Role of calcium and calmodulin antagonist in photosynthesis and salinity tolerance inChlorella vulgaris

1993 ◽  
Vol 35 (2) ◽  
pp. 237-244 ◽  
Author(s):  
R. Abdel-Basset
2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Deo Rashmi ◽  
Vitthal T. Barvkar ◽  
Altafhusain Nadaf ◽  
Swapnil Mundhe ◽  
Narendra Y. Kadoo

Planta ◽  
2020 ◽  
Vol 251 (5) ◽  
Author(s):  
Ali Kiani-Pouya ◽  
Fatemeh Rasouli ◽  
Lana Shabala ◽  
Ayesha T. Tahir ◽  
Meixue Zhou ◽  
...  

1994 ◽  
Vol 267 (4) ◽  
pp. F624-F631 ◽  
Author(s):  
M. Lu ◽  
L. E. Barber ◽  
J. L. Renfro

The role of apical membrane electrical potential, the possibility of K+ channel involvement, and the role of extracellular Ca2+ in transepithelial P(i) secretion were examined in primary monolayer cultures of flounder renal proximal tubule cells in Ussing chambers. Exposure to 200 nM thapsigargin (TG) significantly increased net P(i) secretion. In TG-stimulated tissues, substitution of 100 mM KCl for 100 mM NaCl in the luminal medium depolarized the apical membrane potential from -64 +/- 2.8 to -26 +/- 3.9 mV and strongly inhibited net P(i) secretion. In 32P(i)-preloaded tissues, cell-to-lumen exit of 32P(i) was significantly decreased to approximately 50% of control by high luminal K+ while cell-to-peritubular bath movement was unchanged. Addition of BaCl2 (2 mM) or charybdotoxin (20 nM) to the luminal surface significantly reduced TG-stimulated net P(i) secretion. The elevation of bath Ca2+ from 2 to 5 mM significantly increased secretory flux and decreased reabsorptive flux. The effect of TG on net P(i) secretion was reduced by the Ca2+ channel blocker verapamil (VE, 100 microM) to 65% of control and by calmodulin antagonist W-7 (20 microM) to 35% of control but it was not blocked by the protein kinase inhibitor H-7 (100 microM). VE also significantly inhibited the P(i) secretion induced by acidification of the peritubular bathing medium. The data indicate that transepithelial P(i) secretion induced by TG is significantly influenced by apical membrane electrical polarity, which may be regulated in part by Ca(2+)-activated K+ channels.


1990 ◽  
Vol 68 (4) ◽  
pp. 707-715 ◽  
Author(s):  
James Duston ◽  
Richard L. Saunders

Potential yearling (1+) smolts were maintained under 8.25 h light: 15.75 h dark and constant temperature (10.0 °C) from late December. Groups were subjected to an abrupt increase to 16 h light: 8 h dark on December 31 (group A), February 1 (group B), March 1 (group C), or March 31 (group D). Group E was maintained under constant 8.25 h light: 15.75 h dark for the duration of the experiment and group LDN was maintained under a simulated natural photoperiod cycle (45°N). Plasma osmolality levels following 24-h, 29‰ salinity challenge tests indicated a photoperiod-independent development of hypoosmoregulatory mechanisms preceding completion of smoltification that was significantly correlated with fish body size. As judged by 96-h, 37.5‰ salinity tolerance tests and changes in condition factor, completion of smolting occurred in sequence; in groups A and B it was advanced to late February, while groups C and D completed smolting in mid-March and mid-April, respectively, compared with late May for group LDN. Group E, maintained under constant 8.25 h light: 15.75 h dark, developed salinity tolerance in late May, but unlike other groups exhibited no large reduction in condition factor. Following smolting, an increase in condition factor and a loss of salinity tolerance occurred in all groups. The results support the hypothesis that changes in photoperiod entrain an endogenous circannual rhythm involved in controlling the completion of smoltification and subsequent loss of some smolt characteristics.


2011 ◽  
Vol 16 (11) ◽  
pp. 614-623 ◽  
Author(s):  
Richard P. Jacoby ◽  
Nicolas L. Taylor ◽  
A. Harvey Millar

2019 ◽  
Vol 117 ◽  
pp. 103899 ◽  
Author(s):  
María Botella-Cruz ◽  
Susana Pallarés ◽  
Andrés Millán ◽  
Josefa Velasco

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