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Chlamydomonas reinhardii

Irmer, U., I. Wachholz, H. Schafer, and D.W. Lorch. 1986. Influence of lead on Chlamydomonas reinhardii Danegard (Volvocales, Chlorophyta) accumulation, toxicity and ultrastructural changes. Environ. Exper. Bot. 26 97-105. [Pg.334]

Day, K. and N.K. Kaushik. 1987b. The adsorption of fenvalerate to laboratory glassware and the alga Chlamydomonas reinhardii, and its effect on uptake of the pesticide by Daphnia galeata mendotae. Aquat. Toxicol. 10 131-142. [Pg.1128]

Day, K. and N.K. Kaushik. 1987c. Short-term exposure of zooplankton to the synthetic pyrethroid, fenvalerate, and its effects on rates of filtration and assimilation of the alga, Chlamydomonas reinhardii. Arch. Environ. Contam. Toxicol. 16 423-432. [Pg.1128]

K.S. Kan and J.P. Thomber, Hie light-harvesting chlorophyll a/b-protein complex of Chlamydomonas reinhardii, Plant Physiol. 57 (1976)47-52. [Pg.288]

Ish-Shalom, D. and Ohad, I. 1983. Organization of chlorophyll-protein complexes of photosystem I in Chlamydomonas reinhardii. Biochim. Biophys. Acta 722,498-507. [Pg.164]

Grove TZ, Kostic NM. Metalloprotein association, self-association, and dynamics governed by hydrophobic interactions simultaneous occurrence of gated and true electron-transfer reactions between cytochrome and cytochrome c6 from Chlamydomonas reinhardii. J Am Chem Soc 2003 125 10598-607. [Pg.225]

In one respect, the variable-yield model has been a disappointment in the sense that it was hoped that the transient behavior of its solutions would better fit the transient behavior seen in experiments with certain algae [CNIJ. The experiments, described in [CM], involved the growth of a Chlamydomonas reinhardii population on a nitrogen substrate. Following a step increase in the dilution rate, damped oscillations were observed in cell numbers. Cunningham and Nisbet [CNl] note that the singlepopulation variable-yield model could not reproduce these oscillations without the introduction of time delays into the equations. See also the monograph [NG]. [Pg.207]

CM] A. Cunningham and P. Mass (1978), Time lag and nutrient storage effects in the transient growth response of Chlamydomonas reinhardii in nitrogen limited batch and continuous culture, Journal of General Microbiology 104 227-31. [Pg.300]

The ESR signal of Af, 2 could be observed in membrane preparation from a strain of Chlamydomonas reinhardii lacking PSI. The broad peak at g = 1.84 is again similar to what observed in bacterial RC and suggests a plastoquinone-Fe complex [87]. Also similar is the inhibitory effect of o-phenanthroline [88]. [Pg.115]

Feeding regime Various combinations of trout chow, yeast, rye grass powder, and algae have been used types of algae include Ankistrodesmus convolutus, A. falcatus, Chlamydomonas reinhardii, and Selenastrum capricomutum... [Pg.77]

Hydroxyprolyl glycopeptides have also been found in lower plants such as ferns and algae (Lamport and Miller, 1972). In the green algae Chlamydomonas reinhardii the pattern of glycosylation is different (O Neill... [Pg.112]

Similarly, chemotactic behaviour of bacteria is controlled by Ca . Mobile bacteria swim towards certain chemicals and away from others. Such bacteria can swim smoothly in a straight line or tumble, which results in random changes in direction. When heading towards repellents bacteria tumble more frequently to increase the probability of swimming away. Influx of Ca causes tumbling. Such behaviour has been found for Bacillus subtilis but apparently not for E. co/i. Calcium accelerates the swimming speed of Chlamydomonas reinhardii and regulates reverse motion in phototactically active Phormidium uncinatum and Halobacterium halobium. Phototaxis in H. halobium involves a methylation-demethylation process which is calcium dependent. Attractant stimuli raise the level of methylation of membrane proteins, while repellent stimuli cause demethylation and the enhanced opportunity for reversal of direction. Ca " " deactivates the methyl transferase and activates a methyl esterase. ... [Pg.6740]

Modes of Herbicide Action as Determined with Chlamydomonas reinhardii and Coulter Counting... [Pg.231]

Synchronously grown Chlamydomonas reinhardii cells were used for the differentiation between different physiological modes of herbicide action. The cells were counted with a Coulter Counter and the volume spectrum was obtained by an adapted Channelyzer,... [Pg.231]

Herbicide Metabolic pathway or process affected Chlamydomonas reinhardii I -values ijM) Growth Flagella regeneration ... [Pg.237]

Table III. Influence of herbicides that interfere with photosynthetic processes on growth and multiplication of Chlamydomonas reinhardii. The algae were kept in a synchronized 12/12 h light/dark cycle, with Oh at the beginning of a dark phase. Table III. Influence of herbicides that interfere with photosynthetic processes on growth and multiplication of Chlamydomonas reinhardii. The algae were kept in a synchronized 12/12 h light/dark cycle, with Oh at the beginning of a dark phase.
Table V. Action of 37 yuM alachlor on Chlamydomonas reinhardii growth and multiplication when present for different time-intervals during the growth cycle. Inoculation was with stationary algae with a cell volume of 90, um. Light phases were from 0-10, 24 - 3A and 48 - 58 h. C = Control, A = alachlor-treated. Table V. Action of 37 yuM alachlor on Chlamydomonas reinhardii growth and multiplication when present for different time-intervals during the growth cycle. Inoculation was with stationary algae with a cell volume of 90, um. Light phases were from 0-10, 24 - 3A and 48 - 58 h. C = Control, A = alachlor-treated.
Nultsch, W., Throm, G., and Rimscha, J. (1971) Phototaktische Lfntersuchungen an Chlamydomonas reinhardii Dangeard in homokontinuierHcher Kultur. Arch. Microbiol. 80, 351-369. [Pg.63]


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See also in sourсe #XX -- [ Pg.76 , Pg.96 , Pg.113 ]

See also in sourсe #XX -- [ Pg.226 ]

See also in sourсe #XX -- [ Pg.298 ]




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