Chaetoglocins A-D, four new metabolites from the endophytic fungus Chaetomium globosum

Planta Medica

Volumn 77, Issue 3, 2011, Pages 277-280

  Ge, Hui Ming ^a   Zhang, Qiang ^a   Xu, Su Hai ^a   Guo, Zhi Kai ^a   Song, Yong Chun ^a   Huang, Wu Yang ^a   Tan, Ren Xiang ^a  

^a NANJING UNIVERSITY   (China)

Author keywords

antibiotic; Chaetomiaceae; Chaetomium globosum; endophyte; secondary metabolites

Indexed keywords

CHAETOGLOCIN A; CHAETOGLOCIN B; CHAETOGLOCIN C; CHAETOGLOCIN D; KANAMYCIN; NATURAL PRODUCT; TETRACYCLINE; UNCLASSIFIED DRUG;

ANTIMICROBIAL ACTIVITY; ARTICLE; BACILLUS SUBTILIS; BERMUDA GRASS; CARBON NUCLEAR MAGNETIC RESONANCE; CHAETOMIUM GLOBOSUM; CONTROLLED STUDY; CYNODON; DRUG ISOLATION; ESCHERICHIA COLI; FERMENTATION; FUNGUS; FUNGUS CULTURE; GRAM POSITIVE BACTERIUM; HETERONUCLEAR MULTIPLE BOND CORRELATION; INFRARED SPECTROSCOPY; METABOLITE; MICROCOCCUS LUTEUS; MINIMUM INHIBITORY CONCENTRATION; MYCOBACTERIUM SMEGMATIS; NONHUMAN; PLANT ROOT; PROTON NUCLEAR MAGNETIC RESONANCE; PSEUDOMONAS AERUGINOSA; STREPTOCOCCUS PYOGENES; STRUCTURE ACTIVITY RELATION; ULTRAVIOLET SPECTROSCOPY;

ANTI-BACTERIAL AGENTS; BIOLOGICAL PRODUCTS; CHAETOMIUM; CYNODON; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; MYCORRHIZAE;

CHAETOMIACEAE; CHAETOMIUM GLOBOSUM; CYNODON DACTYLON; FUNGI; POSIBACTERIA;

EID: 79551685409     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0030-1250292     Document Type: Article

References (20)

1. Miglia K J., McArthur E D., Redman R S., Rodriguez R J., Zak J C., Freeman D C. Genotype, soil type, and locale effects on reciprocal transplant vigor, endophyte growth, and microbial functional diversity of a narrow sagebrush hybrid zone in Salt Cre (Pubitemid 46955017)
2. Zhang H W., Song Y C., Tan R X. Biology and chemistry of endophytes. Nat Prod Rep 2006 23 753-771 (Pubitemid 44455389)
3. Strobel G, Daisy B, Castillo U, Harper J. Natural products from endophytic microorganisms. J Nat Prod 2004 67 257-268 (Pubitemid 38282917)
4. Gunatilaka A. Natural products from plant-associated microorganisms: distribution, structural diversity, bioactivity, and implications of their occurrence. J Nat Prod 2006 69 509-526
5. Von Arx J A., Guarro J, Figueras M J. The ascomycetes genus Chaetomium. Nova Hedwigia Beih 1986 84 1-162
6. Schmann J, Hertweck C. Molecular basis of cytochalasan biosynthesis in fungi: gene cluster analysis and evidence for the involvement of a PKS-NRPS hybrid synthase by RNA silencing. J Am Chem Soc 2007 129 9564-9565 (Pubitemid 47237448)
7. Ge H M., Zhang W Y., Ding G, Saparpakorn P, Song Y C., Hannongbua S, Tan R X. Chaetoglobins A and B, two unusual alkaloids from endophytic Chaetomium globosum culture. Chem Commun 2008 45 5978-5980
8. Jiao R H., Xu S, Liu J Y., Ge H M., Ding H, Xu C, Zhu H L., Tan R X. Chaetominine, a cytotoxic alkaloid produced by endophytic Chaetomium sp. IFB-E015. Org Lett 2006 8 5709-5712
9. Ding G, Song Y C., Chen J R., Xu C, Ge H M., Wang X T., Tan R X. Chaetoglobosin U, a cytochalasan alkaloid from endophyte Chaetomium globosum IFB-E019. J Nat Prod 2006 69 302-304
10. Urones J G., Marcos I S., Basabe P, Diez D, Garrido N M., Alonso C, Oliva I M., Lithgow A M., Moro R F., Sexmero M J., Lopez C. Compounds with the labdane skeleton from Halimium viscosum. Phytochemistry 1994 35 713-719 (Pubitemid 2044238)
11. Hernández-Hernández J D., Román-Marín L U., Cerda-García-Rojas C M., Joseph-Nathan P. Verticillane derivatives from Bursera suntui and Bursera kerberi. J Nat Prod 2005 68 1598-1602 (Pubitemid 41789564)
12. Huo J, Yang S P., Ding J, Yue J M. Cytotoxic sesquiterpene lactones from Eupatorium lindleyanum. J Nat Prod 2004 67 1470-1475 (Pubitemid 39298612)
13. Suárez-Gómez B, Souto M L., Cruz P G., Fernández J J., Norte M. New targets in diarrhetic shellfish poisoning control. J Nat Prod 2005 68 596-599 (Pubitemid 40586328)
14. Gao F, Mabry T J. Ten cis-clerodane-type diterpene lactones from Gutierrezia texana. Phytochemistry 1987 26 209-216
15. Niedermeyer T H., Lindequist U, Mentel R, Gordes D, Schmidt E, Thurow K, Lalk M. Antiviral terpenoid constituents of Ganoderma pfeifferi. J Nat Prod 2005 68 1728-1731 (Pubitemid 43082643)
16. Pagani A, Navarrete C, Fiebich B L., Munoz E, Appendino G. Synthesis and biological evaluation of 12-aminoacylphorboids. J Nat Prod 2010 73 447-451
17. Kim T H., Ito H, Hatano T, Hasegawa T, Akiba A, Machiguchi T, Yoshida T. Bisabolane- and santalane-type sesquiterpenoids from Santalum album of Indian origin. J Nat Prod 2005 68 1805-1808 (Pubitemid 43082662)
18. 13C chemical shifts produced by oxygen atoms at the c position by quantum chemistry calculations. J Mol Struct 2009 919 290-294
19. Ge H M., Shen Y, Zhu C H., Tan S H., Ding H, Song Y C., Tan R X. Penicidones A-C, three cytotoxic alkaloidal metabolites of an endophytic Penicillium sp. Phytochemistry 2008 69 571-576
20. National Committee for Clinical Laboratory Standards (NCCLS). Methods for dilution in antimicrobial susceptibility tests: approved standard M2-A5. Villanova National Committee for Clinical Laboratory Standards 1993