Optimum temperature and salinity conditions for growth of green algae Chlorella ellipsoidea and Nannochloris oculata

2007 ◽  
Vol 73 (5) ◽  
pp. 1050-1056 ◽  
Author(s):  
Sung Hwoan CHO ◽  
Sung-Choon JI ◽  
Sung Bum HUR ◽  
Jeanhee BAE ◽  
In-Seok PARK ◽  
...  
1998 ◽  
Vol 76 (6) ◽  
pp. 1072-1083 ◽  
Author(s):  
Yusuke Matsuda ◽  
Gale G Bozzo ◽  
Brian Colman

The regulation of the expression of the inorganic carbon concentrating mechanism (CCM) in aquatic photoautotrophs, particularly green algae, has been thought to require light and active photosynthesis. Recent studies, however, have indicated that there may be a light-independent pathway of signal transduction in green algae that may regulate the expression of CCMs in response to changes in ambient dissolved inorganic carbon (DIC) concentration. In the green alga, Chlorella ellipsoidea, changes in the rate of transport of both CO2 and HCO3- were shown to occur in response to the CO2 concentration in the bulk medium, independent of pH, whereas other inorganic carbon species, which might induce or repress DIC transport expression, were shown to change markedly with the pH of the medium. Furthermore, neither changes in the CO2 concentration around ribulose bisphosphate carboxylase-oxygenase (Rubisco) nor light were shown to be critical factors in regulating CCM expression in this alga. CO2-insensitive mutants of Chlorella ellipsoidea were recently isolated in which DIC transport operates constitutively at maximum activity. These results strongly suggest that a direct CO2 sensing mechanism may operate at the cell surface in Chlorella ellipsoidea and that this mechanism may trigger the repression of the expression of DIC transport in response to high CO2. Some supportive evidence for this hypothesis has also been obtained in other green algae, Chlamydomonas reinhardtii and Chlorella kessleri. The possibility of the occurrence of a direct sensing mechanism for CO2, its implications, and possible coexistence of other regulatory systems for CCM expression are discussed.Key words: green algae, Chlorella, signal transduction, CO2-insensitive mutants, CO2-sensing mechanism.


Author(s):  
L. V. Leak

Electron microscopic observations of freeze-fracture replicas of Anabaena cells obtained by the procedures described by Bullivant and Ames (J. Cell Biol., 1966) indicate that the frozen cells are fractured in many different planes. This fracturing or cleaving along various planes allows one to gain a three dimensional relation of the cellular components as a result of such a manipulation. When replicas that are obtained by the freeze-fracture method are observed in the electron microscope, cross fractures of the cell wall and membranes that comprise the photosynthetic lamellae are apparent as demonstrated in Figures 1 & 2.A large portion of the Anabaena cell is composed of undulating layers of cytoplasm that are bounded by unit membranes that comprise the photosynthetic membranes. The adjoining layers of cytoplasm are closely apposed to each other to form the photosynthetic lamellae. Occassionally the adjacent layers of cytoplasm are separated by an interspace that may vary in widths of up to several 100 mu to form intralamellar vesicles.


Author(s):  
A. E. Hotchkiss ◽  
A. T. Hotchkiss ◽  
R. P. Apkarian

Multicellular green algae may be an ancestral form of the vascular plants. These algae exhibit cell wall structure, chlorophyll pigmentation, and physiological processes similar to those of higher plants. The presence of a vascular system which provides water, minerals, and nutrients to remote tissues in higher plants was believed unnecessary for the algae. Among the green algae, the Chaetophorales are complex highly branched forms that might require some means of nutrient transport. The Chaetophorales do possess apical meristematic groups of cells that have growth orientations suggestive of stem and root positions. Branches of Chaetophora incressata were examined by the scanning electron microscope (SEM) for ultrastructural evidence of pro-vascular transport.


2015 ◽  
Vol 51 (4) ◽  
pp. 39-45
Author(s):  
N. I. Kirpenko ◽  
O. M. Usenko ◽  
T. O. Musiy

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