메뉴 건너뛰기




Volumn 38, Issue 1, 2014, Pages 172-188

Marine actinobacteria: An important source of bioactive natural products

Author keywords

Antibiotics; Bioactive compounds; Chemical structures; Marine actinobacteria; Natural products

Indexed keywords

8 AMINO [1,4]DIAZONANE 2,5 DIONE; ABYSSOMICIN C; ACTINOFURANONE DERIVATIVE; ARENAMIDE DERIVATIVE; ARENICOLIDE DERIVATIVE; AZAMERONE; CHALCOMYCIN A; CHARTREUSIN; CYCLOMARIN A; DARYAMIDE DERIVATIVE; GLYCIAPYRROLE DERIVATIVE; GRISEORHODIN A; HIMALOMYCIN DERIVATIVE; KOMODOQUINONE A; LEUCYL 4 HYDROXYPROLINE; LUCENTAMYCIN DERIVATIVE; MECHERCHARMYCIN DERIVATIVE; NATURAL PRODUCT; PACIFICANONE DERIVATIVE; PHAEOCHROMYCIN DERIVATIVE; PIPERAZIMYCIN DERIVATIVE; POLYKETIDE; PROXIMICIN DERIVATIVE; SALINAMIDE DERIVATIVE; SALINIKETAL; SALINIPYRONE DERIVATIVE; SELINA 4(14),7(11) DIENE 8,9 DIO; TETRACENOMYCIN D; THIOCORALINE; UNCLASSIFIED DRUG; UNINDEXED DRUG; BIOLOGICAL PRODUCT;

EID: 84902982808     PISSN: 13826689     EISSN: 18727077     Source Type: Journal    
DOI: 10.1016/j.etap.2014.05.014     Document Type: Review
Times cited : (125)

References (79)
  • 3
    • 33846422344 scopus 로고    scopus 로고
    • Daryamides AC, weakly cytotoxic polyketides from a marine-derived actinomycete of the genus Streptomyces strain CNQ-085
    • Asolkar R.N., Jensen P.R., Kauffman C.A., Fenical W. Daryamides AC, weakly cytotoxic polyketides from a marine-derived actinomycete of the genus Streptomyces strain CNQ-085. J. Nat. Prod. 2006, 69:1756-1759.
    • (2006) J. Nat. Prod. , vol.69 , pp. 1756-1759
    • Asolkar, R.N.1    Jensen, P.R.2    Kauffman, C.A.3    Fenical, W.4
  • 4
    • 0036807226 scopus 로고    scopus 로고
    • Chalcomycin B, a new macrolide antibiotic from the marine isolate Streptomyces sp. B7064
    • Asolkar R.N., Maskey R.P., Helmke E., Laatsch H. Chalcomycin B, a new macrolide antibiotic from the marine isolate Streptomyces sp. B7064. J. Antibiot. 2002, 55:893-898.
    • (2002) J. Antibiot. , vol.55 , pp. 893-898
    • Asolkar, R.N.1    Maskey, R.P.2    Helmke, E.3    Laatsch, H.4
  • 5
    • 0013617464 scopus 로고    scopus 로고
    • Aburatubolactam A, a novel inhibitor of superoxide anion generation from a marine microorganism
    • Bae M., Yamada K., Ijuin Y., Tsuji T., Yazawa K., Uemura D. Aburatubolactam A, a novel inhibitor of superoxide anion generation from a marine microorganism. Heterocycl. Commun. 1996, 2:315-318.
    • (1996) Heterocycl. Commun. , vol.2 , pp. 315-318
    • Bae, M.1    Yamada, K.2    Ijuin, Y.3    Tsuji, T.4    Yazawa, K.5    Uemura, D.6
  • 6
    • 54849405130 scopus 로고    scopus 로고
    • Renaissance in antibacterial discovery from actinomycetes
    • Baltz R.H. Renaissance in antibacterial discovery from actinomycetes. Curr. Opin. Pharmacol. 2008, 8:557-563.
    • (2008) Curr. Opin. Pharmacol. , vol.8 , pp. 557-563
    • Baltz, R.H.1
  • 11
    • 33745731337 scopus 로고    scopus 로고
    • Bountiful oceans. Prospecting marine microbial diversity
    • Bull A. Bountiful oceans. Prospecting marine microbial diversity. Scr. Trends Drug Discov. 2004, 5:14-16.
    • (2004) Scr. Trends Drug Discov. , vol.5 , pp. 14-16
    • Bull, A.1
  • 13
    • 33644535147 scopus 로고    scopus 로고
    • Natural products-the future scaffolds for novel antibiotics?
