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Thèses Canada
Item – Thèses Canada
Contenu de la page
Item – Thèses Canada
Numéro d'OCLC
1032905850
Lien(s) vers le texte intégral
Exemplaire de BAC
Exemplaire de BAC
Auteur
Ding, Jie Ping.
Titre
In vivo studies of CRP and LRP in the regulation of sdaA, serA and metK genes in Escherichia coli K-12.
Diplôme
Theses (M. Sc.) -- Concordia University, 2002
Éditeur
Montréal : Concordia University, 2002.
Description
1 online resource
Notes
Includes bibliographical references.
Résumé
The sdaA gene of Escherichia coli encodes L-serine deaminase (L-SD), which degrades L-serine to ammonia and pyruvate. LRP represses the expression of both L-SD and sdaA . CRP was assumed to affect sdaA transcription, but this had not been proven. I demonstrated here that both CRP and LRP were involved in L-SD and sdaA expression. LRP repressed L-SD expression and sdaA transcription. CRP activated L-SD expression depending on the presence of LRP but did not affect sdaA transcription. The genes for serA and metK are known to be regulated by LRP and are proposed to be regulated by CRP. CRP activated the serA P2 promoter. However, it did not affect serA expression overall. CRP was also involved in the regulation of metK expression through an unclear mechanism. By providing ptsG expression on a plasmid, I identified one factor causing the slow growth rate of crp mutants. The rate of glucose uptake was suggested to affect the growth rate of crp mutants.
Autre lien(s)
spectrum.library.concordia.ca
spectrum.library.concordia.ca
Date de modification :
2022-09-01