72.3.2118-2125.200610.1128/AEM.72.3.2118-2125.2006139324316517661Search in Google Scholar
Lane DJ. 16S/23S rRNA sequencing. In: Stackenbrandt E, Goodfellow M, editors. Nucleic acid techniques in bacterial systematics. New York (USA): Wiley; 1991.LaneDJ. 16S/23S rRNA sequencing. In: StackenbrandtEGoodfellowM, editors. . New York (USA): Wiley; 1991.Search in Google Scholar
Maldonado LA, Fenical W, Jensen PR, Kauffman CA, Mincer TJ, Ward AC, Bull AT, Goodfellow M. Salinispora arenicola gen. nov., sp. nov. and Salinispora tropica sp. nov., obligate marine actinomycetes belonging to the family Micromonosporaceae. Int J Syst Evol Microbiol. 2005a Sep 01;55(5):1759–1766. https://doi.org/10.1099/ijs.0.63625-0MaldonadoLAFenicalWJensenPRKauffmanCAMincerTJWardACBullATGoodfellowM. Salinispora arenicola gen. nov., sp. nov. and Salinispora tropica sp. nov., obligate marine actinomycetes belonging to the family Micromonosporaceae. 2005aSep01;55(5):1759–1766. https://doi.org/10.1099/ijs.0.63625-010.1099/ijs.0.63625-016166663Search in Google Scholar
Maldonado LA, Fragoso-Yáñez D, Pérez-García A, Rosellón-Druker J, Quintana ET. Actinobacterial diversity from marine sediments collected in Mexico. Antonie van Leeuwenhoek. 2009 Feb;95(2):111–120. https://doi.org/10.1007/s10482-008-9294-3MaldonadoLAFragoso-YáñezDPérez-GarcíaARosellón-DrukerJQuintanaET. Actinobacterial diversity from marine sediments collected in Mexico. 2009Feb;95(2):111–120. https://doi.org/10.1007/s10482-008-9294-310.1007/s10482-008-9294-319023674Search in Google Scholar
Maldonado LA, Quintana ET. Unexpected properties of Micromonosporae from marine origin. Adv Microbiol. 2015;05(06): 452–456. https://doi.org/10.4236/aim.2015.56046MaldonadoLAQuintanaET. Unexpected properties of Micromonosporae from marine origin. 2015;05(06): 452–456. https://doi.org/10.4236/aim.2015.5604610.4236/aim.2015.56046Search in Google Scholar
Maldonado LA, Stach JEM, Pathom-aree W, Ward AC, Bull AT, Goodfellow M. Diversity of cultivable actinobacteria in geographically widespread marine sediments. Antonie van Leeuwenhoek. 2005b Jan;87(1):11–18. https://doi.org/10.1007/s10482-004-6525-0MaldonadoLAStachJEMPathom-areeWWardACBullATGoodfellowM. Diversity of cultivable actinobacteria in geographically widespread marine sediments. 2005bJan;87(1):11–18. https://doi.org/10.1007/s10482-004-6525-010.1007/s10482-004-6525-015726286Search in Google Scholar
McCann MT, Gilmore BF, Gorman SP. Staphylococcus epidermidis device-related infections: pathogenesis and clinical management. J Pharm Pharmacol. 2008 Dec;60(12):1551–1571. https://doi.org/10.1211/jpp.60.12.0001McCannMTGilmoreBFGormanSP. Staphylococcus epidermidis device-related infections: pathogenesis and clinical management. 2008Dec;60(12):1551–1571. https://doi.org/10.1211/jpp.60.12.000110.1211/jpp/60.12.000119000360Search in Google Scholar
Millán-Aguiñaga N, Chavarria KL, Ugalde JA, Letzel AC, Rouse GW, Jensen PR. Phylogenomic insight into Salinispora (Bacteria, Actinobacteria) species designations. Sci Rep. 2017 Dec;7(1): 3564. https://doi.org/10.1038/s41598-017-02845-3Millán-AguiñagaNChavarriaKLUgaldeJALetzelACRouseGWJensenPR. Phylogenomic insight into Salinispora (Bacteria, Actinobacteria) species designations. 2017Dec;7(1): 3564. https://doi.org/10.1038/s41598-017-02845-310.1038/s41598-017-02845-3547263328620214Search in Google Scholar
Mincer TJ, Jensen PR, Kauffman CA, Fenical W. Widespread and persistent populations of a major new marine actinomycete taxon in ocean sediments. Appl Environ Microbiol. 2002 Oct;68(10): 5005–5011. https://doi.org/10.1128/AEM.68.10.5005-5011.2002MincerTJJensenPRKauffmanCAFenicalW. Widespread and persistent populations of a major new marine actinomycete taxon in ocean sediments. 2002Oct;68(10): 5005–5011. https://doi.org/10.1128/AEM.68.10.5005-5011.200210.1128/AEM.68.10.5005-5011.200212640412324350Search in Google Scholar