    • Butler M.S., Buss A.D. Natural products-the future scaffolds for novel antibiotics?. Biochem. Pharmacol. 2006, 71:919-929.
    • (2006) Biochem. Pharmacol. , vol.71 , pp. 919-929
    • Butler, M.S.1    Buss, A.D.2
  • 14
    • 33745575317 scopus 로고    scopus 로고
    • Azamerone, a terpenoid phthalazinone from a marine-derived bacterium related to the genus Streptomyces (Actinomycetales)
    • Cho J.Y., Kwon H.C., Williams P.G., Jensen P.R., Fenical W. Azamerone, a terpenoid phthalazinone from a marine-derived bacterium related to the genus Streptomyces (Actinomycetales). Org. Lett. 2006, 8:2471-2474.
    • (2006) Org. Lett. , vol.8 , pp. 2471-2474
    • Cho, J.Y.1    Kwon, H.C.2    Williams, P.G.3    Jensen, P.R.4    Fenical, W.5
  • 15
    • 33645976832 scopus 로고    scopus 로고
    • Actinofuranones A and B, polyketides from a marine-derived bacterium related to the genus Streptomyces (Actinomycetales)
    • Cho J.Y., Kwon H.C., Williams P.G., Kauffman C.A., Jensen P.R., Fenical W. Actinofuranones A and B, polyketides from a marine-derived bacterium related to the genus Streptomyces (Actinomycetales). J. Nat. Prod. 2006, 69:425-428.
    • (2006) J. Nat. Prod. , vol.69 , pp. 425-428
    • Cho, J.Y.1    Kwon, H.C.2    Williams, P.G.3    Kauffman, C.A.4    Jensen, P.R.5    Fenical, W.6
  • 16
    • 34548627224 scopus 로고    scopus 로고
    • Lucentamycins AD, cytotoxic peptides from the marine-derived actinomycete Nocardiopsis lucentensis
    • Cho J.Y., Williams P.G., Kwon H.C., Jensen P.R., Fenical W. Lucentamycins AD, cytotoxic peptides from the marine-derived actinomycete Nocardiopsis lucentensis. J. Nat. Prod. 2007, 70:1321-1328.
    • (2007) J. Nat. Prod. , vol.70 , pp. 1321-1328
    • Cho, J.Y.1    Williams, P.G.2    Kwon, H.C.3    Jensen, P.R.4    Fenical, W.5
  • 17
    • 60549103927 scopus 로고    scopus 로고
    • T-muurolol sesquiterpenes from the marine Streptomyces sp. M491 and revision of the configuration of previously reported amorphanes
    • Ding L., Pfoh R., Rühl S., Qin S., Laatsch H. T-muurolol sesquiterpenes from the marine Streptomyces sp. M491 and revision of the configuration of previously reported amorphanes. J. Nat. Prod. 2008, 72:99-101.
    • (2008) J. Nat. Prod. , vol.72 , pp. 99-101
    • Ding, L.1    Pfoh, R.2    Rühl, S.3    Qin, S.4    Laatsch, H.5
  • 19
    • 0030092407 scopus 로고    scopus 로고
    • From chemistry of marine natural products to marine technologies: research at the Pacific Institute of Bioorganic Chemistry
    • Elyakov G.B., Stonik V.A., Kuznetsova T.A., Mikhailov V.V. From chemistry of marine natural products to marine technologies: research at the Pacific Institute of Bioorganic Chemistry. Mar. Technol. Soc. J. 1996, 30:21-28.
    • (1996) Mar. Technol. Soc. J. , vol.30 , pp. 21-28
    • Elyakov, G.B.1    Stonik, V.A.2    Kuznetsova, T.A.3    Mikhailov, V.V.4
  • 20
    • 33751100882 scopus 로고    scopus 로고
    • Developing a new resource for drug discovery: marine actinomycete bacteria
    • Fenical W., Jensen P.R. Developing a new resource for drug discovery: marine actinomycete bacteria. Nat. Chem. Biol. 2006, 2:666-673.
    • (2006) Nat. Chem. Biol. , vol.2 , pp. 666-673
    • Fenical, W.1    Jensen, P.R.2
  • 23
    • 84857237177 scopus 로고    scopus 로고
    • Isolation strategies of marine-derived actinomycetes from sponge and sediment samples
    • Hameş-Kocabaş E., Uzel A. Isolation strategies of marine-derived actinomycetes from sponge and sediment samples. J. Microbiol. Methods 2012, 88:342-347.
