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Inserts amplification for knockout cassette construction

Description

The goal of the study was to obtain optimal conditions for amplification of upstream and downstream genes fragments and introduce a cleavage site for restriction enzymes into them thanks to which it will be possible to clone fragments into a plasmid containing elements of the knockout cassette. The constructed cassettes will enable the removal of the tested genes from the C. albicans SC5314 genome using the SAT1-flipper method.

The deletion of tested genes encoding enzymes O-acetylhomoserine sulfhydrylases Met15p, homoserine O-acetyltransferases Met2p and cystathionine-γ-synthases Str2p enable the assessment of the impact of those enzymes on the phenotype of cells, on the virulence of the strain, and allows to recognize the in vivo function of the tested proteins in L-methionine biosynthesis.

The studies were financially supported from the project OPUS 20 financed by the National Science Centre (No. UMO-2020/39/B/NZ7/01519).

Dataset file

Inserts amplification for knockout cassette construction.zip
778.9 kB, S3 ETag 289772929df6d9dbe2510418cfb8a2ce-1, downloads: 65
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download file Inserts amplification for knockout cassette construction.zip

File details

License:
Creative Commons: by 4.0 open in new tab
CC BY
Attribution
Raw data:
Data contained in dataset was not processed.

Details

Year of publication:
2023
Verification date:
2023-03-30
Dataset language:
English
Fields of science:
  • chemical sciences (Natural sciences)
DOI:
DOI ID 10.34808/xak8-rr65 open in new tab
Funding:
Verified by:
Gdańsk University of Technology

Keywords

References

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