Cargando…

Production of a Highly Protease-Resistant Fungal α-Galactosidase in Transgenic Maize Seeds for Simplified Feed Processing

Raffinose-family oligosaccharide (RFO) in soybeans is one of the major anti-nutritional factors for poultry and livestocks. α-Galactosidase is commonly supplemented into the animal feed to hydrolyze α-1,6-galactosidic bonds on the RFOs. To simplify the feed processing, a protease-resistant α-galacto...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Wenxia, Zhang, Yuhong, Zhou, Xiaojin, Zhang, Wei, Xu, Xiaolu, Chen, Rumei, Meng, Qingchang, Yuan, Jianhua, Yang, Peilong, Yao, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460051/
https://www.ncbi.nlm.nih.gov/pubmed/26053048
http://dx.doi.org/10.1371/journal.pone.0129294
_version_ 1782375312352346112
author Yang, Wenxia
Zhang, Yuhong
Zhou, Xiaojin
Zhang, Wei
Xu, Xiaolu
Chen, Rumei
Meng, Qingchang
Yuan, Jianhua
Yang, Peilong
Yao, Bin
author_facet Yang, Wenxia
Zhang, Yuhong
Zhou, Xiaojin
Zhang, Wei
Xu, Xiaolu
Chen, Rumei
Meng, Qingchang
Yuan, Jianhua
Yang, Peilong
Yao, Bin
author_sort Yang, Wenxia
collection PubMed
description Raffinose-family oligosaccharide (RFO) in soybeans is one of the major anti-nutritional factors for poultry and livestocks. α-Galactosidase is commonly supplemented into the animal feed to hydrolyze α-1,6-galactosidic bonds on the RFOs. To simplify the feed processing, a protease-resistant α-galactosidase encoding gene from Gibberella sp. strain F75, aga-F75, was modified by codon optimization and heterologously expressed in the embryos of transgentic maize driven by the embryo-specific promoter ZM-leg1A. The progenies were produced by backcrossing with the commercial inbred variety Zheng58. PCR, southern blot and western blot analysis confirmed the stable integration and tissue specific expression of the modified gene, aga-F75m, in seeds over four generations. The expression level of Aga-F75M reached up to 10,000 units per kilogram of maize seeds. In comparison with its counterpart produced in Pichia pastoris strain GS115, maize seed-derived Aga-F75M showed a lower temperature optimum (50°C) and lower stability over alkaline pH range, but better thermal stability at 60°C to 70°C and resistance to feed pelleting inactivation (80°C). This is the first report of producing α-galactosidase in transgenic plant. The study offers an effective and economic approach for direct utilization of α-galactosidase-producing maize without any purification or supplementation procedures in the feed processing.
format Online
Article
Text
id pubmed-4460051
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-44600512015-06-16 Production of a Highly Protease-Resistant Fungal α-Galactosidase in Transgenic Maize Seeds for Simplified Feed Processing Yang, Wenxia Zhang, Yuhong Zhou, Xiaojin Zhang, Wei Xu, Xiaolu Chen, Rumei Meng, Qingchang Yuan, Jianhua Yang, Peilong Yao, Bin PLoS One Research Article Raffinose-family oligosaccharide (RFO) in soybeans is one of the major anti-nutritional factors for poultry and livestocks. α-Galactosidase is commonly supplemented into the animal feed to hydrolyze α-1,6-galactosidic bonds on the RFOs. To simplify the feed processing, a protease-resistant α-galactosidase encoding gene from Gibberella sp. strain F75, aga-F75, was modified by codon optimization and heterologously expressed in the embryos of transgentic maize driven by the embryo-specific promoter ZM-leg1A. The progenies were produced by backcrossing with the commercial inbred variety Zheng58. PCR, southern blot and western blot analysis confirmed the stable integration and tissue specific expression of the modified gene, aga-F75m, in seeds over four generations. The expression level of Aga-F75M reached up to 10,000 units per kilogram of maize seeds. In comparison with its counterpart produced in Pichia pastoris strain GS115, maize seed-derived Aga-F75M showed a lower temperature optimum (50°C) and lower stability over alkaline pH range, but better thermal stability at 60°C to 70°C and resistance to feed pelleting inactivation (80°C). This is the first report of producing α-galactosidase in transgenic plant. The study offers an effective and economic approach for direct utilization of α-galactosidase-producing maize without any purification or supplementation procedures in the feed processing. Public Library of Science 2015-06-08 /pmc/articles/PMC4460051/ /pubmed/26053048 http://dx.doi.org/10.1371/journal.pone.0129294 Text en © 2015 Yang 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
Yang, Wenxia
Zhang, Yuhong
Zhou, Xiaojin
Zhang, Wei
Xu, Xiaolu
Chen, Rumei
Meng, Qingchang
Yuan, Jianhua
Yang, Peilong
Yao, Bin
Production of a Highly Protease-Resistant Fungal α-Galactosidase in Transgenic Maize Seeds for Simplified Feed Processing
title Production of a Highly Protease-Resistant Fungal α-Galactosidase in Transgenic Maize Seeds for Simplified Feed Processing
title_full Production of a Highly Protease-Resistant Fungal α-Galactosidase in Transgenic Maize Seeds for Simplified Feed Processing
title_fullStr Production of a Highly Protease-Resistant Fungal α-Galactosidase in Transgenic Maize Seeds for Simplified Feed Processing
title_full_unstemmed Production of a Highly Protease-Resistant Fungal α-Galactosidase in Transgenic Maize Seeds for Simplified Feed Processing
title_short Production of a Highly Protease-Resistant Fungal α-Galactosidase in Transgenic Maize Seeds for Simplified Feed Processing
title_sort production of a highly protease-resistant fungal α-galactosidase in transgenic maize seeds for simplified feed processing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460051/
https://www.ncbi.nlm.nih.gov/pubmed/26053048
http://dx.doi.org/10.1371/journal.pone.0129294
work_keys_str_mv AT yangwenxia productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT zhangyuhong productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT zhouxiaojin productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT zhangwei productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT xuxiaolu productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT chenrumei productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT mengqingchang productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT yuanjianhua productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT yangpeilong productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing
AT yaobin productionofahighlyproteaseresistantfungalagalactosidaseintransgenicmaizeseedsforsimplifiedfeedprocessing