    • (2012) J. Microbiol. Methods , vol.88 , pp. 342-347
    • Hameş-Kocabaş, E.1    Uzel, A.2
  • 24
    • 0034719903 scopus 로고    scopus 로고
    • Neomarinone, and new cytotoxic marinone derivatives, produced by a marine filamentous bacterium (actinomycetales)
    • Hardt I.H., Jensen P.R., Fenical W. Neomarinone, and new cytotoxic marinone derivatives, produced by a marine filamentous bacterium (actinomycetales). Tetrahedron Lett. 2000, 41:2073-2076.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 2073-2076
    • Hardt, I.H.1    Jensen, P.R.2    Fenical, W.3
  • 28
    • 58249097269 scopus 로고    scopus 로고
    • The ammosamides: structures of cell cycle modulators from a marine-derived Streptomyces species
    • Hughes C.C., MacMillan J.B., Gaudêncio S.P., Jensen P.R., Fenical W. The ammosamides: structures of cell cycle modulators from a marine-derived Streptomyces species. Angew. Chem. Int. Ed. 2009, 48:725-727.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 725-727
    • Hughes, C.C.1    MacMillan, J.B.2    Gaudêncio, S.P.3    Jensen, P.R.4    Fenical, W.5
  • 29
    • 39749179651 scopus 로고    scopus 로고
    • The marinopyrroles, antibiotics of an unprecedented structure class from a marine Streptomyces sp.
    • Hughes C.C., Prieto-Davo A., Jensen P.R., Fenical W. The marinopyrroles, antibiotics of an unprecedented structure class from a marine Streptomyces sp. Org. Lett. 2008, 10:629-631.
    • (2008) Org. Lett. , vol.10 , pp. 629-631
    • Hughes, C.C.1    Prieto-Davo, A.2    Jensen, P.R.3    Fenical, W.4
  • 30
    • 14744303284 scopus 로고    scopus 로고
    • Enzyme inhibitors and other bioactive compounds from marine actinomycetes
    • Imada C. Enzyme inhibitors and other bioactive compounds from marine actinomycetes. Antonie Van Leeuwenhoek 2005, 87:59-63.
    • (2005) Antonie Van Leeuwenhoek , vol.87 , pp. 59-63
    • Imada, C.1
  • 31
    • 0142156725 scopus 로고    scopus 로고
    • Komodoquinone A, a novel neuritogenic anthracycline, from marine Streptomyces sp. KS3
    • Itoh T., Kinoshita M., Aoki S., Kobayashi M. Komodoquinone A, a novel neuritogenic anthracycline, from marine Streptomyces sp. KS3. J. Nat. Prod. 2003, 66:1373-1377.
    • (2003) J. Nat. Prod. , vol.66 , pp. 1373-1377
    • Itoh, T.1    Kinoshita, M.2    Aoki, S.3    Kobayashi, M.4
  • 32
    • 2942727746 scopus 로고    scopus 로고
    • Stereostructure of komodoquinone A, a neuritogenic anthracycline, from marine Streptomyces sp. KS3
    • Itoh T., Kinoshita M., Wei H., Kobayashi M. Stereostructure of komodoquinone A, a neuritogenic anthracycline, from marine Streptomyces sp. KS3. Chem. Pharm. Bull. 2003, 51:1402-1404.
    • (2003) Chem. Pharm. Bull. , vol.51 , pp. 1402-1404
    • Itoh, T.1    Kinoshita, M.2    Wei, H.3    Kobayashi, M.4
  • 33
    • 34548510609 scopus 로고    scopus 로고
    • Isolation and structure determination of streptochlorin, an antiproliferative agent from a marine-derived Streptomyces sp. 04DH110
    • Jae S.H., Jeong H.S., Lee H.-S., Park S.-K., Kim H.M., Kwon H.J. Isolation and structure determination of streptochlorin, an antiproliferative agent from a marine-derived Streptomyces sp. 04DH110. J. Microbiol. Biotechnol. 2007, 17:1403-1406.
    • (2007) J. Microbiol. Biotechnol. , vol.17 , pp. 1403-1406
    • Jae, S.H.1    Jeong, H.S.2    Lee, H.-S.3    Park, S.-K.4    Kim, H.M.5    Kwon, H.J.6
  • 34
    • 20444488858 scopus 로고    scopus 로고
    • Culturable marine actinomycete diversity from tropical Pacific Ocean sediments
    • Jensen P.R., Gontang E., Mafnas C., Mincer T.J., Fenical W. Culturable marine actinomycete diversity from tropical Pacific Ocean sediments. Environ. Microbiol. 2005, 7:1039-1048.
