Your browser does not allow JavaScript!
JavaScript is necessary for the proper functioning of this website. Please enable JavaScript or use a modern browser.
Open Science Slovenia
Open Science
DiKUL
slv
|
eng
Search
Browse
New in RUL
About RUL
In numbers
Help
Sign in
Simple and reliable in situ CRISPR-Cas9 nuclease visualization tool is ensuring efficient editing in Streptomyces species
ID
Pšeničnik, Alen
(
Author
),
ID
Reberšek, Roman
(
Author
),
ID
Slemc, Lucija
(
Author
),
ID
Godec, Tim
(
Author
),
ID
Kranjc, Luka
(
Author
),
ID
Petković, Hrvoje
(
Author
)
PDF - Presentation file,
Download
(3,24 MB)
MD5: 96931501F3A6A75FE7D0637796D77B3C
URL - Source URL, Visit
https://www.sciencedirect.com/science/article/pii/S0167701222001403
Image galllery
Abstract
CRISPR-Cas9 technology has emerged as a promising tool for genetic engineering of Streptomyces strains. However, in practice, numerous technical hurdles have yet to be overcome when developing robust editing procedures. Here, we developed an extension of the CRISPR-Cas toolbox, a simple and reliable cas9 monitoring tool with transcriptional fusion of cas9 nuclease to a beta glucuronidase (gusA) visual reporter gene. The Cas9-SD-GusA tool enables in situ identification of cells expressing Cas9 nuclease following the introduction of the plasmid carrying the CRISPR-Cas9 machinery. Remarkably, when the Cas9-SD-GusA system was applied under optimal conditions, 100% of the colonies displaying GusA activity carried the target genotype. In contrast, it was shown that the cas9 sequence had undergone major recombination events in the colonies that did not exhibit GusA activity, giving rise to “escaper colonies” carrying unedited genotype. Our approach allows a simple detection of “escaper” phenotype and serves as an efficient CRISPR-Cas9 optimisation tool.
Language:
English
Keywords:
CRISPR-Cas9
,
gusA visual screening
,
CRISPR escaper colonies
,
Streptomyces
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
BF - Biotechnical Faculty
Publication status:
Published
Publication version:
Version of Record
Year:
2022
Number of pages:
7 str.
Numbering:
Vol. 200, art. 106545
PID:
20.500.12556/RUL-141957
UDC:
602.6:579.873.7
ISSN on article:
0167-7012
DOI:
10.1016/j.mimet.2022.106545
COBISS.SI-ID:
122035715
Publication date in RUL:
12.10.2022
Views:
725
Downloads:
132
Metadata:
Cite this work
Plain text
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Copy citation
Share:
Record is a part of a journal
Title:
Journal of microbiological methods
Shortened title:
J. microbiol. methods
Publisher:
Elsevier
ISSN:
0167-7012
COBISS.SI-ID:
25764864
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Secondary language
Language:
Slovenian
Keywords:
genski inženiring
,
genska modifikacija
,
CRISPR
,
Cas9
,
aktinomicete
,
Streptomyces rimosus
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
P4-0116
Name:
Mikrobiologija in biotehnologija živil in okolja
Funder:
ARRS - Slovenian Research Agency
Funding programme:
Young researchers
Similar documents
Similar works from RUL:
Similar works from other Slovenian collections:
Back