Molecular genetic studies of the cytochrome o terminal oxidase complex in Escherichia coli
Chepuri, Visala
This item is only available for download by members of the University of Illinois community. Students, faculty, and staff at the U of I may log in with your NetID and password to view the item. If you are trying to access an Illinois-restricted dissertation or thesis, you can request a copy through your library's Inter-Library Loan office or purchase a copy directly from ProQuest.
Permalink
https://hdl.handle.net/2142/21143
Description
Title
Molecular genetic studies of the cytochrome o terminal oxidase complex in Escherichia coli
Author(s)
Chepuri, Visala
Issue Date
1990
Doctoral Committee Chair(s)
Gennis, Robert B.
Department of Study
Biochemistry
Discipline
Biochemistry
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Biology, Molecular
Biology, Genetics
Chemistry, Biochemistry
Language
eng
Abstract
The cytochrome $o$ terminal oxidase complex is a component of aerobic respiratory chain of Escherichia coli. This enzyme catalyzes the oxidation of ubiquinol-8 to ubiquinone-8 within the cytoplasmic membrane and the concomitant reduction of O$\sb2$ to H$\sb2$O. Cytochrome $o$ oxidase has been purified and shown to contain four subunits on SDS-PAGE gels. The cloning of the $cyo$ operon makes it possible to address a number of problems concerning the structure and function of the cytochrome $o$ oxidase complex. Detailed analysis of this operon will enable us to identify the subunit compositions, the locations of the hemes, etc.
The thesis research described here has mainly dealt with the structure-function relationship of the cytochrome $o$ oxidase complex. Molecular biological, genetic and some biochemical approaches were used to study the following aspects of cytochrome $o$ oxidase complex: (i) sequence of the $cyo$ operon to determine the primary structure and subunit composition of the cytochrome $o$ oxidase complex, (ii) sequence portions of the polypeptides of cytochrome $o$ complex to correlate with the corresponding ORF's in the $cyo$ operon and to confirm the accuracy of the ORF's deduced by DNA sequence analysis, (iii) use the method of gene fusions to determine the topology of all the subunits of the cytochrome $o$ oxidase complex, (iv) construct a cyo-lacZ fusion and transfer it to the chromosome in order to study regulation in single copy, in this case by the $arc$ system, (v) localize both the cytochromes of the cytochrome $o$ oxidase complex by deletion analysis, and (vi) establish conditions in order to isolate HQNO resistant mutants of the cytochrome $o$ oxidase complex.
Use this login method if you
don't
have an
@illinois.edu
email address.
(Oops, I do have one)
IDEALS migrated to a new platform on June 23, 2022. If you created
your account prior to this date, you will have to reset your password
using the forgot-password link below.