Effect of naphthalene and aqueous crude oil extracts on the green flagellate Chlamydomonas angulosa. V. Heterotrophic responses

1982 ◽  
Vol 60 (8) ◽  
pp. 1495-1502 ◽  
Author(s):  
J. A. Hellebust ◽  
C. Soto ◽  
T. C. Hutchinson

Chlamydomonas angulosa shows a relatively weak capacity for heterotrophic growth on acetate in the dark. The cell doubling time on acetate in the dark is about 62 h as compared with about 17 h for growth in the absence of acetate under optimal light conditions. The cell's capacity for acetate uptake and its isocitrate lyase activity are also relatively low. No [14C]glucose is taken up by the cells, in agreement with the inability of C. angulosa to grow on glucose in the dark or of glucose to stimulate growth under light-limiting conditions. The Km and Vmax for acetate uptake for cells cultured on 12 h light: 12 h dark cycle, at the end of a 12-h dark period, are 0.05 mM and 1.3 fmol cell−1 min−1, respectively. The uptake capacity increases strongly upon dark incubation, while the presence of light during short uptake experiments enhances the uptake rate. There is only a moderate 2.5 times increase in isocitrate lyase activity upon incubation of light-grown cells in the dark with acetate.Cells incubated in 100% naphthalene-saturated media undergo a rapid and complete loss of acetate uptake capacity. Media, 50% saturated with naphthalene or 100% saturated with aqueous crude oil extracts, cause an initial stimulation of acetate uptake. Media, 50% saturated with aqueous crude oil extracts cause a much longer (at least 7 days) stimulation of acetate uptake capacity. Similarly, 50% saturated-naphthalene media cause an increase in isocitrate lyase activity on a per cell basis over control cells. While 50% naphthalene-saturated media permit almost no cell division in closed acetate-containing cultures in the dark, very dramatic increases in cell size occur over long time periods. Moderate concentrations of crude oil components dissolved in algal culture media, thus, permit significant rates of acetate uptake and assimilation but inhibit cell division. It is possible that the observed stimulation of acetate uptake by moderate concentrations of crude oil components is due to the following reasons: (i) hydrocarbon-induced permeabilization of the cell membrane and (ii) an increased availability of energy from photosynthetic light reactions owing to decreased CO2 photoassimilation.


1985 ◽  
Vol 63 (4) ◽  
pp. 834-840 ◽  
Author(s):  
J. A. Hellebust ◽  
C. Soto ◽  
T. C. Hutchinson

Chlamydomonas angulosa grows equally well on nitrate and ammonium as sources of nitrogen. The presence of ammonium decreases nitrate uptake by less than 10% in short-term experiments. The presence of nitrate has no significant effect on short-term uptake of the ammonium analogue methylamine. Cells grown in nitrate media possess considerable methylamine uptake capacity during early exponential growth. This uptake capacity falls rapidly as the cells enter the declining growth phase. When cells are transferred to nitrogen-deficient media, the uptake capacity for methylamine increases threefold to fourfold in 24 h. The half-saturation constants (Km) for nitrate and methylamine uptake of this alga are 0.4 mM and 90 μM, respectively. When C. angulosa cells are transferred from control Bolds basal medium (BBM) to 50% naphthalene saturated or aqueous crude oil saturated media, the initial uptake rate for nitrate increases by a factor of two or decreases by a factor of one-third, respectively, as compared with that of cells transferred to control BBM. However, cells incubated in closed incubation systems with naphthalene or aqueous crude oil saturated media for 3 days lose nitrate when resuspended in control media. Cells transferred to media containing naphthalene up to 20% saturation show no immediate decrease in methylamine transport, while higher naphthalene concentrations cause an immediate decrease in transport activity. However, cells incubated in 50% naphthalene saturated media in a closed system for 2–4 h actually show increased methylamine transport activity when the incubation system is opened to allow escape of the hydrocarbon. Prolonged exposure to 50% naphthalene saturated media, however, causes progressive loss of transport activity.