    • (2005) Environ. Microbiol. , vol.7 , pp. 1039-1048
    • Jensen, P.R.1    Gontang, E.2    Mafnas, C.3    Mincer, T.J.4    Fenical, W.5
  • 35
    • 33847186292 scopus 로고    scopus 로고
    • Species-specific secondary metabolite production in marine actinomycetes of the genus Salinispora
    • Jensen P.R., Williams P.G., Oh D.C., Zeigler L., Fenical W. Species-specific secondary metabolite production in marine actinomycetes of the genus Salinispora. Appl. Environ. Microbiol. 2007, 73:1146-1152.
    • (2007) Appl. Environ. Microbiol. , vol.73 , pp. 1146-1152
    • Jensen, P.R.1    Williams, P.G.2    Oh, D.C.3    Zeigler, L.4    Fenical, W.5
  • 36
    • 33744958864 scopus 로고    scopus 로고
    • Streptokordin, a new cytotoxic compound of the methylpyridine class from a marine-derived Streptomyces sp. KORDI-3238
    • Jeong S.-Y., Shin H.J., Kim T.S., Lee H.-S., Park S.-K., Kim H.M. Streptokordin, a new cytotoxic compound of the methylpyridine class from a marine-derived Streptomyces sp. KORDI-3238. J. Antibiot. 2006, 59:234-240.
    • (2006) J. Antibiot. , vol.59 , pp. 234-240
    • Jeong, S.-Y.1    Shin, H.J.2    Kim, T.S.3    Lee, H.-S.4    Park, S.-K.5    Kim, H.M.6
  • 37
    • 19644386054 scopus 로고    scopus 로고
    • Mechercharmycins A and B, cytotoxic substances from marine-derived Thermoactinomyces sp. YM3-251
    • Kanoh K., Matsuo Y., Adachi K., Imagawa H., Nishizawa M., Shizuri Y. Mechercharmycins A and B, cytotoxic substances from marine-derived Thermoactinomyces sp. YM3-251. J. Antibiot. 2005, 58:289-292.
    • (2005) J. Antibiot. , vol.58 , pp. 289-292
    • Kanoh, K.1    Matsuo, Y.2    Adachi, K.3    Imagawa, H.4    Nishizawa, M.5    Shizuri, Y.6
  • 38
    • 33744537287 scopus 로고    scopus 로고
    • Discovery of novel metabolites from marine actinomycetes
    • Lam K.S. Discovery of novel metabolites from marine actinomycetes. Curr. Opin. Microbiol. 2006, 9:245-251.
    • (2006) Curr. Opin. Microbiol. , vol.9 , pp. 245-251
    • Lam, K.S.1
  • 39
    • 0036753178 scopus 로고    scopus 로고
    • A gene cluster from a marine Streptomyces encoding the biosynthesis of the aromatic spiroketal polyketide Griseorhodin A
    • Li A., Piel J. A gene cluster from a marine Streptomyces encoding the biosynthesis of the aromatic spiroketal polyketide Griseorhodin A. Chem. Biol. 2002, 9:1017-1026.
    • (2002) Chem. Biol. , vol.9 , pp. 1017-1026
    • Li, A.1    Piel, J.2
  • 40
    • 33748343651 scopus 로고    scopus 로고
    • Four butenolides are novel cytotoxic compounds isolated from the marine-derived bacterium, Streptoverticillium luteoverticillatum 11014
    • Li D.-H., Zhu T.-J., Liu H.-B., Fang Y.-C., Gu Q.-Q., Zhu W.-M. Four butenolides are novel cytotoxic compounds isolated from the marine-derived bacterium, Streptoverticillium luteoverticillatum 11014. Arch. Pharm. Res. 2006, 29:624-626.
    • (2006) Arch. Pharm. Res. , vol.29 , pp. 624-626
    • Li, D.-H.1    Zhu, T.-J.2    Liu, H.-B.3    Fang, Y.-C.4    Gu, Q.-Q.5    Zhu, W.-M.6
  • 41
    • 17444374224 scopus 로고    scopus 로고
    • Chinikomycins A and B: isolation, structure elucidation, and biological activity of novel antibiotics from a marine Streptomyces sp. isolate M045
    • Li F., Maskey R.P., Qin S., Sattler I., Fiebig H.H., Maier A., Zeeck A., Laatsch H. Chinikomycins A and B: isolation, structure elucidation, and biological activity of novel antibiotics from a marine Streptomyces sp. isolate M045. J. Nat. Prod. 2005, 68:349-353.
