Effects of pH on cell morphology and carbonic anhydrase activity and localization in bloom-forming Mougeotia (Chlorophyta, Charophyceae)

2000 ◽  
Vol 78 (9) ◽  
pp. 1206-1214 ◽  
Author(s):  
Patricia Arancibia-Avila ◽  
John R Coleman ◽  
William A Russin ◽  
Lee W Wilcox ◽  
James M Graham ◽  
...  

A species of Mougeotia (C.A. Agardh) that was the dominant component of a metaphytic bloom-forming filamentous algal assemblage in an experimentally acidified lake (Little Rock Lake, Vilas County, Wisconsin, U.S.A.) was isolated into unialgal culture for analysis of pH effects on cell morphology and carbonic anhydrase activity and localization. External and total carbonic anhydrase activities at pH 8 were significantly greater than those at pH 5, but internal carbonic anhydrase activities were not significantly different at the two pH levels, as determined by use of a potentiometric technique. Ultrastructural immunogold labeling with a polyclonal antibody to Chlamydomonas periplasmic carbonic anhydrase suggested that an antigenically similar protein was located in the periplasmic space, inflated end walls, chloroplast, and peripheral cytoplasm of Mougeotia grown at both pH 8 and 5. Activity measurements and localization data were consistent with the hypothesis that a carbon concentration mechanism operates in this Mougeotia species at both high and low pH. Growth form, cell dimensions, chloroplast morphology, and cell wall ultrastructure were significantly different in cultures grown at pH 5 and pH 8. These structural and carbon acquisition features may contribute to Mougeotia's ability to form conspicuous metaphytic blooms in acidified waters.Key words: carbonic anhydrase, acidification, algal blooms, Mougeotia.

2000 ◽  
Vol 78 (9) ◽  
pp. 1206-1214 ◽  
Author(s):  
Patricia Arancibia-Avila ◽  
John R. Coleman ◽  
William A. Russin ◽  
Lee W. Wilcox ◽  
James M. Graham ◽  
...  

1984 ◽  
Vol 32 (6) ◽  
pp. 625-635 ◽  
Author(s):  
T Ikejima ◽  
S Ito

Mouse parotid gland and saliva were studied by histochemical, immunohistochemical, and activity measurements for carbonic anhydrase. Hansson 's histochemical reaction for carbonic anhydrase revealed positive enzyme activity in the parotid acinar cell cytoplasm and little or no reaction in the secretory granules. The luminal contents in all of the glandular duct systems also reacted positively, but the duct cells themselves were only weakly positive. Ultrastructural observations confirmed the light microscope histochemical localization and, in addition, revealed luminal content activity in intercellular ducts. Purified carbonic anhydrase isolated from mouse salivary glands was used to raise antibodies in rabbits. Localization of carbonic anhydrase by direct immunolabeling with fluorescein-coupled antibody and indirect immunoperoxidase labeling revealed enzyme localization on or in the acinar cell secretory granule membrane and not in the surrounding cytoplasm. The luminal contents of the intercalated and striated ducts were also strongly positive. Stimulation of salivary secretion with phenylephrine or pilocarpine increased the amount of carbonic anhydrase in saliva. Acetatazolamide and potassium cyanate inhibited carbonic anhydrase activity. Reasons underlying the discrepancy between the histochemical and immunolabeling localization of carbonic anhydrase are discussed. It is concluded that the parotid acinar cells of mice appear to be a significant source of carbonic anhydrase in saliva but its role is enigmatic.


2000 ◽  
Vol 203 (15) ◽  
pp. 2297-2310 ◽  
Author(s):  
J.M. Wilson ◽  
D.J. Randall ◽  
M. Donowitz ◽  
A.W. Vogl ◽  
A.K. Ip

The branchial epithelium of the mudskipper Periophthalmodon schlosseri is densely packed with mitochondria-rich (MR) cells. This species of mudskipper is also able to eliminate ammonia against large inward gradients and to tolerate extremely high environmental ammonia concentrations. To test whether these branchial MR cells are the sites of active ammonia elimination, we used an immunological approach to localize ion-transport proteins that have been shown pharmacologically to be involved in the elimination of NH(4)(+) (Na(+)/NH(4)(+) exchanger and Na(+)/NH(4)(+)-ATPase). We also investigated the role of carbonic anhydrase and boundary-layer pH effects in ammonia elimination by using the carbonic anhydrase inhibitor acetazolamide and by buffering the bath water with Hepes, respectively. In the branchial epithelium, Na(+)/H(+) exchangers (both NHE2- and NHE3-like isoforms), a cystic fibrosis transmembrane regulator (CFTR)-like anion channel, a vacuolar-type H(+)-ATPase (V-ATPase) and carbonic anhydrase immunoreactivity are associated with the apical crypt region of MR cells. Associated with the MR cell basolateral membrane and tubular system are the Na(+)/K(+)-ATPase and a Na(+)/K(+)/2Cl(−) cotransporter. A proportion of the ammonia eliminated by P. schlosseri involves carbonic anhydrase activity and is not dependent on boundary-layer pH effects. The apical CFTR-like anion channel may be serving as a HCO(3)(−) channel accounting for the acid-base neutral effects observed with net ammonia efflux inhibition.


2016 ◽  
Vol 18 (5) ◽  
pp. 600-612 ◽  
Author(s):  
Yudong Nie ◽  
Zhi Zhang ◽  
Qian Shen ◽  
Wenjin Gao ◽  
Yingfan Li

The relationships among carbonic anhydrase activity, algal cell density, and other environmental parameters have been investigated in Jialing River, which provide a new method of monitoring algal cell density and predicting algal blooms.


2004 ◽  
Vol 171 (4S) ◽  
pp. 296-296
Author(s):  
Michael Straub ◽  
Joséphine Befolo-Elo ◽  
Richard E Hautmann ◽  
Edgar Braendle

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