Partridge SR, Kwong SM, Firth N, Jensen SO. Mobile genetic elements associated with antimicrobial resistance. Clin Microbiol Rev. 2018 Aug 01;31(4):e00088-17. https://doi.org/10.1128/CMR.00088-17PartridgeSRKwongSMFirthNJensenSO. Mobile genetic elements associated with antimicrobial resistance. 2018Aug01;31(4):e00088-17. https://doi.org/10.1128/CMR.00088-1710.1128/CMR.00088-17614819030068738Search in Google Scholar
Pendleton JN, Gorman SP, Gilmore BF. Clinical relevance of the ESKAPE pathogens. Expert Rev Anti Infect Ther. 2013 Mar;11(3): 297–308. https://doi.org/10.1586/eri.13.12PendletonJNGormanSPGilmoreBF. Clinical relevance of the ESKAPE pathogens. 2013Mar;11(3): 297–308. https://doi.org/10.1586/eri.13.1210.1586/eri.13.1223458769Search in Google Scholar
Quintana ET, Gil-Rivera DA, Alejo-Viderique A, López-Villegas O, Maldonado LA. Evaluation of the antifungal and antiyeast activities from recently isolated Streptomycetes. J Pharm Biomed Sci. 2015;5(11):867–876.QuintanaETGil-RiveraDAAlejo-VideriqueALópez-VillegasOMaldonadoLA. Evaluation of the antifungal and antiyeast activities from recently isolated Streptomycetes. 2015;5(11):867–876.Search in Google Scholar
Richardson PG, Zimmerman TM, Hofmeister CC, Talpaz M, Chanan-Khan AA, Kaufman JL, Laubach JP, Chauhan D, Jakubowiak AJ, Reich S, et al. Phase 1 study of marizomib in relapsed or relapsed and refractory multiple myeloma: NPI-0052-101 Part 1. Blood. 2016 Jun 02;127(22):2693–2700. https://doi.org/10.1182/blood-2015-12-686378RichardsonPGZimmermanTMHofmeisterCCTalpazMChanan-KhanAAKaufmanJLLaubachJPChauhanDJakubowiakAJReichS. Phase 1 study of marizomib in relapsed or relapsed and refractory multiple myeloma: NPI-0052-101 Part 1. 2016Jun02;127(22):2693–2700. https://doi.org/10.1182/blood-2015-12-68637810.1182/blood-2015-12-686378541329627009059Search in Google Scholar
Rong X, Huang Y. Multi-locus sequence analysis. In: Goodfellow M, Sutcliffe I, Chun J, editors. New approaches to prokaryotic systematics. London: Academic Press. 2014. pp. 221–251.RongXHuangY. Multi-locus sequence analysis. In: GoodfellowMSutcliffeIChunJ, editors. . London: Academic Press. 2014. pp. 221–251.10.1016/bs.mim.2014.10.001Search in Google Scholar
Shirling EB, Gottlieb D. Methods for characterization of Streptomyces species. Int J Syst Evol Microbiol. 1966;16(3):313–340.ShirlingEBGottliebD. Methods for characterization of Streptomyces species. 1966;16(3):313–340.Search in Google Scholar
Stackebrandt E, Rainey FA, Ward-Rainey NL. Proposal for a new hierarchic classification system, Actinobacteria classis nov. Int J Syst Bacteriol. 1997 Apr 01;47(2):479–491. https://doi.org/10.1099/00207713-47-2-479StackebrandtERaineyFAWard-RaineyNL. Proposal for a new hierarchic classification system, Actinobacteria classis nov. 1997Apr01;47(2):479–491. https://doi.org/10.1099/00207713-47-2-47910.1099/00207713-47-2-479Search in Google Scholar
Subramani R, Sipkema D. Marine rare actinomycetes: A promising source of structurally diverse and unique novel natural products. Mar Drugs. 2019 Apr 26;17(5):249. https://doi.org/10.3390/md17050249SubramaniRSipkemaD. Marine rare actinomycetes: A promising source of structurally diverse and unique novel natural products. 2019Apr26;17(5):249. https://doi.org/10.3390/md1705024910.3390/md17050249656266431035452Search in Google Scholar
Suchard MA, Lemey P, Baele G, Ayres DL, Drummond AJ, Rambaut A. Bayesian phylogenetic and phylodynamic data integration using BEAST 1.10. Virus Evol. 2018 Jan 01;4(1):vey016. https://doi.org/10.1093/ve/vey016SuchardMALemeyPBaeleGAyresDLDrummondAJRambautA. Bayesian phylogenetic and phylodynamic data integration using BEAST 1.10. 2018Jan01;4(1):vey016. https://doi.org/10.1093/ve/vey01610.1093/ve/vey016600767429942656Search in Google Scholar
