๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Phosphorylation in living yeast cells

โœ Scribed by Rothstein, Aser


Book ID
102877932
Publisher
Wiley (John Wiley & Sons)
Year
1946
Tongue
English
Weight
525 KB
Volume
28
Category
Article
ISSN
0095-9898

No coin nor oath required. For personal study only.

โœฆ Synopsis


In recent years, a great deal of evidence has accumulated indicating that carbohydrate metabolism involves phosphorylated intermediaries (see reviews of Lipmann, '41 ; Kalcker, '42; and Cori, '42). Most of this evidence has been adduced from the study of tissue extracts and relatively simple sys- tpms of enzymes and substrates. Phosphorylation in intact cells is more difficult to demonstrate because steady states may exist whereby phosphorylated compounds are decomposed almost as rapidly as they are synthesized, with little net change in concentration.

Changes in the concentrations of various phosphate fractions have been demonstrated in the living yeast cells, during anaerobic metabolism of sugar (Levitov, '36; Ostern et al., '38 ; Kruyk and Klingmuller, '39 ; I\lcFar.lane, '39 ; and bIirslci and Wertheimer, '39).

I n this paper further evidence will be presented concerning the relationship of phosphorylation to carbohydrate metabolism in the living yeast cell, with special reference to aerobic metabolism. METHODS Fresh Baker's yeast (Standard Brands Inc.) was used for all experiments. The yeast was washed twice and suspended in the experimental medium. During washing, the centrifugal Present Address : Biochemistry and Pharmacology Department, School of Mectirinr and Dentistry, T!niversit>7 of Rochester, Rochester, N. Y.


๐Ÿ“œ SIMILAR VOLUMES


Tracking phosphorylation in live cells
โœ DeWitt, Natalie ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Nature Publishing Group ๐ŸŒ English โš– 145 KB
Interfacing Living Yeast Cells with Grap
โœ Sung Ho Yang; Taemin Lee; Eunyong Seo; Eun Hyea Ko; Insung S. Choi; Byeong-Su Ki ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 506 KB

## Abstract The first example of the encapsulation of living yeast cells with multilayers of GO nanosheets via LbL selfโ€assembly is reported. The GO nanosheets with opposite charges are alternatively coated onto the individual yeast cells while preserving the viability of the yeast cells, thus affo

Quantitative imaging of TATA-binding pro
โœ Patterson, George H.; Schroeder, Stephanie C.; Bai, Yu; Weil, P. Anthony; Piston ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 188 KB ๐Ÿ‘ 2 views

We describe the quantitative monitoring of TATA-binding protein (TBP) localization and expression in living Saccharomyces cerevisiae cells. We replaced the endogenous TBP with a green fluorescent protein (GFP) โ€ข TBP fusion, which was imaged quantitatively by laser scanning confocal microscopy (LSCM)