    • (2005) J. Nat. Prod. , vol.68 , pp. 349-353
    • Li, F.1    Maskey, R.P.2    Qin, S.3    Sattler, I.4    Fiebig, H.H.5    Maier, A.6    Zeeck, A.7    Laatsch, H.8
  • 42
    • 79251523549 scopus 로고    scopus 로고
    • Phaeochromycins F-H, three new polyketide metabolites from Streptomyces sp. DSS-18
    • Li J., Lu C.-H., Zhao B.-B., Zheng Z.-H., Shen Y.-M. Phaeochromycins F-H, three new polyketide metabolites from Streptomyces sp. DSS-18. Beilstein J. Org. Chem. 2008, 4:46-50.
    • (2008) Beilstein J. Org. Chem. , vol.4 , pp. 46-50
    • Li, J.1    Lu, C.-H.2    Zhao, B.-B.3    Zheng, Z.-H.4    Shen, Y.-M.5
  • 44
    • 70449529783 scopus 로고    scopus 로고
    • Characterization and identification of a novel marine Streptomyces sp. produced antibacterial substance
    • Lu Y., Dong X., Liu S., Bie X. Characterization and identification of a novel marine Streptomyces sp. produced antibacterial substance. Mar. Biotechnol. 2009, 11:717-724.
    • (2009) Mar. Biotechnol. , vol.11 , pp. 717-724
    • Lu, Y.1    Dong, X.2    Liu, S.3    Bie, X.4
  • 45
    • 20444457998 scopus 로고    scopus 로고
    • Glaciapyrroles A, B, and C, pyrrolosesquiterpenes from a Streptomyces sp. isolated from an Alaskan marine sediment
    • Macherla V.R., Liu J., Bellows C., Teisan S., Nicholson B., Lam K.S., Barbara C. Glaciapyrroles A, B, and C, pyrrolosesquiterpenes from a Streptomyces sp. isolated from an Alaskan marine sediment. J. Nat. Prod. 2005, 68:780-783.
    • (2005) J. Nat. Prod. , vol.68 , pp. 780-783
    • Macherla, V.R.1    Liu, J.2    Bellows, C.3    Teisan, S.4    Nicholson, B.5    Lam, K.S.6    Barbara, C.7
  • 47
    • 84878121979 scopus 로고    scopus 로고
    • Marine actinobacterial metabolites: current status and future perspectives
    • Manivasagan P., Venkatesan J., Sivakumar K., Kim S.-K. Marine actinobacterial metabolites: current status and future perspectives. Microbiol. Res. 2013, 168:311-332.
    • (2013) Microbiol. Res. , vol.168 , pp. 311-332
    • Manivasagan, P.1    Venkatesan, J.2    Sivakumar, K.3    Kim, S.-K.4
  • 48
    • 84894298829 scopus 로고    scopus 로고
    • Pharmaceutically active secondary metabolites of marine actinobacteria
    • Manivasagan P., Venkatesan J., Sivakumar K., Kim S.-K. Pharmaceutically active secondary metabolites of marine actinobacteria. Microbiol. Res. 2014, 169(26):262-278.
    • (2014) Microbiol. Res. , vol.169 , Issue.26 , pp. 262-278
    • Manivasagan, P.1    Venkatesan, J.2    Sivakumar, K.3    Kim, S.-K.4
  • 49
    • 12444253044 scopus 로고    scopus 로고
    • Anti-cancer and antibacterial trioxacarcins with high anti-malaria activity from a marine Streptomycete and their absolute stereochemistry
    • Maskey R.P., Helmke E., Kayser O., Fiebig H.H., Maier A., Busche A., Laatsch H. Anti-cancer and antibacterial trioxacarcins with high anti-malaria activity from a marine Streptomycete and their absolute stereochemistry. J. Antibiot. 2004, 57:771-779.
    • (2004) J. Antibiot. , vol.57 , pp. 771-779
    • Maskey, R.P.1    Helmke, E.2    Kayser, O.3    Fiebig, H.H.4    Maier, A.5    Busche, A.6    Laatsch, H.7
  • 50
    • 0345116079 scopus 로고    scopus 로고
    • Himalomycin A and B: isolation and structure elucidation of new fridamycin type antibiotics from a marine Streptomyces isolate
    • Maskey R.P., Helmke E., Laatsch H. Himalomycin A and B: isolation and structure elucidation of new fridamycin type antibiotics from a marine Streptomyces isolate. J. Antibiot. 2003, 56:942-949.