Udwary DW, Zeigler L, Asolkar RN, Singan V, Lapidus A, Fenical W, Jensen PR, Moore BS. Genome sequencing reveals complex secondary metabolome in the marine actinomycete Salinispora tropica. Proc Natl Acad Sci USA. 2007 Jun 19;104(25):10376–10381. https://doi.org/10.1073/pnas.0700962104UdwaryDWZeiglerLAsolkarRNSinganVLapidusAFenicalWJensenPRMooreBS. Genome sequencing reveals complex secondary metabolome in the marine actinomycete Salinispora tropica. 2007Jun19;104(25):10376–10381. https://doi.org/10.1073/pnas.070096210410.1073/pnas.0700962104196552117563368Search in Google Scholar
Versalovic J, Schneider M, De Bruijn FJ, Lupski JR. Genomic fingerprinting of bacteria using repetitive sequence-based polymerase chain reaction. Methods Mol Cell Biol. 1994;5(1):25–40.VersalovicJSchneiderMDe BruijnFJLupskiJR. Genomic fingerprinting of bacteria using repetitive sequence-based polymerase chain reaction. 1994;5(1):25–40.Search in Google Scholar
Vidgen ME, Hooper JNA, Fuerst JA. Diversity and distribution of the bioactive actinobacterial genus Salinispora from sponges along the Great Barrier Reef. Antonie van Leeuwenhoek. 2012 Mar;101(3):603–618. https://doi.org/10.1007/s10482-011-9676-9VidgenMEHooperJNAFuerstJA. Diversity and distribution of the bioactive actinobacterial genus Salinispora from sponges along the Great Barrier Reef. 2012Mar;101(3):603–618. https://doi.org/10.1007/s10482-011-9676-910.1007/s10482-011-9676-922094709Search in Google Scholar
Weinhäupl K, Brennich M, Kazmaier U, Lelievre J, Ballell L, Goldberg A, Schanda P, Fraga H. The antibiotic cyclomarin blocks arginine-phosphate-induced millisecond dynamics in the N-terminal domain of ClpC1 from Mycobacterium tuberculosis. J Biol Chem. 2018 Jun 01;293(22):8379–8393. https://doi.org/10.1074/jbc.RA118.002251WeinhäuplKBrennichMKazmaierULelievreJBallellLGoldbergASchandaPFragaH. The antibiotic cyclomarin blocks arginine-phosphate-induced millisecond dynamics in the N-terminal domain of ClpC1 from Mycobacterium tuberculosis. 2018Jun01;293(22):8379–8393. https://doi.org/10.1074/jbc.RA118.00225110.1074/jbc.RA118.002251598621729632076Search in Google Scholar
Wiese J, Jiang Y, Tang SK, Thiel V, Schmaljohann R, Xu LH, Jiang CL, Imhoff JF. A new member of the family Micromonosporaceae, Planosporangium flavigriseum gen. nov., sp. nov. Int J Syst Evol Microbiol. 2008 Jun 01;58(6):1324–1331. https://doi.org/10.1099/ijs.0.65211-0WieseJJiangYTangSKThielVSchmaljohannRXuLHJiangCLImhoffJF. A new member of the family Micromonosporaceae, Planosporangium flavigriseum gen. nov., sp. nov. 2008Jun01;58(6):1324–1331. https://doi.org/10.1099/ijs.0.65211-010.1099/ijs.0.65211-018523173Search in Google Scholar
WHO. Global priority list of antibiotic-resistant bacteria to guide research, discovery, and development of new antibiotics [Internet]. Geneva (Switzerland): World Health Organization; 2017 [cited 2020 Feb 17]. Available from https://www.who.int/medicines/publications/global-priority-list-antibiotic-resistant-bacteria/enWHO. . Geneva (Switzerland): World Health Organization; 2017[cited 2020 Feb 17]. Available fromhttps://www.who.int/medicines/publications/global-priority-list-antibiotic-resistant-bacteria/enSearch in Google Scholar
Ziemert N, Lechner A, Wietz M, Millán-Aguiñaga N, Chavarria KL, Jensen PR. Diversity and evolution of secondary metabolism in the marine actinomycete genus Salinispora. Proc Natl Acad Sci USA. 2014 Mar 25;111(12):E1130–E1139. https://doi.org/10.1073/pnas.1324161111ZiemertNLechnerAWietzMMillán-AguiñagaNChavarriaKLJensenPR. Diversity and evolution of secondary metabolism in the marine actinomycete genus Salinispora. 2014Mar25;111(12):E1130–E1139. https://doi.org/10.1073/pnas.132416111110.1073/pnas.1324161111397052524616526Search in Google Scholar