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Overexpression of an Acidic Endo-β-1,3-1,4-glucanase in Transgenic Maize Seed for Direct Utilization in Animal Feed

BACKGROUND: Incorporation of exogenous glucanase into animal feed is common practice to remove glucan, one of the anti-nutritional factors, for efficient nutrition absorption. The acidic endo-β-1,3-1,4-glucanase (Bgl7A) from Bispora sp. MEY-1 has excellent properties and represents a potential enzym...

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Autores principales: Zhang, Yuhong, Xu, Xiaolu, Zhou, Xiaojin, Chen, Rumei, Yang, Peilong, Meng, Qingchang, Meng, Kun, Luo, Huiying, Yuan, Jianhua, Yao, Bin, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876984/
https://www.ncbi.nlm.nih.gov/pubmed/24391711
http://dx.doi.org/10.1371/journal.pone.0081993
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author Zhang, Yuhong
Xu, Xiaolu
Zhou, Xiaojin
Chen, Rumei
Yang, Peilong
Meng, Qingchang
Meng, Kun
Luo, Huiying
Yuan, Jianhua
Yao, Bin
Zhang, Wei
author_facet Zhang, Yuhong
Xu, Xiaolu
Zhou, Xiaojin
Chen, Rumei
Yang, Peilong
Meng, Qingchang
Meng, Kun
Luo, Huiying
Yuan, Jianhua
Yao, Bin
Zhang, Wei
author_sort Zhang, Yuhong
collection PubMed
description BACKGROUND: Incorporation of exogenous glucanase into animal feed is common practice to remove glucan, one of the anti-nutritional factors, for efficient nutrition absorption. The acidic endo-β-1,3-1,4-glucanase (Bgl7A) from Bispora sp. MEY-1 has excellent properties and represents a potential enzyme supplement to animal feed. METHODOLOGY/PRINCIPAL FINDINGS: Here we successfully developed a transgenic maize producing a high level of Bgl7AM (codon modified Bgl7A) by constructing a recombinant vector driven by the embryo-specific promoter ZM-leg1A. Southern and Western blot analysis indicated the stable integration and specific expression of the transgene in maize seeds over four generations. The β-glucanase activity of the transgenic maize seeds reached up to 779,800 U/kg, about 236-fold higher than that of non-transgenic maize. The β-glucanase derived from the transgenic maize seeds had an optimal pH of 4.0 and was stable at pH 1.0–8.0, which is in agreement with the normal environment of digestive tract. CONCLUSION/SIGNIFICANCE: Our study offers a transgenic maize line that could be directly used in animal feed without any glucanase production, purification and supplementation, consequently simplifying the feed enzyme processing procedure.
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spelling pubmed-38769842014-01-03 Overexpression of an Acidic Endo-β-1,3-1,4-glucanase in Transgenic Maize Seed for Direct Utilization in Animal Feed Zhang, Yuhong Xu, Xiaolu Zhou, Xiaojin Chen, Rumei Yang, Peilong Meng, Qingchang Meng, Kun Luo, Huiying Yuan, Jianhua Yao, Bin Zhang, Wei PLoS One Research Article BACKGROUND: Incorporation of exogenous glucanase into animal feed is common practice to remove glucan, one of the anti-nutritional factors, for efficient nutrition absorption. The acidic endo-β-1,3-1,4-glucanase (Bgl7A) from Bispora sp. MEY-1 has excellent properties and represents a potential enzyme supplement to animal feed. METHODOLOGY/PRINCIPAL FINDINGS: Here we successfully developed a transgenic maize producing a high level of Bgl7AM (codon modified Bgl7A) by constructing a recombinant vector driven by the embryo-specific promoter ZM-leg1A. Southern and Western blot analysis indicated the stable integration and specific expression of the transgene in maize seeds over four generations. The β-glucanase activity of the transgenic maize seeds reached up to 779,800 U/kg, about 236-fold higher than that of non-transgenic maize. The β-glucanase derived from the transgenic maize seeds had an optimal pH of 4.0 and was stable at pH 1.0–8.0, which is in agreement with the normal environment of digestive tract. CONCLUSION/SIGNIFICANCE: Our study offers a transgenic maize line that could be directly used in animal feed without any glucanase production, purification and supplementation, consequently simplifying the feed enzyme processing procedure. Public Library of Science 2013-12-31 /pmc/articles/PMC3876984/ /pubmed/24391711 http://dx.doi.org/10.1371/journal.pone.0081993 Text en © 2013 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Yuhong
Xu, Xiaolu
Zhou, Xiaojin
Chen, Rumei
Yang, Peilong
Meng, Qingchang
Meng, Kun
Luo, Huiying
Yuan, Jianhua
Yao, Bin
Zhang, Wei
Overexpression of an Acidic Endo-β-1,3-1,4-glucanase in Transgenic Maize Seed for Direct Utilization in Animal Feed
title Overexpression of an Acidic Endo-β-1,3-1,4-glucanase in Transgenic Maize Seed for Direct Utilization in Animal Feed
title_full Overexpression of an Acidic Endo-β-1,3-1,4-glucanase in Transgenic Maize Seed for Direct Utilization in Animal Feed
title_fullStr Overexpression of an Acidic Endo-β-1,3-1,4-glucanase in Transgenic Maize Seed for Direct Utilization in Animal Feed
title_full_unstemmed Overexpression of an Acidic Endo-β-1,3-1,4-glucanase in Transgenic Maize Seed for Direct Utilization in Animal Feed
title_short Overexpression of an Acidic Endo-β-1,3-1,4-glucanase in Transgenic Maize Seed for Direct Utilization in Animal Feed
title_sort overexpression of an acidic endo-β-1,3-1,4-glucanase in transgenic maize seed for direct utilization in animal feed
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876984/
https://www.ncbi.nlm.nih.gov/pubmed/24391711
http://dx.doi.org/10.1371/journal.pone.0081993
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