Cargando…

An Easy and Efficient Strategy for the Enhancement of Epothilone Production Mediated by TALE-TF and CRISPR/dcas9 Systems in Sorangium cellulosum

Epothilones are a kind of macrolides with strong cytotoxicity toward cancer cells and relatively lower side effects compared with taxol. Epothilone B derivate ixabepilone has been used for the clinical treatment of advanced breast cancer. However, the low yield of epothilones and the difficulty in t...

Descripción completa

Detalles Bibliográficos
Autores principales: Ye, Wei, Liu, Taomei, Zhu, Muzi, Zhang, Weimin, Huang, Zilei, Li, Saini, Li, Haohua, Kong, Yali, Chen, Yuchan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988809/
https://www.ncbi.nlm.nih.gov/pubmed/32039165
http://dx.doi.org/10.3389/fbioe.2019.00334
_version_ 1783492318907596800
author Ye, Wei
Liu, Taomei
Zhu, Muzi
Zhang, Weimin
Huang, Zilei
Li, Saini
Li, Haohua
Kong, Yali
Chen, Yuchan
author_facet Ye, Wei
Liu, Taomei
Zhu, Muzi
Zhang, Weimin
Huang, Zilei
Li, Saini
Li, Haohua
Kong, Yali
Chen, Yuchan
author_sort Ye, Wei
collection PubMed
description Epothilones are a kind of macrolides with strong cytotoxicity toward cancer cells and relatively lower side effects compared with taxol. Epothilone B derivate ixabepilone has been used for the clinical treatment of advanced breast cancer. However, the low yield of epothilones and the difficulty in the genetic manipulation of Sorangium cellulosum limited their wider application. Transcription activator-like effectors-Trancriptional factor (TALE-TF)-VP64 and clustered regularly interspaced short palindromic repeats (CRISPR)/dCas9-VP64 have been demonstrated as effective systems for the transcriptional improvement. In this study, a promoter for the epothilone biosynthesis cluster was obtained and the function has been verified. The TALE-TF-VP64 and CRISPR/dcas9-VP64 target P3 promoter were electroporated into S. cellulosum strain So ce M4, and the transcriptional levels of epothilone biosynthesis-related genes were significantly upregulated. The yield of epothilone B was improved by 2.89- and 1.53-fold by the introduction of recombinant TALE-TF-VP64-P3 and dCas9-VP64-P3 elements into So ce M4, respectively. The epothilone D yield was also improved by 1.12- and 2.18-fold in recombinant dCas9-So ce M4 and TALE-VP64 strains, respectively. The transcriptional regulation mechanism of TALE-TF-VP64 and the competition mechanism with endogenous transcriptional factor were investigated by electrophoretic mobility shift assay (EMSA) and chromatin immunoprecipitation (ChIP), demonstrating the combination of the P3 promoter and TALE-TF element and the competition between TALE-TF and endogenous transcriptional protein. This is the first report on the transcriptional regulation of the epothilone biosynthetic gene cluster in S. cellulosum using the TALE-TF and dCas9-VP64 systems, and the regulatory mechanism of the TALE-TF system for epothilone biosynthesis in S. cellulosum was also firstly revealed, thus shedding light on the metabolic engineering of S. cellulosum to improve epothilone yields substantially and promoting the application of epothilones in the biomedical industry.
format Online
Article
Text
id pubmed-6988809
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-69888092020-02-07 An Easy and Efficient Strategy for the Enhancement of Epothilone Production Mediated by TALE-TF and CRISPR/dcas9 Systems in Sorangium cellulosum Ye, Wei Liu, Taomei Zhu, Muzi Zhang, Weimin Huang, Zilei Li, Saini Li, Haohua Kong, Yali Chen, Yuchan Front Bioeng Biotechnol Bioengineering and Biotechnology Epothilones are a kind of macrolides with strong cytotoxicity toward cancer cells and relatively lower side effects compared with taxol. Epothilone B derivate ixabepilone has been used for the clinical treatment of advanced breast cancer. However, the low yield of epothilones and the difficulty in the genetic manipulation of Sorangium cellulosum limited their wider application. Transcription activator-like effectors-Trancriptional factor (TALE-TF)-VP64 and clustered regularly interspaced short palindromic repeats (CRISPR)/dCas9-VP64 have been demonstrated as effective systems for the transcriptional improvement. In this study, a promoter for the epothilone biosynthesis