๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Growth and cytochrome c oxidase activity in minute mutants ofDrosophila

โœ Scribed by Farnsworth, M. W.


Publisher
John Wiley and Sons
Year
1965
Tongue
English
Weight
572 KB
Volume
160
Category
Article
ISSN
0022-104X

No coin nor oath required. For personal study only.

โœฆ Synopsis


Total soluble protein present in 48-, 60-and 72-hour larval stages of Drosophik melanogaster was determined for controls and for heterozygotes of the following Minute mutants: M(2)1, M(2)173, M(2)z, M(2)S-10, M(3)w, M(3)124, M(3)B2, M(3)y and M ( 3 ) l . Cytochrome c oxidase activity was also assayed at these stages of development in mitochondria isolated from whole larvae of each genotype.

The results indicate that all of these mutants possess a common retardation in the rate of growth throughout the larval period. The different Minutes, however, each had distinctive growth patterns, often characterized by particular lags occurring at specific stages. The concentration of cytochrome c oxidase was not necessarily lowered in conjunction with periods of especially retarded growth, but instead, activity higher than that of the control was frequently found. Only one mutant of those tested, M(2)z, showed a significantly lower concentration of this enzyme.


๐Ÿ“œ SIMILAR VOLUMES


Regional brain variations of cytochrome
โœ C. Strazielle; K. Hayzoun; M. Derer; J. Mariani; R. Lalonde ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 446 KB

## Abstract Cell malpositioning has been described in laminated structures of the spontaneous mutation, __reeler__, including the cerebellum, the hippocampus, and the neocortex. Despite the ectopic positions of different neuronal populations, the specificity of synaptic connections is maintained. T

Residual muscle cytochrome c oxidase act
โœ Gabriele Siciliano; Bruno Rossi; Laura Manca; Corrado Angelini; Alessandra Tessa ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 634 KB

The data from histological, biochemical, and mitochondrial DNA (mtDNA) studies of muscle biopsies from 10 patients affected with chronic progressive external ophthalmoplegia (CPEO) were related to dynamic and metabolic parameters of incremental submaximal exercise. Maximum power output was reduced i