Biochemistry

Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 9 No. 3, Special Issue, 2006
© 2006 by Pontificia Universidad Católica de Valparaíso -- Chile  
DOI: 10.2225/vol9-issue3-fulltext-4  
RESEARCH ARTICLE

Morphological and chemical diversity in the Type IV glandular trichomes of Solananeae (S. sisymbrifolium and N. glauca) as germplasm resources for agricultural and food uses

Verónica Cesio
Departamento de Química Orgánica
Facultad de Química
Universidad de la República
Avda. General Flores 2124
Montevideo, Uruguay
Tel: 924 40 68
Fax: 924 19 06
E-mail: cs@fq.edu.uy

Carmelo Dutra
Departamento de Química Orgánica
Facultad de Química
Universidad de la República
Avda. General Flores 2124
Montevideo, Uruguay
Tel: 924 40 68
Fax: 924 19 06
E-mail: cdutra@fq.edu.uy

Patrick Moyna
Departamento de Química Orgánica
Facultad de Química
Universidad de la República
Avda. General Flores 2124
Montevideo, Uruguay
Tel: 924 40 68
Fax: 924 19 06
E-mail: pmoyna@fq.edu.uy

Horacio Heinzen*
Departamento de Química Orgánica
Facultad de Química
Universidad de la República
Avda. General Flores 2124
Montevideo, Uruguay
Tel: 924 40 68
Fax: 924 19 06
E-mail: heinzen@fq.edu.uy

*Corresponding author

Financial support: CSIC Nº203 and CONICYT Nº122.

Keywords: antifungic activity, interespecies variability, mycotoxins, sugar esters.

Abbreviations:

CC: column chromatography
GC-MS-EI: gas chromatography - mass spectrometry - electronic impact
MALDI-TOF: Matrix Assisted Laser Desorption Ionization-Time of Flight
Ng: Nicotiana glauca
NMR: Nuclear Magnetic Resonance
SE: sugar esters
SEM: Scanning Electron Microscopy
Ss: Solanum sisymbrifolium

Abstract
Reprint (PDF)

Morphological variation in type IV trichomes in Ss and Ng was studied through SEM. The differences can be related to chemical differences in the excreted sugar esters. Ng trichomes exude two fractions, one of glucose tri-esters and the other one of sucrose tetra-esters, in a 3:7 ratio. The main acid found forming these esthers, is 3-methylvalerianic acid, in consonance to those secreted by other Solanaceae. Esters from Ss are novel structures, which can also be separated into three fractions, two of arabinoxylans, and the other one of arabinose, all glycosilated with β-hydroxipalmitic acid and sterified with the C12-C16 acids. All five fractions have antifungic activity at μg/cm2 concentrations, both against common and mycotoxigenic fungi, such as A. niger, A. flavus, P. chrysogenum y P. expansum. A. flavus does not grow in the presence of the SE of Ss and is not insensible to those from Ng, but these last are more effective in the inhibition of P. expansum, the other mycotoxigenic fungi studied. The differential antifungal activity observed gives the plant protection against a wide spectrum of fungi, resulting in a better adaptation to the environment. Both plants are common weeds, with the potential of contributing to germplams lines in the improvement programmes of crops such as L. esculentum, and their extracts can be used as natural fungicides to protect crops and plantations.

 
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