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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
21

Methylmalonyl CoA mutase from Saccharopolyspora erythraea

McKie, Norman January 1992 (has links)
No description available.
22

Molecular studies of Theiler's murine encephalomyletis virus

Law, Katherine Mary January 1990 (has links)
No description available.
23

Wingless : A gene required for segmentation in Drosophila

Baker, N. E. January 1985 (has links)
No description available.
24

PCR generated gene probes for cloning fungal polykeptide synthase genes associated with squalestatin biosynthesis

Glod, Frank January 2003 (has links)
No description available.
25

The investigation of a membrane associated inositol 1,4,5-trisphosphate 3-kinase

Thomas, Stephen Gregory January 1996 (has links)
No description available.
26

CLONING OF BACTERIOPHAGE-PHI29 GENE 15; ISOLATION, OVERPRODUCTION AND PURIFICATION OF PHI29 LYTIC ENZYME.

SAEDI, MOHAMMAD SAEED. January 1987 (has links)
A spontaneous deletion mutant of Bacillus phage φ29 (φ29Δ1) is characterized in the first part of this study. This mutant has a 1,112 base pair deletion, which covers the entire coding sequence of genes 14 and 15 including the early promoter, B2. While lysis is very delayed, the phage DNA synthesis and internal phage development appears to be normal in the cells infected with this deletion mutant. These results indicate that the early functions are intact in φ29Δ1. Results also suggest that genes 14 and 15 are dispensable for bacteriophage φ29 growth, and that the B2 promoter may also be despensable for the early functions of φ29. To further explore the function of gene 15, a DNA fragment of φ29 chromosome, encoding the entire sequence of this gene, has been cloned into the Escherichia coli expression vector pPLc245, under the control of the phage lambda major early leftward promoter, PL. Upon heat induction, a protein with an apparent size of 26 kdal was over-produced. This protein has been purified to near homogeneity and confirmed to be the product of gene 15 by amino acid sequence analysis of its N terminus. The purified product of gene 15 has a lysozyme activity similar to the other phage-type lysozymes: products of phage T4 gene e and of phage P22 gene 19. This is the first lysozyme to be cloned and purified from a gram positive system. Bacteriophage φ29 lysozyme has been characterized in the last part of this study. Results show that this enzyme seems to more active than hen egg-white lysozyme against B. subtilis, E. coli, and M. lysodeikticus cells. Most of the characteristics of φ29 lysozyme appears to be similar to the P22 and T4 lysozymes, however, φ29 lysozyme seems to be about 2 times more thermostable than the other two lysozymes.
27

Studies on molecular cloning of the genes for the enzymes #alpha#-L-iduronidase and arylsulphatase A

Stephenson, J. January 1988 (has links)
No description available.
28

Bovine IgG Fc receptors

Zhang, Gaiping January 1994 (has links)
No description available.
29

The use of repetitive DNA sequences, in particular retrotransposons, in the genetic analysis of oil palm (Elaeis guineensis)

Moore, Catherine Samantha January 2000 (has links)
No description available.
30

The molecular basis of osteoblast adhesion

Townsend, Paul Andrew January 1997 (has links)
No description available.

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