Osmotin from Calotropis procera latex: New insights into structure and antifungal properties
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2011
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Resumo |
This study aimed at investigating the structural properties and mechanisms of the antifungal action of CpOsm, a purified osmotin from Calotropis procera latex. Fluorescence and CD assays revealed that the CpOsm structure is highly stable, regardless of pH levels. Accordingly, CpOsm inhibited the spore germination of Fusarium solani in all pH ranges tested. The content of the secondary structure of CpOsm was estimated as follows: alpha-helix (20%), beta-sheet (33%), turned (19%) and unordered (28%). RMSD 1%. CpOsm was stable at up to 75 degrees C, and thermal denaturation (T(m)) was calculated to be 77.8 degrees C. This osmotin interacted with the negatively charged large unilamellar vesicles (LUVs) of 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-rac-1-glycerol (POPG), inducing vesicle permeabilization by the leakage of calcein. CpOsm induced the membrane permeabilization of spores and hyphae from Fusarium solani, allowing for propidium iodide uptake. These results show that CpOsm is a stable protein, and its antifungal activity involves membrane permeabilization, as property reported earlier for other osmotins and thaumatin-like proteins. (C) 2011 Elsevier B.V. All rights reserved. Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico (FUNCAP) FUNCAP CNPq (Universal, RENORBIO and Brazil/India cooperation) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) IFS IFS |
Identificador |
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, v.1808, n.10, p.2501-2507, 2011 0005-2736 http://producao.usp.br/handle/BDPI/30073 10.1016/j.bbamem.2011.07.014 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE BV |
Relação |
Biochimica Et Biophysica Acta-biomembranes |
Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE BV |
Palavras-Chave | #Calcein #Fusarium solani #Laticifer protein #Propidium iodide #Thaumatin-like protein #THAUMATIN-LIKE PROTEINS #CRYSTAL-STRUCTURE #ANTIMICROBIAL PEPTIDES #CIRCULAR-DICHROISM #MOLECULAR-CLONING #PR-5 PROTEIN #PLANTS #FLUORESCENCE #Biochemistry & Molecular Biology #Biophysics |
Tipo |
article original article publishedVersion |