    • (2003) J. Antibiot. , vol.56 , pp. 942-949
    • Maskey, R.P.1    Helmke, E.2    Laatsch, H.3
  • 51
    • 33846207996 scopus 로고    scopus 로고
    • Piperazimycins: cytotoxic hexadepsipeptides from a marine-derived bacterium of the genus Streptomyces
    • Miller E.D., Kauffman C.A., Jensen P.R., Fenical W. Piperazimycins: cytotoxic hexadepsipeptides from a marine-derived bacterium of the genus Streptomyces. J. Org. Chem. 2007, 72:323-330.
    • (2007) J. Org. Chem. , vol.72 , pp. 323-330
    • Miller, E.D.1    Kauffman, C.A.2    Jensen, P.R.3    Fenical, W.4
  • 52
    • 32044441838 scopus 로고    scopus 로고
    • Culture-dependent and culture-independent diversity within the obligate marine actinomycete genus Salinispora
    • Mincer T.J., Fenical W., Jensen P.R. Culture-dependent and culture-independent diversity within the obligate marine actinomycete genus Salinispora. Appl. Environ. Microbiol. 2005, 71:7019-7028.
    • (2005) Appl. Environ. Microbiol. , vol.71 , pp. 7019-7028
    • Mincer, T.J.1    Fenical, W.2    Jensen, P.R.3
  • 53
    • 0036795821 scopus 로고    scopus 로고
    • Widespread and persistent populations of a major new marine actinomycete taxon in ocean sediments
    • Mincer T.J., Jensen P.R., Kauffman C.A., Fenical W. Widespread and persistent populations of a major new marine actinomycete taxon in ocean sediments. Appl. Environ. Microbiol. 2002, 68:5005-5011.
    • (2002) Appl. Environ. Microbiol. , vol.68 , pp. 5005-5011
    • Mincer, T.J.1    Jensen, P.R.2    Kauffman, C.A.3    Fenical, W.4
  • 54
    • 4344701681 scopus 로고    scopus 로고
    • Aureoverticillactam, a novel 22-atom macrocyclic lactam from the marine actinomycete Streptomyces aureoverticillatus
    • Mitchell S.S., Nicholson B., Teisan S., Lam K.S., Barbara C. Aureoverticillactam, a novel 22-atom macrocyclic lactam from the marine actinomycete Streptomyces aureoverticillatus. J. Nat. Prod. 2004, 67:1400-1402.
    • (2004) J. Nat. Prod. , vol.67 , pp. 1400-1402
    • Mitchell, S.S.1    Nicholson, B.2    Teisan, S.3    Lam, K.S.4    Barbara, C.5
  • 56
    • 34247109045 scopus 로고    scopus 로고
    • Natural products as sources of new drugs over the last 25 years
    • Newman D.J., Cragg G.M. Natural products as sources of new drugs over the last 25 years. J. Nat. Prod. 2007, 70:461-477.
    • (2007) J. Nat. Prod. , vol.70 , pp. 461-477
    • Newman, D.J.1    Cragg, G.M.2
  • 57
    • 43249095424 scopus 로고    scopus 로고
    • Salinipyrones and pacificanones, mixed-precursor polyketides from the marine actinomycete Salinispora pacifica
    • Oh D.-C., Gontang E.A., Kauffman C.A., Jensen P.R., Fenical W. Salinipyrones and pacificanones, mixed-precursor polyketides from the marine actinomycete Salinispora pacifica. J. Nat. Prod. 2008, 71:570-575.
    • (2008) J. Nat. Prod. , vol.71 , pp. 570-575
    • Oh, D.-C.1    Gontang, E.A.2    Kauffman, C.A.3    Jensen, P.R.4    Fenical, W.5
  • 59
    • 0344830196 scopus 로고    scopus 로고
    • Thiocoraline, a novel depsipeptide with antitumor activity produced by a marine Micromonospora. II. Physico-chemical properties and structure determination
    • Perez B.J., Canedo L., Fernández P.J., Silva E.M. Thiocoraline, a novel depsipeptide with antitumor activity produced by a marine Micromonospora. II. Physico-chemical properties and structure determination. J. Antibiot. 1997, 50:738-741.
    • (1997) J. Antibiot. , vol.50 , pp. 738-741
    • Perez, B.J.1    Canedo, L.2    Fernández, P.J.3    Silva, E.M.4
  • 60
    • 22244465885 scopus 로고    scopus 로고
    • Synthesis of the fully functionalized core structure of the antibiotic abyssomicin C
    • Rath J.-P., Kinast S., Maier M.E. Synthesis of the fully functionalized core structure of the antibiotic abyssomicin C. Org. Lett. 2005, 7:3089-3092.
