DocumentCode
3148754
Title
Disruption of PDC1 Gene to Enhance Pyruvic Acid Accumulation of Saccharomyces cerevisiae
Author
Wang De-pei ; Ding Xin ; Deng Xu-heng ; Zhao Qin ; Gao Qiang ; Gao Nian-fa
Author_Institution
Sch. of Biotechnol., Tianjin Univ. of Sci. & Technol., Tianjin, China
fYear
2010
fDate
18-20 June 2010
Firstpage
1
Lastpage
3
Abstract
The PDC1 gene encoding a pyruvate decarboxylase in S. cerevisiae and Kanr gene were respectively amplified by PCR using oligonucleotides which contained the restriction of NotI, EcoRI, and BglII. The two genes were digested with the same EcoRI and BglII, and linked together for inserting the Kanr gene into the PDC1 gene while the gene disruption cassette was constructed. After transformation of the linear disruption cassette (P1K) into S. cerevisiae Y2, selected transformants were checked by PCR for correct recombination. The haploid mutant Y2-1Δ was obtained, which could increase the yield of pyruvic acid by 176% by shaking flask cultivation as compared with the parental strain Y2.
Keywords
biochemistry; cellular biophysics; fermentation; genetic engineering; genetics; genomics; microorganisms; molecular biophysics; Kanr gene; PCR; PDC1gene encoding; S. cerevisiae; Saccharomyces cerevisiae; gene disruption cassette; linear disruption cassette; oligonucleotides; pyruvate decarboxylase; pyruvic acid; shake flask fermentation; shaking flask cultivation; Biochemistry; Bioinformatics; Biotechnology; Capacitive sensors; DNA; Ethanol; Genomics; Immune system; Laboratories; Sugar;
fLanguage
English
Publisher
ieee
Conference_Titel
Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
Conference_Location
Chengdu
ISSN
2151-7614
Print_ISBN
978-1-4244-4712-1
Electronic_ISBN
2151-7614
Type
conf
DOI
10.1109/ICBBE.2010.5517871
Filename
5517871
Link To Document