𝔖 Bobbio Scriptorium
✦   LIBER   ✦

In-vitro recombination in rad and rnc mutants ofSaccharomyces cerevisiae

✍ Scribed by Peter D. Moore; John R. Simon; Linda J. Wallace; Terry Y. -K. Chow


Publisher
Springer-Verlag
Year
1993
Tongue
English
Weight
829 KB
Volume
23
Category
Article
ISSN
0172-8083

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Transformation and recombination in rad
✍ Simon, John R. ;Moore, Peter D. πŸ“‚ Article πŸ“… 1990 πŸ› Springer 🌐 English βš– 908 KB

Disruption/deletion mutations in genes of the RAD52 epistasis group of Saccharomyces cerevisiae were examined for their effects on recombination between single- and double-stranded circular DNA substrates and chromosomal genes in a transformation assay. In rad50 mutants there was a small reduction i

Anaerobic and aerobic batch cultivations
✍ Nissen, Torben L.; Hamann, Claus W.; Kielland-Brandt, Morten C.; Nielsen, Jens; πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 145 KB

Glycerol is formed as a by-product in production of ethanol and baker's yeast during fermentation of Saccharomyces cerevisiae under anaerobic and aerobic growth conditions, respectively. One physiological role of glycerol formation by yeast is to reoxidize NADH, formed in synthesis of biomass and se

Defective thymine dimer excision in radi
✍ Prakash, Louise πŸ“‚ Article πŸ“… 1977 πŸ› Springer 🌐 English βš– 384 KB

Two rad mutants of yeast, rad10 and rad16, are shown to be defective in the removal of UV-induced pyrimidine dimers since DNAs obtained from irradiated cells following a post-irradiation incubation in the dark still retain UV-endonuclease-sensitive sites. Both rad10 and rad16 mutants are in the same

Construction and physiological character
✍ JΓΌrgen Heinisch πŸ“‚ Article πŸ“… 1986 πŸ› Springer-Verlag 🌐 English βš– 730 KB

The structural genes coding for the two kinds of subunits of phosphofructokinase in yeast have been cloned previously (Heinisch 1986). The coding regions were defined by S1-mapping. They were disrupted in vitro by insertion of a LEU2-marker. These constructions were then used for substitution of the