Cargando…

Cloning and Expression of Yak Active Chymosin in Pichia pastoris

Rennet, a complex of enzymes found in the stomachs of ruminants, is an important component for cheese production. In our study, we described that yak chymosin gene recombinant Pichia pastoris strain could serve as a novel source for rennet production. Yaks total RNA was extracted from the abomasum o...

Descripción completa

Detalles Bibliográficos
Autores principales: Luo, Fan, Jiang, Wei Hua, Yang, Yuan Xiao, Li, Jiang, Jiang, Ming Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003999/
https://www.ncbi.nlm.nih.gov/pubmed/27004812
http://dx.doi.org/10.5713/ajas.16.0038
_version_ 1782450722079506432
author Luo, Fan
Jiang, Wei Hua
Yang, Yuan Xiao
Li, Jiang
Jiang, Ming Feng
author_facet Luo, Fan
Jiang, Wei Hua
Yang, Yuan Xiao
Li, Jiang
Jiang, Ming Feng
author_sort Luo, Fan
collection PubMed
description Rennet, a complex of enzymes found in the stomachs of ruminants, is an important component for cheese production. In our study, we described that yak chymosin gene recombinant Pichia pastoris strain could serve as a novel source for rennet production. Yaks total RNA was extracted from the abomasum of an unweaned yak. The yak preprochymosin, prochymosin, and chymosin genes from total RNA were isolated using gene specific primers based on cattle chymosin gene sequence respectively and analyzed their expression pattern byreal time-polymerase chain reaction. The result showed that the chymosin gene expression level of the sucking yaks was 11.45 times higher than one of adult yaks and yak chymosin belongs to Bovidae family in phylogenetic analysis. To express each, the preprochymosin, prochymosin, and chymosin genes were ligated into the expression vector pPICZαA, respectively, and were expressed in Pichia pastoris X33. The results showed that all the recombinant clones of P. pastoris containing the preprochymosin, prochymosin or chymosin genes could produce the active form of recombinant chymosin into the culture supernatant. Heterologous expressed prochymosin (14.55 Soxhlet unit/mL) had the highest enzyme activity of the three expressed chymosin enzymes. Therefore, we suggest that the yak chymosin gene recombinant Pichia pastoris strain could provide an alternative source of rennet production.
format Online
Article
Text
id pubmed-5003999
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST)
record_format MEDLINE/PubMed
spelling pubmed-50039992016-09-01 Cloning and Expression of Yak Active Chymosin in Pichia pastoris Luo, Fan Jiang, Wei Hua Yang, Yuan Xiao Li, Jiang Jiang, Ming Feng Asian-Australas J Anim Sci Article Rennet, a complex of enzymes found in the stomachs of ruminants, is an important component for cheese production. In our study, we described that yak chymosin gene recombinant Pichia pastoris strain could serve as a novel source for rennet production. Yaks total RNA was extracted from the abomasum of an unweaned yak. The yak preprochymosin, prochymosin, and chymosin genes from total RNA were isolated using gene specific primers based on cattle chymosin gene sequence respectively and analyzed their expression pattern byreal time-polymerase chain reaction. The result showed that the chymosin gene expression level of the sucking yaks was 11.45 times higher than one of adult yaks and yak chymosin belongs to Bovidae family in phylogenetic analysis. To express each, the preprochymosin, prochymosin, and chymosin genes were ligated into the expression vector pPICZαA, respectively, and were expressed in Pichia pastoris X33. The results showed that all the recombinant clones of P. pastoris containing the preprochymosin, prochymosin or chymosin genes could produce the active form of recombinant chymosin into the culture supernatant. Heterologous expressed prochymosin (14.55 Soxhlet unit/mL) had the highest enzyme activity of the three expressed chymosin enzymes. Therefore, we suggest that the yak chymosin gene recombinant Pichia pastoris strain could provide an alternative source of rennet production. Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2016-09 2016-03-22 /pmc/articles/PMC5003999/ /pubmed/27004812 http://dx.doi.org/10.5713/ajas.16.0038 Text en Copyright © 2016 by Asian-Australasian Journal of Animal Sciences This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Luo, Fan
Jiang, Wei Hua
Yang, Yuan Xiao
Li, Jiang
Jiang, Ming Feng
Cloning and Expression of Yak Active Chymosin in Pichia pastoris
title Cloning and Expression of Yak Active Chymosin in Pichia pastoris
title_full Cloning and Expression of Yak Active Chymosin in Pichia pastoris
title_fullStr Cloning and Expression of Yak Active Chymosin in Pichia pastoris
title_full_unstemmed Cloning and Expression of Yak Active Chymosin in Pichia pastoris
title_short Cloning and Expression of Yak Active Chymosin in Pichia pastoris
title_sort cloning and expression of yak active chymosin in pichia pastoris
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003999/
https://www.ncbi.nlm.nih.gov/pubmed/27004812
http://dx.doi.org/10.5713/ajas.16.0038
work_keys_str_mv AT luofan cloningandexpressionofyakactivechymosininpichiapastoris
AT jiangweihua cloningandexpressionofyakactivechymosininpichiapastoris
AT yangyuanxiao cloningandexpressionofyakactivechymosininpichiapastoris
AT lijiang cloningandexpressionofyakactivechymosininpichiapastoris
AT jiangmingfeng cloningandexpressionofyakactivechymosininpichiapastoris