Title:	A new chitinase-like xylanase inhibitor protein (XIP) from coffee (Coffea arabica) affects Soybean Asian rust (Phakopsora pachyrhizi) spore germination.
Authors:	VASCONCELOS, E. A. R. SANTANA, C. G. GODOY, C. V. SEIXAS, C. D. S. SILVA, M. S. MOREIRA, L. R. S. OLIVEIRA-NETO, O. B. PRICE, D. FITCHES, E. FERREIRA FILHO, E. X. MEHTA, A. GATEHOUSE, J. A. GROSSI-DE-SA, M. F.
Affiliation:	ERICO A. R. VASCONCELOS CELSO G. SANTANA CLAUDIA VIEIRA GODOY, CNPSO CLAUDINE DINALI SANTOS SEIXAS, CNPSO MARILIA SANTOS SILVA, CPAC LEONORA R. S. MOREIRA, UNIVERSIDADE DE BRASÍLIA OSMUNDO B. OLIVEIRA-NETO DANIEL PRICE, DURHAM UNIVERSITY ELAINE FITCHES, DURHAM UNIVERSITY EDIVALDO X. FERREIRA FILHO, UNIVERSIDADE DE BRASÍLIA ANGELA MEHTA DOS REIS, CENARGEN JOHN A. GATEHOUSE, UNIVERSITY DURHAM MARIA FATIMA GROSSI DE SA, CENARGEN.
Date Issued:	2011
Citation:	BMC Biotechnology, v. 11, 2011.
Description:	Background: Asian rust (Phakopsora pachyrhizi) is a common disease in Brazilian soybean fields and it is difficult to control. To identify a biochemical candidate with potential to combat this disease, a new chitinase-like xylanase inhibitor protein (XIP) from coffee (Coffea arabica) (CaclXIP) leaves was cloned into the pGAPZa-B vector for expression in Pichia pastoris. Results: A cDNA encoding a chitinase-like xylanase inhibitor protein (XIP) from coffee (Coffea arabica) (CaclXIP), was isolated from leaves. The amino acid sequence predicts a (b/a)8 topology common to Class III Chitinases (glycoside hydrolase family 18 proteins; GH18), and shares similarity with other GH18 members, although it lacks the glutamic acid residue essential for catalysis, which is replaced by glutamine. CaclXIP was expressed as a recombinant protein in Pichia pastoris. Enzymatic assay showed that purified recombinant CaclXIP had only residual chitinolytic activity. However, it inhibited xylanases from Acrophialophora nainiana by approx. 60% when present at 12:1 (w/w) enzyme:inhibitor ratio. Additionally, CaclXIP at 1.5 ?g/?L inhibited the germination of spores of Phakopsora pachyrhizi by 45%. Conclusions: Our data suggests that CaclXIP belongs to a class of naturally inactive chitinases that have evolved to act in plant cell defence as xylanase inhibitors. Its role on inhibiting germination of fungal spores makes it an eligible candidate gene for the control of Asian rust.
Thesagro:	Praga de Planta Soja
Keywords:	Controle de praga
DOI:	https://www.doi.org/10.1186/1472-6750-11-14
Type of Material:	Artigo de periódico
Access:	openAccess
Appears in Collections:	Artigo em periódico indexado (CPAC)