Co-Production of bisphenylpropanoid amides and meroterpenes by an endophytic Penicillium brasilianum found in the root bark of Melia azedarach

Zeitschrift fur Naturforschung - Section C Journal of Biosciences

Volumn 64, Issue 5-6, 2009, Pages 355-360

  Fill, Taicia P ^a   dos Santos, Regina M Geris ^b   Barisson, Anderson ^c   Rodrigues Filho, Edson ^a   Souza, Antonia Q L ^d  

^a FEDERAL UNIVERSITY OF SÃO CARLOS   (Brazil)

^b FEDERAL UNIVERSITY OF BAHIA   (Brazil)

^c FEDERAL UNIVERSITY OF AMAZONAS   (Brazil)

^d FEDERAL UNIVERSITY OF PARANÁ   (Brazil)

Author keywords

Bisphenylpropanoid; Brasiliamide; Melia azedarach; Penicillium brasilianum

Indexed keywords

BACTERIA (MICROORGANISMS); FUNGI; MELIA AZEDARACH; MELIACEAE; PENICILLIUM; PENICILLIUM BRASILIANUM;

1,3 DIOXOLANE DERIVATIVE; FUNGAL DNA; PHENYLALANINE; RIBOSOME DNA;

ARTICLE; CHEMISTRY; GENETICS; ISOLATION AND PURIFICATION; MELIA AZEDARACH; METABOLISM; METHODOLOGY; MICROBIOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PENICILLIUM; PLANT ROOT; PLANT STEM; RICE;

DIOXOLES; DNA, FUNGAL; DNA, RIBOSOMAL; MAGNETIC RESONANCE SPECTROSCOPY; MELIA AZEDARACH; ORYZA SATIVA; PENICILLIUM; PHENYLALANINE; PLANT ROOTS; PLANT STEMS;

EID: 70349331694     PISSN: 09395075     EISSN: None     Source Type: Journal    
DOI: 10.1515/znc-2009-5-609     Document Type: Article

References (15)

1. Chittari P., Jadhev V. R., Ganesh K. N., and Rajappa S. (1998), Synthesis and metal complexation of chiral 3-mono-or 3,3-bis-allyl-2-hydroxypyrrolopyrazine-1,4-diones. J. Chem. Soc. Perkin Trans. 1, 1319-1324.
2. Essemberg M. (2001), Prospects for strengthening plant defenses through phytoalexin engineering. Physiol. Mol. Plant. Pathol. 59, 71-81.
3. Ferrer J. L., Austin M. B., Stewart C., and Noel J. P. (2008), Structure and function of enzymes involved in the biosynthesis of phenylpropanoids. Plant Physiol. Biochem. 46, 356-370.
4. Fill T. P., Santos R. M. G., and Rodrigues-Filho E. (2007), Four additional meroterpenes produced by Penicillium sp. found in association with Melia azedarach. Possible biosynthetic intermediates to austin. Z. Naturforsch. 62b, 1035-1044.
5. Fujita T. and Hayashi H. (2004), New brasiliamide congeners, brasiliamides C, D and E, from Penicillium brasilianum Batista JV-379. Biosci. Biotechnol. Biochem. 68, 820-826.
6. Fujita T., Makishima D., Akiyama K., and Hayashi H. (2002), New convulsive compounds, brasiliamides A and B, from Penicillium brasilianum Batista JV-379. Biosci. Biotechnol. Biochem. 66, 1697-1705.
7. Hirsch S., Miroz A., McCarthy P., and Kashman Y. (1989), Etzionin, a new antifungal metabolite from a red sea tunicate. Tetrahedron Lett. 30, 4291-4294.
8. Petrini O., Sieber T. N., Toti L., and Viret O. (1992), Ecology, metabolite production and substrate utilization in endophytic fungi. Nat. Toxins 1, 185-196.
9. Santos R. M. G. and Rodrigues-Filho E. (2002), Meroterpenes from Penicillium sp. found in association with Melia azedarach. Phytochemistry 61, 907-912.
10. Santos R. M. G. and Rodrigues-Filho E. (2003a), Structures of meroterpenes produced by Penicillium sp., an endophytic fungus found associated with Melia azedarach. J. Braz. Chem. Soc. 14, 722-727.
11. Santos R.M.G. and Rodrigues-Filho E. (2003b), Further meroterpenes produced by Penicillium sp., an endophyte obtained from Melia azedarach. Z. Naturforsch. 58c, 663-669.
12. Santos R. M. G. and Rodrigues-Filho E. (2004), Análise de padrões de meroterpenos por cromatografia líquida acoplada a espectrometria de massas LC/ESI-MS/ MS. LabCiencia Not. Tec. Lab. 3, 12-14.
13. Santos R. M. G., Rodrigues-Filho E., Rocha W. C., and Teixeira M. F. S. (2003), Endophytic fungi from Me-lia azedarach. World J. Microbiol. Biotechnol. 19, 767-770.
14. Seshime Y., Juvvadi P. R., Fuji I., and Kitamoto K. (2005a), Discovery of a novel superfamily of type III polyketide synthases in Aspergillus oryzae. Biochem. Biophys. Res. Commun. 331, 253-260.
15. Seshime Y., Juvvadi P. R., Fuji I., and Kitamoto K. (2005b), Genomic evidences for the existence of a phenylpropanoid metabolic pathway in Aspergillus oryzae. Biochem. Biophys. Res. Commun. 337, 747-751.