Advanced Photoperiod and Water Temperature Effects on Gill Na+–K+ Adenosine Triphosphatase Activity and Migration of Juvenile Steelhead (Salmo gairdneri)

1981 ◽  
Vol 38 (7) ◽  
pp. 758-764 ◽  
Author(s):  
W. S. Zaugg

Under raceway conditions, an advanced photoperiod schedule caused migratory movements and elevation in gill Na+–K+ adenosine triphosphatase activity (Na+–K+ ATPase) to occur about 1 mo earlier than normal in yearling summer steelhead (Salmo gairdneri) from Dworshak National Fish Hatchery (Idaho). Exposure of migrants to 13 °C for 20 d resulted in serious impairment of continued migratory behavior and a reduction of gill Na+–K+ ATPase activity. Migrants outnumbered nonmigrants at fork lengths of 16 cm and longer. It is proposed that the potentially detrimental effects of warming river temperatures during the normal migratory season and delayed migration caused by dams and impoundments might be partially overcome by inducing early smolt transformation and migration with the use of advanced photoperiods.Key words: ATPase, steelhead, migration, temperature, photoperiod, smolts

1977 ◽  
Vol 162 (3) ◽  
pp. 665-670 ◽  
Author(s):  
F Gibson ◽  
G B Cox ◽  
J A Downie ◽  
J Radik

A plasmid was isolated which included the region of the Escherichia coli chromosome carrying the known genes concerned with oxidative phosphorylation (unc genes). This plasmid was used to prepare partial diploids carrying normal unc alleles on the episome and one of the three mutant alleles (unc A401, uncB402 or unc-405) on the chromosome. These strains were compared with segregants from which the plasmid had been lost. Dominance of either normal ormutant unc alleles was determined by growth on succinate, growth yields on glucose, Mg-ATPase (Mg2+-stimulated adenosine triphosphatase) activity, atebrin-fluorescence quenching, ATP-dependent transhydrogenase activity and oxidative phosphorylation. In all the above tests, dominance of the normal allele was observed. However, in membranes from the diploid strains which carried a normal allele and either of the mutant alleles affecting Mg-ATPase activity (uncA401 or unc-405), the energy-linked functions were only partially restored.


1980 ◽  
Vol 137 (4) ◽  
pp. 343-345 ◽  
Author(s):  
L. J. Whalley ◽  
M. Scott ◽  
H. W. Reading ◽  
J. E. Christie

SummaryErythrocyte membrane adenosine triphosphatase activities were examined in twelve unipolar depressed patients receiving ECT. Eleven patients undergoing diagnostic cystoscopy served as controls for the acute effects of anaesthesia, and sixteen healthy subjects served as non-depressed controls. The unipolar depressed patients had a slight reduction in their (Na++K+)-ATPase activity but effective ECT treatment was not associated with any increase in this activity. This approach is unlikely to cast further light on the membrane phenomenology of depressive illness.


1981 ◽  
Vol 200 (3) ◽  
pp. 655-661 ◽  
Author(s):  
P N Lowe ◽  
R B Beechey

Chloroform-released ATPase from ox heart mitochondria contains significant amounts of inhibitor protein. There is a correlation between processes that affect the interactions between the inhibitor protein and the ATPase molecule and the ability of MgATP to induce an inhibition of ATPase activity. Evidence is presented suggesting that the endogenous inhibitor protein is involved in the process of MgATP-induced inhibition of soluble ATPase activity.


1974 ◽  
Vol 52 (7) ◽  
pp. 871-877 ◽  
Author(s):  
I. A. Johnston ◽  
S. Patterson ◽  
P. Ward ◽  
G. Goldspink

A technique for the demonstration of myofibrillar adenosine triphosphatase activity (ATPase) used for mammalian muscle has been modified to suit fish muscle. The mammalian method involves selectively inhibiting fiber types by preincubation at either alkaline (pH 10.4) or acid (pH 4.3) pH before incubation for myofibrillar (ATPase) activity. Fish muscle fibers were found to be generally inactivated under these conditions. Preincubation at an acid pH was found to be unsuitable for fish muscle because of the indiscriminate inactivation of the fibers. The effects of preincubating at pH 10.4 and incubating tissue sections for different time periods and at different pH's and temperatures have been investigated. A differential staining of fiber types correlated with biochemical data on myofibrillar ATPase for red and white muscles was obtained by preincubating sections for short periods (1–2 min) at pH 10.4. Under these conditions the intermediately positioned pink fibers were found to stain similarly to the white fibers of high myofibrillar ATPase activity. An investigation has been made of the qualitative distribution of fiber types in the myotomal muscle of live teleost species: coalfish (Gadus virens), grey mullet (Mugil cephalus), crucian carp (Carassius carassius), black mollie (Mollienesia sp), and glassfish (Chanda ranga). The pink fibers were found to be abundant in all the species examined with the exception of the glassfish.


