Cloning and expression of recombinant xylanase enzyme (xynA) in E. coli.

Objective Today, global increasing in corn prices has led to the replacement of wheat instead of corn in poultry diets. The NSPs in the cell wall prevents the uptake of wheat nutrients by poultry. Using xylanase is one of the methods to remove NSPs. Xylanases can digest xylan. The aim of current inv...

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Main Authors: Amin Sadeghi Alikelayeh, Neda Mirakhorli, Mohammad Reza Akbari, Behzad Shareghi Brojeni
Format: Article
Language:fas
Published: Shahid Bahonar University of Kerman 2021-01-01
Series:مجله بیوتکنولوژی کشاورزی
Subjects:
Online Access:https://jab.uk.ac.ir/article_2774_989bbdd1904e85e3aae1007ca01218e8.pdf
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author Amin Sadeghi Alikelayeh
Neda Mirakhorli
Mohammad Reza Akbari
Behzad Shareghi Brojeni
author_facet Amin Sadeghi Alikelayeh
Neda Mirakhorli
Mohammad Reza Akbari
Behzad Shareghi Brojeni
author_sort Amin Sadeghi Alikelayeh
collection DOAJ
description Objective Today, global increasing in corn prices has led to the replacement of wheat instead of corn in poultry diets. The NSPs in the cell wall prevents the uptake of wheat nutrients by poultry. Using xylanase is one of the methods to remove NSPs. Xylanases can digest xylan. The aim of current investigation was to produce xylanase (xynA) gene as a supplement of poultry diets in E. coli. Materials and methods In present study, the thermostable xylanase (xynA) gene in a bacterial secretory expression system along with: Shine-Dalgarno sequence, Usp45 signal peptide and T7 promoter was cloned in plasmid pET-22b (+) from E. coli strain BL21 (DE3) using The heat shock method. IPTG were used at different times to induce the expression of recombinant xylanase gene. In addition, catalytic indicators were done according to the DNS method.   Results PCR colony confirmed the presence of 743 bp recombinant xylanase gene sequence on 1% agarose gel. SDS-PAGE showed protein with 27 kDa molecular weight. Also, the activity of recombinant protein was 189.47 (unit/ml) using DNS method at optimum temperature of 65 °C and pH=6. As well as, michaelis-menten curve determined Km and Vmax 4.1 (mg/ml) and 87 (unit/ml), respectively.   Conclusions Xylanase are the most important complementary enzymes in poultry diets that are added to wheat-based diets. Results showed that produced recombinant xylanase is thermostable enzyme with acceptable activity and concentration. Furthermore, because of the secretory expression system, it is produced at a lower cost.
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spelling doaj.art-2f37a7a64a7f409283113c90dfb52db12023-12-16T17:40:46ZfasShahid Bahonar University of Kermanمجله بیوتکنولوژی کشاورزی2228-67052228-65002021-01-0112412110.22103/jab.2020.16372.12552774Cloning and expression of recombinant xylanase enzyme (xynA) in E. coli.Amin Sadeghi Alikelayeh0Neda Mirakhorli1Mohammad Reza Akbari2Behzad Shareghi Brojeni3Department of Biotechnology, Faculty of Agriculture, University of Shahrekord, Chaharmahal and baktyari province, IRANAssistant Professor, Department of Biotechnology and Plant Breeding, Faculty of Agriculture, Shahrekord University, Shahrekord, IranAssistant Professor, Department of Animal and Poultry Science, Faculty of Agriculture, Shahrekord University, Shahrekord, IranProfessor, Department of Biochemistry, Faculty of Basic Science, Shahrekord University, Shahrekord, Iran.Objective Today, global increasing in corn prices has led to the replacement of wheat instead of corn in poultry diets. The NSPs in the cell wall prevents the uptake of wheat nutrients by poultry. Using xylanase is one of the methods to remove NSPs. Xylanases can digest xylan. The aim of current investigation was to produce xylanase (xynA) gene as a supplement of poultry diets in E. coli. Materials and methods In present study, the thermostable xylanase (xynA) gene in a bacterial secretory expression system along with: Shine-Dalgarno sequence, Usp45 signal peptide and T7 promoter was cloned in plasmid pET-22b (+) from E. coli strain BL21 (DE3) using The heat shock method. IPTG were used at different times to induce the expression of recombinant xylanase gene. In addition, catalytic indicators were done according to the DNS method.   Results PCR colony confirmed the presence of 743 bp recombinant xylanase gene sequence on 1% agarose gel. SDS-PAGE showed protein with 27 kDa molecular weight. Also, the activity of recombinant protein was 189.47 (unit/ml) using DNS method at optimum temperature of 65 °C and pH=6. As well as, michaelis-menten curve determined Km and Vmax 4.1 (mg/ml) and 87 (unit/ml), respectively.   Conclusions Xylanase are the most important complementary enzymes in poultry diets that are added to wheat-based diets. Results showed that produced recombinant xylanase is thermostable enzyme with acceptable activity and concentration. Furthermore, because of the secretory expression system, it is produced at a lower cost.https://jab.uk.ac.ir/article_2774_989bbdd1904e85e3aae1007ca01218e8.pdfrecombinant xylanase enzymee. coliwheat
spellingShingle Amin Sadeghi Alikelayeh
Neda Mirakhorli
Mohammad Reza Akbari
Behzad Shareghi Brojeni
Cloning and expression of recombinant xylanase enzyme (xynA) in E. coli.
مجله بیوتکنولوژی کشاورزی
recombinant xylanase enzyme
e. coli
wheat
title Cloning and expression of recombinant xylanase enzyme (xynA) in E. coli.
title_full Cloning and expression of recombinant xylanase enzyme (xynA) in E. coli.
title_fullStr Cloning and expression of recombinant xylanase enzyme (xynA) in E. coli.
title_full_unstemmed Cloning and expression of recombinant xylanase enzyme (xynA) in E. coli.
title_short Cloning and expression of recombinant xylanase enzyme (xynA) in E. coli.
title_sort cloning and expression of recombinant xylanase enzyme xyna in e coli
topic recombinant xylanase enzyme
e. coli
wheat
url https://jab.uk.ac.ir/article_2774_989bbdd1904e85e3aae1007ca01218e8.pdf
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AT nedamirakhorli cloningandexpressionofrecombinantxylanaseenzymexynainecoli
AT mohammadrezaakbari cloningandexpressionofrecombinantxylanaseenzymexynainecoli
AT behzadshareghibrojeni cloningandexpressionofrecombinantxylanaseenzymexynainecoli