A new chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) affects Soybean Asian rust (<it>Phakopsora pachyrhizi</it>) spore germination

<p>Abstract</p> <p>Background</p> <p>Asian rust (<it>Phakopsora pachyrhizi</it>) 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 x...

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Main Authors: Mehta Angela, Filho Edivaldo XF, Fitches Elaine, Price Daniel, Oliveira-Neto Osmundo B, Silva Marilia S, Moreira Leonora RS, Seixas Claudine DS, Godoy Claudia V, Santana Celso G, Vasconcelos Erico AR, Gatehouse John A, Grossi-De-Sa Maria F
Format: Article
Language:English
Published: BMC 2011-02-01
Series:BMC Biotechnology
Online Access:http://www.biomedcentral.com/1472-6750/11/14
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spelling doaj-d5afbfc0fd9f4ed78a915c85d37fb2422020-11-25T03:48:50ZengBMCBMC Biotechnology1472-67502011-02-011111410.1186/1472-6750-11-14A new chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) affects Soybean Asian rust (<it>Phakopsora pachyrhizi</it>) spore germinationMehta AngelaFilho Edivaldo XFFitches ElainePrice DanielOliveira-Neto Osmundo BSilva Marilia SMoreira Leonora RSSeixas Claudine DSGodoy Claudia VSantana Celso GVasconcelos Erico ARGatehouse John AGrossi-De-Sa Maria F<p>Abstract</p> <p>Background</p> <p>Asian rust (<it>Phakopsora pachyrhizi</it>) 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 (<it>Coffea arabica</it>) (CaclXIP) leaves was cloned into the pGAPZα-B vector for expression in <it>Pichia pastoris</it>.</p> <p>Results</p> <p>A cDNA encoding a chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) (CaclXIP), was isolated from leaves. The amino acid sequence predicts a (β/α)<sub>8 </sub>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 <it>Pichia pastoris</it>. Enzymatic assay showed that purified recombinant CaclXIP had only residual chitinolytic activity. However, it inhibited xylanases from <it>Acrophialophora nainiana </it>by approx. 60% when present at 12:1 (w/w) enzyme:inhibitor ratio. Additionally, CaclXIP at 1.5 μg/μL inhibited the germination of spores of <it>Phakopsora pachyrhizi </it>by 45%.</p> <p>Conclusions</p> <p>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.</p> http://www.biomedcentral.com/1472-6750/11/14
collection DOAJ
language English
format Article
sources DOAJ
author Mehta Angela
Filho Edivaldo XF
Fitches Elaine
Price Daniel
Oliveira-Neto Osmundo B
Silva Marilia S
Moreira Leonora RS
Seixas Claudine DS
Godoy Claudia V
Santana Celso G
Vasconcelos Erico AR
Gatehouse John A
Grossi-De-Sa Maria F
spellingShingle Mehta Angela
Filho Edivaldo XF
Fitches Elaine
Price Daniel
Oliveira-Neto Osmundo B
Silva Marilia S
Moreira Leonora RS
Seixas Claudine DS
Godoy Claudia V
Santana Celso G
Vasconcelos Erico AR
Gatehouse John A
Grossi-De-Sa Maria F
A new chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) affects Soybean Asian rust (<it>Phakopsora pachyrhizi</it>) spore germination
BMC Biotechnology
author_facet Mehta Angela
Filho Edivaldo XF
Fitches Elaine
Price Daniel
Oliveira-Neto Osmundo B
Silva Marilia S
Moreira Leonora RS
Seixas Claudine DS
Godoy Claudia V
Santana Celso G
Vasconcelos Erico AR
Gatehouse John A
Grossi-De-Sa Maria F
author_sort Mehta Angela
title A new chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) affects Soybean Asian rust (<it>Phakopsora pachyrhizi</it>) spore germination
title_short A new chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) affects Soybean Asian rust (<it>Phakopsora pachyrhizi</it>) spore germination
title_full A new chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) affects Soybean Asian rust (<it>Phakopsora pachyrhizi</it>) spore germination
title_fullStr A new chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) affects Soybean Asian rust (<it>Phakopsora pachyrhizi</it>) spore germination
title_full_unstemmed A new chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) affects Soybean Asian rust (<it>Phakopsora pachyrhizi</it>) spore germination
title_sort new chitinase-like xylanase inhibitor protein (xip) from coffee (<it>coffea arabica</it>) affects soybean asian rust (<it>phakopsora pachyrhizi</it>) spore germination
publisher BMC
series BMC Biotechnology
issn 1472-6750
publishDate 2011-02-01
description <p>Abstract</p> <p>Background</p> <p>Asian rust (<it>Phakopsora pachyrhizi</it>) 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 (<it>Coffea arabica</it>) (CaclXIP) leaves was cloned into the pGAPZα-B vector for expression in <it>Pichia pastoris</it>.</p> <p>Results</p> <p>A cDNA encoding a chitinase-like xylanase inhibitor protein (XIP) from coffee (<it>Coffea arabica</it>) (CaclXIP), was isolated from leaves. The amino acid sequence predicts a (β/α)<sub>8 </sub>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 <it>Pichia pastoris</it>. Enzymatic assay showed that purified recombinant CaclXIP had only residual chitinolytic activity. However, it inhibited xylanases from <it>Acrophialophora nainiana </it>by approx. 60% when present at 12:1 (w/w) enzyme:inhibitor ratio. Additionally, CaclXIP at 1.5 μg/μL inhibited the germination of spores of <it>Phakopsora pachyrhizi </it>by 45%.</p> <p>Conclusions</p> <p>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.</p>
url http://www.biomedcentral.com/1472-6750/11/14
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