    • (2005) Org. Lett. , vol.7 , pp. 3089-3092
    • Rath, J.-P.1    Kinast, S.2    Maier, M.E.3
  • 63
    • 0030814840 scopus 로고    scopus 로고
    • Thiocoraline, a new depsipeptide with antitumor activity produced by a marine Micromonospora. I. Taxonomy, fermentation, isolation, and biological activities
    • Romero F., Espliego F., Pérez B.J., García d.Q.T., Grávalos D., De la Calle F., Fernández-Puentes J.L. Thiocoraline, a new depsipeptide with antitumor activity produced by a marine Micromonospora. I. Taxonomy, fermentation, isolation, and biological activities. J. Antibiot. 1997, 50:734-737.
    • (1997) J. Antibiot. , vol.50 , pp. 734-737
    • Romero, F.1    Espliego, F.2    Pérez, B.J.3    García, D.4    Grávalos, D.5    De la Calle, F.6    Fernández-Puentes, J.L.7
  • 65
    • 45549098717 scopus 로고    scopus 로고
    • Proximicins A, B, and C-antitumor furan analogues of netropsin from the marine actinomycete Verrucosispora induce upregulation of p53 and the cyclin kinase inhibitor p21
    • Schneider K., Keller S., Wolter F.E., Röglin L., Beil W., Seitz O., Nicholson G., Bruntner C., Riedlinger J., Fiedler H.-P. Proximicins A, B, and C-antitumor furan analogues of netropsin from the marine actinomycete Verrucosispora induce upregulation of p53 and the cyclin kinase inhibitor p21. Angew. Chem. Int. Ed. 2008, 47:3258-3261.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3258-3261
    • Schneider, K.1    Keller, S.2    Wolter, F.E.3    Röglin, L.4    Beil, W.5    Seitz, O.6    Nicholson, G.7    Bruntner, C.8    Riedlinger, J.9    Fiedler, H.-P.10
  • 66
    • 0141566386 scopus 로고    scopus 로고
    • Isolation and structure determination of an antimicrobial ester from a marine sediment-derived bacterium
    • Schumacher R.W., Talmage S.C., Miller S.A., Sarris K.E., Davidson B.S., Goldberg A. Isolation and structure determination of an antimicrobial ester from a marine sediment-derived bacterium. J. Nat. Prod. 2003, 66:1291-1293.
    • (2003) J. Nat. Prod. , vol.66 , pp. 1291-1293
    • Schumacher, R.W.1    Talmage, S.C.2    Miller, S.A.3    Sarris, K.E.4    Davidson, B.S.5    Goldberg, A.6
  • 67
    • 77958490163 scopus 로고    scopus 로고
    • Biologically active metabolites of marine actinobacteria
    • Sobolevskaya M., Kuznetsova T. Biologically active metabolites of marine actinobacteria. Russ. J. Bioorg. Chem. 2010, 36:560-573.
    • (2010) Russ. J. Bioorg. Chem. , vol.36 , pp. 560-573
    • Sobolevskaya, M.1    Kuznetsova, T.2
  • 68
    • 14744287528 scopus 로고    scopus 로고
    • Estimating and comparing the diversity of marine actinobacteria
    • Stach E., Bull A.T. Estimating and comparing the diversity of marine actinobacteria. Antonie Van Leeuwenhoek 2005, 87:3-9.
    • (2005) Antonie Van Leeuwenhoek , vol.87 , pp. 3-9
    • Stach, E.1    Bull, A.T.2
  • 69
    • 0034887171 scopus 로고    scopus 로고
    • Polyketide biosynthesis: a millennium review
    • Staunton J., Weissman K.J. Polyketide biosynthesis: a millennium review. Nat. Prod. Rep. 2001, 18:380-416.
    • (2001) Nat. Prod. Rep. , vol.18 , pp. 380-416
    • Staunton, J.1    Weissman, K.J.2
  • 71
    • 0024404622 scopus 로고
    • Altemicidin, a new acaricidal and antitumor substance. I. Taxonomy, fermentation, isolation and physico-chemical and biological properties
    • Takahashi A., Kurasawa S., Ikeda D., Okami Y., Takeuchi T. Altemicidin, a new acaricidal and antitumor substance. I. Taxonomy, fermentation, isolation and physico-chemical and biological properties. J. Antibiot. 1989, 42:1556-1561.
