Model Analysis of the Apparent Saturation Kinetics of Purine Nucleobase Uptake in Cells co-Expressing Transporter and Metabolic Enzyme

Author(s):  
Satoru Suzuki ◽  
Katsuhisa Inoue ◽  
Ikumi Tamai ◽  
Yoshiyuki Shirasaka
Author(s):  
Deepak Sharma ◽  
Donny D. Licatalosi ◽  
Eckhard Jankowsky

Intervirology ◽  
1980 ◽  
Vol 13 (6) ◽  
pp. 357-363 ◽  
Author(s):  
Jana Hillova ◽  
Miroslav Hill

1989 ◽  
Vol 9 (1) ◽  
pp. 288-295
Author(s):  
S G Swartwout ◽  
A J Kinniburgh

Transcripts of the proto-oncogene c-myc are composed of a rapidly degraded polyadenylated RNA species and an apparently much more stable, nonadenylated RNA species. In this report, the extended kinetics of c-myc RNA turnover have been examined in rapidly growing cells and in cells induced to differentiate. When transcription was blocked with actinomycin D in rapidly growing cells, poly(A)+ c-myc was rapidly degraded (t1/2 = 12 min). c-myc RNA lacking poly(A) initially remained at or near control levels; however, after 80 to 90 min it was degraded with kinetics similar to those of poly(A)+ c-myc RNA. These bizarre kinetics are due to the deadenylation of poly(A)+ c-myc RNA to form poly(A)- c-myc, thereby initially maintaining the poly(A)- c-myc RNA pool when transcription is blocked. In contrast to growing cells, cells induced to differentiate degraded both poly(A)+ and poly(A)- c-myc RNA rapidly. The rapid disappearance of both RNA species in differentiating cells suggests that a large proportion of the poly(A)+ c-myc RNA was directly degraded without first being converted to poly(A)- c-myc RNA. Others have shown that transcriptional elongation of the c-myc gene is rapidly blocked in differentiating cells. We therefore hypothesize that in differentiating cells a direct, rapid degradation of poly(A)+ c-myc RNA may act as a backup or fail-safe system to ensure that c-myc protein is not synthesized. This tandem system of c-myc turnoff may also make cells more refractory to mutations which activate constitutive c-myc expression.


1997 ◽  
Author(s):  
Vladimir P. Zorin ◽  
Iosif S. Mikhalovsky ◽  
Tatyana E. Zorina
Keyword(s):  

1990 ◽  
Vol 45 (1-2) ◽  
pp. 71-73 ◽  
Author(s):  
Kiriakos Kotzabasis ◽  
Horst Senger

The intermediate of chlorophyll biosynthesis, 5-aminolevulinic acid (ALA ), is a necessary prerequisite for the formation of protochlorophyllide (PChlide) and protochlorophyll (PChl) in the dark. The application of ALA to a dark-grown culture of the pigment mutant C-2 A′ of Scenedesmus obliquus increased the amount of PChlide 30-fold and the amount of PChl about 10-fold. The rates of ALA-dependent formation of PChlide and PChl reach their maximum values at different concentrations of added ALA . Similarly, the kinetics of PChlide and PChl formation in cells incubated with ALA are different. Cells of Scenedesmus mutant C-2 A′ incubated with various concentrations of ALA for different periods provide a good tool for future studies differentiating between PChlide and PChl metabolism . − The incorporation of Chl deriving from either PChl or PChlide into different pigment protein complexes is discussed.


1988 ◽  
Vol 254 (4) ◽  
pp. G602-G609
Author(s):  
H. Vilstrup ◽  
L. T. Skovgaard

The kinetics of hepatic alanine uptake and urea synthesis in relation to sinusoid alanine concentration was investigated in seven anesthetized pigs weighing 63 kg, using liver vein catheterizations. Each experiment consists of four steady-state periods of 40 min with alanine concentrations in the range of 0.4-27 mmol/l. The process rates were measured as the products of transhepatic concentration gradients and hepatic blood flow rate, determined by indocyanine green. The data suggest that both processes follow saturation kinetics, that there exists a sinusoidal concentration of alanine below which net removal is limited, and that urea synthesis consists of two components: one alanine independent and one depending on alanine concentration according to Michaelis-Menten kinetics. The kinetic parameters were estimated iteratively by the maximum likelihood method. The maximum rate of alanine uptake was 1.13 +/- 0.74 mmol.min-1.kg liver wt-1 (mean +/- SD), the alanine concentration resulting in half-maximum alanine uptake rate was 1.69 +/- 0.99 mmol/l, and the removal-limiting alanine concentration was 0.27 +/- 0.09 mmol/l. The maximum rate of urea-N synthesis was 1.49 +/- 0.87 mmol.min-1.kg liver wt-1, the alanine concentration resulting in half-maximum urea-N synthesis rate was 2.32 +/- 1.11 mmol/l, and the alanine concentration-independent urea-N synthesis rate was 0.13 +/- 0.10 mmol.min-1.kg liver wt-1.


1985 ◽  
Vol 63 (3) ◽  
pp. 512-516
Author(s):  
J. R. Cumming ◽  
R. T. Eckert ◽  
L. S. Evans

Potassium uptake by roots of 3-week-old red spruce (Picea rubens Sarg.) seedlings was measured in nutrient solutions ranging in K+ concentration from 0.01 to 10.0 mM. Nonlinear least squares analysis was used to estimate uptake parameters Vmax and Km. Analyses of residuals generated by several theoretical models of ion uptake were undertaken to choose the best mechanistic uptake model. Potassium absorption by red spruce seedlings was characterized by Michaelis–Menten behavior from K+ solutions in the range 0.01 to 1.0 mM. Above 1.0 mM, accumulation of potassium was most readily accounted for by a linear diffusive component superimposed on saturation kinetics. Uptake parameter values of Vmax = 1.17 μmol K∙g fresh weight−1∙h−1 and Km = 0.083 mM were similar to those reported for other species. The culture of seedlings in full-strength nutrient solution did not reduce the ability to resolve these uptake parameters in short-term experiments.


Sign in / Sign up

Export Citation Format

Share Document