Cargando…

Functional expression of recombinant human trefoil factor 1 by Escherichia coli and Brevibacillus choshinensis

BACKGROUND: Trefoil factor 1 (TFF1) mediates mucosal repair and belongs to a highly conserved trefoil factor family proteins which are secreted by epithelial cells in the stomach or colon mucous membrane. TFF1 forms a homodimer via a disulphide linkage that affects wound healing activity. Previous r...

Descripción completa

Detalles Bibliográficos
Autores principales: Cheng, Yueh-Mei, Lu, Meng-Ting, Yeh, Chuan Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438461/
https://www.ncbi.nlm.nih.gov/pubmed/25990322
http://dx.doi.org/10.1186/s12896-015-0149-5
_version_ 1782372337732026368
author Cheng, Yueh-Mei
Lu, Meng-Ting
Yeh, Chuan Mei
author_facet Cheng, Yueh-Mei
Lu, Meng-Ting
Yeh, Chuan Mei
author_sort Cheng, Yueh-Mei
collection PubMed
description BACKGROUND: Trefoil factor 1 (TFF1) mediates mucosal repair and belongs to a highly conserved trefoil factor family proteins which are secreted by epithelial cells in the stomach or colon mucous membrane. TFF1 forms a homodimer via a disulphide linkage that affects wound healing activity. Previous recombinant expressions of TFF1 were too low yield for industrial application. This study aims to improve the expression level of bioactive recombinant TFF1 (rTFF1) and facilitate application potency. METHODS: The rTFF1 gene rtff1 was synthesized, expressed by Escherichia coli and secreted by Brevibacillus choshinensis. The rTFF1s were purified. The polymeric patterns and wound healing capacities of purified rTFF1s were checked. RESULTS: In Escherichia coli, 21.08 mg/L rTFF1 was stably expressed as monomer, dimer and oligomer in soluble fraction. In Brevebacillus choshinensis, the rTFF1 was secreted extracellularly at high level (35.73 mg/L) and formed monomer, dimer and oligomer forms. Both proteins from different sources were purified by Ni-NTA chromatography and exhibited the wound healing activities. The rTFF1 produced by B. choshinensis had better wound healing capability than the rTFF1 produced by E. coli. After pH 2.4 buffer treatments, the purified rTFF1 formed more oligomeric forms as well as better wound healing capability. Glycosylation assay and LC-MS/MS spectrometry experiments showed that the rTFF1 produced by B. choshinensis was unexpectedly glycosylated at N-terminal Ser residue. The glycosylation may contribute to the better wound healing capacity. CONCLUSIONS: This study provides a potent tool of rTFF1 production to be applied in gastric damage protection and wound healing. The protein sources from B. choshinensis were more efficient than rTFF1 produced by E. coli. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-015-0149-5) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4438461
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-44384612015-05-21 Functional expression of recombinant human trefoil factor 1 by Escherichia coli and Brevibacillus choshinensis Cheng, Yueh-Mei Lu, Meng-Ting Yeh, Chuan Mei BMC Biotechnol Research Article BACKGROUND: Trefoil factor 1 (TFF1) mediates mucosal repair and belongs to a highly conserved trefoil factor family proteins which are secreted by epithelial cells in the stomach or colon mucous membrane. TFF1 forms a homodimer via a disulphide linkage that affects wound healing activity. Previous recombinant expressions of TFF1 were too low yield for industrial application. This study aims to improve the expression level of bioactive recombinant TFF1 (rTFF1) and facilitate application potency. METHODS: The rTFF1 gene rtff1 was synthesized, expressed by Escherichia coli and secreted by Brevibacillus choshinensis. The rTFF1s were purified. The polymeric patterns and wound healing capacities of purified rTFF1s were checked. RESULTS: In Escherichia coli, 21.08 mg/L rTFF1 was stably expressed as monomer, dimer and oligomer in soluble fraction. In Brevebacillus choshinensis, the rTFF1 was secreted extracellularly at high level (35.73 mg/L) and formed monomer, dimer and oligomer forms. Both proteins from different sources were purified by Ni-NTA chromatography and exhibited the wound healing activities. The rTFF1 produced by B. choshinensis had better wound healing capability than the rTFF1 produced by E. coli. After pH 2.4 buffer treatments, the purified rTFF1 formed more oligomeric forms as well as better wound healing capability. Glycosylation assay and LC-MS/MS spectrometry experiments showed that the rTFF1 produced by B. choshinensis was unexpectedly glycosylated at N-terminal Ser residue. The glycosylation may contribute to the better wound healing capacity. CONCLUSIONS: This study provides a potent tool of rTFF1 production to be applied in gastric damage protection and wound healing. The protein sources from B. choshinensis were more efficient than rTFF1 produced by E. coli. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-015-0149-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-20 /pmc/articles/PMC4438461/ /pubmed/25990322 http://dx.doi.org/10.1186/s12896-015-0149-5 Text en © Cheng et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Cheng, Yueh-Mei
Lu, Meng-Ting
Yeh, Chuan Mei
Functional expression of recombinant human trefoil factor 1 by Escherichia coli and Brevibacillus choshinensis
title Functional expression of recombinant human trefoil factor 1 by Escherichia coli and Brevibacillus choshinensis
title_full Functional expression of recombinant human trefoil factor 1 by Escherichia coli and Brevibacillus choshinensis
title_fullStr Functional expression of recombinant human trefoil factor 1 by Escherichia coli and Brevibacillus choshinensis
title_full_unstemmed Functional expression of recombinant human trefoil factor 1 by Escherichia coli and Brevibacillus choshinensis
title_short Functional expression of recombinant human trefoil factor 1 by Escherichia coli and Brevibacillus choshinensis
title_sort functional expression of recombinant human trefoil factor 1 by escherichia coli and brevibacillus choshinensis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438461/
https://www.ncbi.nlm.nih.gov/pubmed/25990322
http://dx.doi.org/10.1186/s12896-015-0149-5
work_keys_str_mv AT chengyuehmei functionalexpressionofrecombinanthumantrefoilfactor1byescherichiacoliandbrevibacilluschoshinensis
AT lumengting functionalexpressionofrecombinanthumantrefoilfactor1byescherichiacoliandbrevibacilluschoshinensis
AT yehchuanmei functionalexpressionofrecombinanthumantrefoilfactor1byescherichiacoliandbrevibacilluschoshinensis