1983 ◽  
Vol 66 (6) ◽  
pp. 1232-1236 ◽  
Author(s):  
M.C. Albizzatti de Rivadeneira ◽  
M.C. Manca de Nadra ◽  
A.A. Pesce de Ruiz Holgado ◽  
G. Oliver


1996 ◽  
Vol 199 (2) ◽  
pp. 337-349 ◽  
Author(s):  
K A Hammond ◽  
K C Lloyd ◽  
J Diamond

Using lactation in mice as a model, we sought to determine whether ceilings on sustained energy expenditure reside in the capacities of energy-acquiring and input organs (such as the intestine) or of energy-expending and output organs (such as the mammary glands). To distinguish between these possibilities experimentally, we surgically varied the teat number of lactating mother mice while simultaneously varying their litter size. The energy burden on each teat (i.e. the pup/teat ratio) could thus be varied independently of the energy burden (i.e. litter size) on the mother herself or on her intestine. At each teat number, pup mass proved to be maximal at intermediate litter sizes. At a given pup/teat ratio, mothers with five teats weaned pups no larger than the pups of normal (10-teat) mothers, even though the total energy burden on the former mothers was only half as large. Mothers with only two teats could not wean any pups. Litter size controlled maternal food intake, which in turn controlled intestinal mass and nutrient uptake capacity. Disproportionately high food intake for the smallest litters appears to reflect capital start-up costs of lactation. Pup mass is evidently limited by inadequate suckling stimulation of mammary glands.



1972 ◽  
Vol 46 (2) ◽  
pp. 605-609 ◽  
Author(s):  
Andrew Sivak ◽  
Brooke T. Mossman ◽  
B.L. Van Duuren


1978 ◽  
Vol 24 (2) ◽  
pp. 149-153 ◽  
Author(s):  
T. M. Lakshmi ◽  
Robert B. Helling

Levels of several intermediary metabolites were measured in cells grown in acetate medium in order to test the hypothesis that the glyoxylate cycle is repressed by phosphoenolpyruvate (PEP). Wild-type cells had less PEP than either isocitrate dehydrogenase – deficient cells (which had greater isocitrate lyase activity than the wild type) or isocitrate dehydrogenase – deficient, citrate synthase – deficient cells (which are poorly inducible). Thus induction of the glyoxylate cycle is more complicated than a simple function of PEP concentration. No correlation between enzyme activity and the level of oxaloacetate, pyruvate, or citrate was found either. Citrate was synthesized in citrate synthase – deficient mutants, possibly via citrate lyase.



Author(s):  
Jing Wen ◽  
Chun Li ◽  
Jinlai Feng ◽  
Chunlei Dai ◽  
Jungang Li ◽  
...  
Keyword(s):  


Mechanisms of action of cytokinins at the cellular and molecular levels are still unknown. Biological functions of cytokinins are presented through specific bioassay systems which are regarded as standard (delay of senescence of leaf tissue and stimulation of cell division) and which have been or may be biochemically investigated. These ‘biochemical functions’ of cytokinins are reviewed. The biochemical significance of the specific occurrence of cytokinins in transfer RNA molecules is discussed with respect to the question of the incorporation of labelled cytokinins into RNA molecules. Also, the significance of the cytokinin binding protein recently isolated from higher plant ribosomes is discussed.



Weed Science ◽  
1970 ◽  
Vol 18 (5) ◽  
pp. 565-571
Author(s):  
J. A. Mulliken ◽  
C. A. Kust ◽  
L. E. Schrader

Endosperm dry weight, protein, and fat losses accompanied rapid radicle growth of velvetleaf (Abutilon theophrasti Medic.) between 12 and 36 hr of germination at 31 C. Cotyledonary reserves were mobilized after 36 hr. Isocitrate lyase activity sedimented with a particulate fraction in varying degrees, but maximal activity developed at times coincident with fat mobilization. Respiration of excised endosperms reached maximal rates shortly after radicle emergence. The actions of hydrogen cyanide, carbon monoxide, and 2,4-dinitrolphenol indicated that respiration of endosperms excised from imbibed and germinated seed was due to cytochrome oxidase activity, and was coupled to phosphorylation.



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