1962 ◽  
Vol 10 (6) ◽  
pp. 731-740 ◽  
Author(s):  
D. NAIDOO

The location of adenosine triphosphatase in the brain has been studied in rapidly frozen-dried cerebral tissues of the Wistar rat. It is found that adenosine triphosphatase is an almost exclusively nuclear enzyme. Two tissue fractions of the cerebrum were separated, so that one sample was made up of vascular elements, and the other of neural elements. The two fractions were then studied for their adenosine triphosphatase activity, and compared with the histochemical findings. The two tissue fractions were found not to differ in the absence of bivalent cations. When Ca++ were added to the cerebral vascular suspension, ATPase activity was increased approximately 15 times, and only 3 times in the presence of Mg++. Conversely, the addition of Mg++ increased the ATPase activity of the neural fraction 200%; whereas, Ca++ was responsible for a 60% increase. This fact was detectable microscopically when Ca++ was found to intensify vascular nuclear staining, and Mg++ to increase the neuronal and glial nuclear staining. The results, histochemical and biochemical, are mutually confirmatory.


1973 ◽  
Vol 19 (10) ◽  
pp. 1265-1267 ◽  
Author(s):  
Z. Vaituzis

Cytochemical studies on motile bacteria revealed magnesium-dependent adenosine triphosphatase (ATPase) activity at the membranous sites of flagellar origin. The studies were done on bacteria representing three types of flagellation, namely, peritrichate, lophotrichate, and monotrichate. Escherichia coli and S. serpens showed a uniform distribution of ATPase reaction products throughout the periplasmic space. In B. licheniformis and V. metchnikovii the reaction products were found in the cytoplasm accumulated in areas where flagella originate.


1979 ◽  
Vol 183 (2) ◽  
pp. 475-476 ◽  
Author(s):  
A Ferri ◽  
E Magri ◽  
E Grazi

The release of Pi from the Pi-G-actin-ADP complex is the rate-limiting step in the ATPase activity that is shown by ATP-G-actin in the presence of protamine.


1972 ◽  
Vol 29 (2) ◽  
pp. 167-171 ◽  
Author(s):  
W. S. Zaugg ◽  
L. R. McLain

The average Na+- and K+-stimulated adenosinetriphosphatase (ATPase) activity of microsomes from gills of hatchery-reared coho salmon (Oncorhynchus kisutch) increased from about 12 μmoles ATP hydrolyzed/mg protein per hr during February through mid-April to approximately 24 in mid-May. Larger fish developed higher activities than smaller fish. Hatchery-reared spring chinook salmon (O. tshawytscha) exhibited a similar increase 2–3 weeks earlier.In 2-year-old hatchery-reared steelhead trout (Salmo gairdneri), Na+-, K+-ATPase activities were elevated in some, but not all, smolt-appearing animals. Parr-appearing fish, including maturing males, showed no activity increase. When held in fresh water to July, steelhead smolts lost their silvery color and became more parr-like in appearance, and the previously elevated ATPase activity decreased to near pre-smolt levels. Yearling steelhead held at the laboratory showed a more consistent rise in ATPase activity.The increase in transport ATPase (Na+-, K+-stimulated) activity occurring during parr–smolt transformation is probably a preparatory step for saltwater adaption and may also be closely associated with migratory disposition.L'activité moyenne de l'adénosinetriphosphatase (ATPase) stimulée par Na+ et K+ dans les microsomes des branchies de saumons coho (Oncorhynchus kisutch) élevés en pisciculture augmente de 12 μmoles environ d'ATPase hydrolysée/mg de protéine par h de février à la mi-avril à 24 à la mi-mai. Les gros poissons développent une activité plus grande que les petits. Les saumons chinook de printemps (O. tshawytscha) élevés en pisciculture font preuve d'un accroissement semblable deux à trois semaines avant les saumons coho.


1974 ◽  
Vol 52 (7) ◽  
pp. 805-812 ◽  
Author(s):  
Harry H. Wagner

As evidenced by immediate-transition experiments, seawater adaptation in juvenile steelhead trout was independent of photoperiod and the onset of parr–smolt transformation. Increased survival occurred as the fish grew larger, and euryhalinity was reached at 12 to 13 cm. There was no marked regression in the hypoosmoregulatory mechanism in the summer. The regression reported in earlier studies was discussed in terms of seasonal changes in lipid reserves and Na+- and K+-activated adenosine triphosphatase (ATPase) activity in gill microsomes.


1971 ◽  
Vol 19 (2) ◽  
pp. 75-84 ◽  
Author(s):  
BERNARD D. TUNIK

The calcium precipitation method was used in an attempt to localize myofibrillar adenosine triphosphatase (ATPase) activity within the sarcomeres of single, unfixed, glycerol-extracted fibers from the pectoralis major muscle of leghorn chicks. ATPase was apparently present in only the A-I overlap region of unshortened fibers, and was apparently present in only the contraction bands of shortened fibers. The results are shown to be self-contradictory in view of the known submicroscopic morphology of the sarcomeres. However, the usual classical controls provided no evidence of artifactual localization. In a novel control, separate solutions of calcium and phosphate were caused to diffuse simultaneously into a fiber. The resulting precipitate was localized in patterns indistinguishable from those obtained from incubation of shortened or unshortened fibers in ATP. These patterns result from the localization of precipitate in regions of high protein concentration. Caution in interpreting the results of cytochemical procedures even though controls provide no evidence of artifactual localization is urged.


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