    • (1989) J. Antibiot. , vol.42 , pp. 1556-1561
    • Takahashi, A.1    Kurasawa, S.2    Ikeda, D.3    Okami, Y.4    Takeuchi, T.5
  • 72
    • 0036373085 scopus 로고    scopus 로고
    • Integrated approach to explore the potential of marine microorganisms for the production of bioactive metabolites, tools and applications of biochemical engineering science
    • Wagner-Döbler I., Beil W., Lang S., Meiners M., Laatsch H. Integrated approach to explore the potential of marine microorganisms for the production of bioactive metabolites, tools and applications of biochemical engineering science. Adv. Biochem. Eng. Biotechnol. 2002, 74:207-238.
    • (2002) Adv. Biochem. Eng. Biotechnol. , vol.74 , pp. 207-238
    • Wagner-Döbler, I.1    Beil, W.2    Lang, S.3    Meiners, M.4    Laatsch, H.5
  • 73
    • 0345550239 scopus 로고    scopus 로고
    • Exploiting the genetic potential of polyketide producing streptomycetes
    • Weber T., Welzel K., Pelzer S., Vente A., Wohlleben W. Exploiting the genetic potential of polyketide producing streptomycetes. J. Biotechnol. 2003, 106:221-232.
    • (2003) J. Biotechnol. , vol.106 , pp. 221-232
    • Weber, T.1    Welzel, K.2    Pelzer, S.3    Vente, A.4    Wohlleben, W.5
  • 75
    • 34447299920 scopus 로고    scopus 로고
    • Arenicolides AC, 26-membered ring macrolides from the marine actinomycete Salinispora arenicola
    • Williams P.G., Miller E.D., Asolkar R.N., Jensen P.R., Fenical W. Arenicolides AC, 26-membered ring macrolides from the marine actinomycete Salinispora arenicola. J. Org. Chem. 2007, 72:5025-5034.
    • (2007) J. Org. Chem. , vol.72 , pp. 5025-5034
    • Williams, P.G.1    Miller, E.D.2    Asolkar, R.N.3    Jensen, P.R.4    Fenical, W.5
  • 76
    • 33746872952 scopus 로고    scopus 로고
    • N-Carboxamido-staurosporine and Selina-4 (14), 7 (11)-diene-8, 9-diol, new metabolites from a marine Streptomyces sp.
    • Wu S.J., Fotso S., Li F., Qin S., Kelter G., Fiebig H.H., Laatsch H. N-Carboxamido-staurosporine and Selina-4 (14), 7 (11)-diene-8, 9-diol, new metabolites from a marine Streptomyces sp. J. Antibiot. 2006, 59:331-337.
    • (2006) J. Antibiot. , vol.59 , pp. 331-337
    • Wu, S.J.1    Fotso, S.2    Li, F.3    Qin, S.4    Kelter, G.5    Fiebig, H.H.6    Laatsch, H.7
  • 77
    • 33947367714 scopus 로고    scopus 로고
    • Amorphane sesquiterpenes from a marine Streptomyces sp.
    • Wu S.J., Fotso S., Li F., Qin S., Laatsch H. Amorphane sesquiterpenes from a marine Streptomyces sp. J. Nat. Prod. 2007, 70:304-306.
    • (2007) J. Nat. Prod. , vol.70 , pp. 304-306
    • Wu, S.J.1    Fotso, S.2    Li, F.3    Qin, S.4    Laatsch, H.5
  • 78
    • 19544376849 scopus 로고    scopus 로고
    • Biosynthesis of the antitumor agent Chartreusin involves the oxidative rearrangement of an anthracyclic polyketide
    • Xu Z., Jakobi K., Welzel K., Hertweck C. Biosynthesis of the antitumor agent Chartreusin involves the oxidative rearrangement of an anthracyclic polyketide. Chem. Biol. 2005, 12:579-588.
    • (2005) Chem. Biol. , vol.12 , pp. 579-588
    • Xu, Z.1    Jakobi, K.2    Welzel, K.3    Hertweck, C.4
  • 79
    • 1642561022 scopus 로고    scopus 로고
    • Aburatubolactams and zoanthamines, naturally occurring bioactive alkaloids
    • Yamada K., Kuramoto M., Uemura D. Aburatubolactams and zoanthamines, naturally occurring bioactive alkaloids. Recent Res. Dev. Pure Appl. Chem. 1999, 3:245-254.
    • (1999) Recent Res. Dev. Pure Appl. Chem. , vol.3 , pp. 245-254
    • Yamada, K.1    Kuramoto, M.2    Uemura, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.