cluster was obtained and the function has been verified. The TALE-TF-VP64 and CRISPR/dcas9-VP64 target P3 promoter were electroporated into S. cellulosum strain So ce M4, and the transcriptional levels of epothilone biosynthesis-related genes were significantly upregulated. The yield of epothilone B was improved by 2.89- and 1.53-fold by the introduction of recombinant TALE-TF-VP64-P3 and dCas9-VP64-P3 elements into So ce M4, respectively. The epothilone D yield was also improved by 1.12- and 2.18-fold in recombinant dCas9-So ce M4 and TALE-VP64 strains, respectively. The transcriptional regulation mechanism of TALE-TF-VP64 and the competition mechanism with endogenous transcriptional factor were investigated by electrophoretic mobility shift assay (EMSA) and chromatin immunoprecipitation (ChIP), demonstrating the combination of the P3 promoter and TALE-TF element and the competition between TALE-TF and endogenous transcriptional protein. This is the first report on the transcriptional regulation of the epothilone biosynthetic gene cluster in S. cellulosum using the TALE-TF and dCas9-VP64 systems, and the regulatory mechanism of the TALE-TF system for epothilone biosynthesis in S. cellulosum was also firstly revealed, thus shedding light on the metabolic engineering of S. cellulosum to improve epothilone yields substantially and promoting the application of epothilones in the biomedical industry. Frontiers Media S.A. 2019-11-26 /pmc/articles/PMC6988809/ /pubmed/32039165 http://dx.doi.org/10.3389/fbioe.2019.00334 Text en Copyright © 2019 Ye, Liu, Zhu, Zhang, Huang, Li, Li, Kong and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Ye, Wei
Liu, Taomei
Zhu, Muzi
Zhang, Weimin
Huang, Zilei
Li, Saini
Li, Haohua
Kong, Yali
Chen, Yuchan
An Easy and Efficient Strategy for the Enhancement of Epothilone Production Mediated by TALE-TF and CRISPR/dcas9 Systems in Sorangium cellulosum
title An Easy and Efficient Strategy for the Enhancement of Epothilone Production Mediated by TALE-TF and CRISPR/dcas9 Systems in Sorangium cellulosum
title_full An Easy and Efficient Strategy for the Enhancement of Epothilone Production Mediated by TALE-TF and CRISPR/dcas9 Systems in Sorangium cellulosum
title_fullStr An Easy and Efficient Strategy for the Enhancement of Epothilone Production Mediated by TALE-TF and CRISPR/dcas9 Systems in Sorangium cellulosum
title_full_unstemmed An Easy and Efficient Strategy for the Enhancement of Epothilone Production Mediated by TALE-TF and CRISPR/dcas9 Systems in Sorangium cellulosum
title_short An Easy and Efficient Strategy for the Enhancement of Epothilone Production Mediated by TALE-TF and CRISPR/dcas9 Systems in Sorangium cellulosum
title_sort easy and efficient strategy for the enhancement of epothilone production mediated by tale-tf and crispr/dcas9 systems in sorangium cellulosum
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988809/
https://www.ncbi.nlm.nih.gov/pubmed/32039165
http://dx.doi.org/10.3389/fbioe.2019.00334
work_keys_str_mv AT yewei aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT liutaomei aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT zhumuzi aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT zhangweimin aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT huangzilei aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT lisaini aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT lihaohua aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT kongyali aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT chenyuchan aneasyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT yewei easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT liutaomei easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT zhumuzi easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT zhangweimin easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT huangzilei easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT lisaini easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT lihaohua easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT kongyali easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum
AT chenyuchan easyandefficientstrategyfortheenhancementofepothiloneproductionmediatedbytaletfandcrisprdcas9systemsinsorangiumcellulosum