Spelling suggestions: "subject:"haloacid dehalogenation"" "subject:"haloacids dehalogenation""
1 |
Heterologous expression and localization of cryptic haloacid dehalogenase Chd1 of Burkholderia cepacia MBA4 /Sze, Johnny. January 2001 (has links)
Thesis (M. Phil.)--University of Hong Kong, 2002. / Includes bibliographical references (leaves 145-174).
|
2 |
Heterologous expression and localization of cryptic haloacid dehalogenase Chd1 of Burkholderia cepacia MBA4施國雄, Sze, Johnny. January 2001 (has links)
published_or_final_version / Botany / Master / Master of Philosophy
|
3 |
Heterologous expression and immobilization of a haloalkane dehalogenase from Rhodococcus erythropolis Y2 /Wong, Pui-shan, Helen. January 2001 (has links)
Thesis (M. Phil.)--University of Hong Kong, 2002. / Includes bibliographical references (leaves 119-135).
|
4 |
Identification of the regulatory element of dehalogenase IVa of Burkholderia cepacia MBA4Chung, Yiu-kay, Wilson., 鍾堯基. January 2003 (has links)
published_or_final_version / abstract / toc / Botany / Master / Master of Philosophy
|
5 |
A study of the catabolite repression of the dehalogenase IVa gene of Burkholderia cepacia MBA4Yuen, Hiu-fung., 阮曉峰. January 2004 (has links)
published_or_final_version / abstract / toc / Botany / Master / Master of Philosophy
|
6 |
Heterologous expression and immobilization of a haloalkane dehalogenase from Rhodococcus erythropolis Y2黃佩珊, Wong, Pui-shan, Helen. January 2001 (has links)
published_or_final_version / Botany / Master / Master of Philosophy
|
7 |
A study of the catabolite repression of the dehalogenase IVa gene of Burkholderia cepacia MBA4Yuen, Hiu-fung. January 2004 (has links)
Thesis (M. Phil.)--University of Hong Kong, 2005. / Title proper from title frame. Also available in printed format.
|
8 |
Characterization of the promoter of dehalogenase IVa gene of Burkholderia sp. MBA4Chu, Ying-ying, Jamie., 朱盈盈. January 2006 (has links)
published_or_final_version / abstract / Botany / Master / Master of Philosophy
|
9 |
Characterization of the promoter of dehalogenase IVa gene of Burkholderia sp. MBA4Chu, Ying-ying, Jamie. January 2006 (has links)
Thesis (M. Phil.)--University of Hong Kong, 2007. / Title proper from title frame. Also available in printed format.
|
10 |
Activity-based Functional Annotation of Unknown Proteins: HAD-like hydrolases from E. coli and S. cerevisiaeKuznetsova, Ekaterina 18 February 2010 (has links)
In all sequenced genomes, a large fraction of predicted genes encodes proteins of unknown biochemical function and up to 15% of the genes with ‘‘known’’ function are mis-annotated. Several global approaches are being employed to predict function, including sequence similarity searches, analysis of gene expression, protein interaction, and protein structure. Enzymes comprise a group of target proteins that require experimental characterization for accurate functional annotations. Here I applied enzyme genomics to identify new enzymes by screening individually purified proteins for enzymatic activity under relaxed reaction conditions, which allowed me to identify the subclass or sub-subclasses of enzymes to which the unknown protein belongs. Further biochemical characterization of proteins was facilitated by the application of secondary screens with natural substrates (substrate profiling). Application of general enzymatic screens and substrate profiling greatly sped up the identification of biochemical function of unknown proteins and the experimental verification of functional predictions produced by other functional genomics approaches.
As a test case, I used this approach to characterize the members of the haloacid dehalogenase (HAD)-like hydrolase superfamily, which consists mainly of uncharacterized enzymes, with a few members shown to possess phosphatase, beta-phosphoglucomutase, phosphonatase, and dehalogenase activities. Low sequence similarity between the members of the HAD superfamily precludes the computational prediction of their substrates and functions. Using a representative set of 80 phosphorylated substrates I characterized the phosphatase activities of 21 soluble HADs from Escherichia coli and seven soluble HADs from Saccharomyces cerevisiae. E. coli HADs show broad and overlapping substrate specificity against a wide range of phosphorylated metabolites. The yeast enzymes were more specific, and one protein also showed protein phosphatase activity. Comparison of HAD substrate profiles from two model organisms showed several “functional niches” that are occupied by HADs, which include hydrolysis of nucleotides, phosphoglycolate, phosphoserine, and pyridoxal phosphate. I proposed the cellular function for a number of HADs from both organisms based on substrate specificities. The physiological relevance of the phosphatase activity with the preferred substrate was validated in vivo for one of the HADs, E. coli YniC.
|
Page generated in 0.0659 seconds