The association of gibberellin-like activity with the chloroplast fraction of leaf homogenates

Planta ◽  
1968 ◽  
Vol 81 (1) ◽  
pp. 106-112 ◽  
Author(s):  
J. L. Stoddart
Keyword(s):  
1971 ◽  
Vol 19 (1) ◽  
pp. 1 ◽  
Author(s):  
MJ Mercer ◽  
FV Mercer

Changes in the total nitrogen content of single internodal cells and in the nitrogen content of the cell wall, chloroplast fraction, TCA-insoluble cytoplasmic fraction, cytoplasmic sap, and vacuolar sap during the growth of the internodal cell are described. The nitrogen content of all fractions increases as the cells expand from c. 10 �l to over 200 �l in volume, and protein increases in the cytoplasm, the chloroplast fraction, and the cell wall. Cell wall nitrogen accounts for over half the total nitrogen of the cell and the bulk of the soluble nitrogen is present in the cytoplasm; only about 1% is found in the vacuole. The observations are discussed in relation to the cells of higher plants.


1966 ◽  
Vol 44 (4) ◽  
pp. 459-467 ◽  
Author(s):  
P. S. Sastry ◽  
M. Kates

Cell-free homogenates of spinach leaves incorporated glycerophosphate-32P into phosphatides when supplied with adenosine triphosphate, Mg++and coenzyme A (CoA). Most of the activity of the homogenate was associated with the microsome fraction sedimented at 104,000 × g, but some activity was also present in the chloroplast fraction. In all systems, most of the32P incorporated appeared in phosphatide acid (+ lysophosphatidic acid), with small to trace amounts in phosphatidyl glycerol and phosphatidyl inositol. Coenzyme A and adenosine triphosphate + Mg++were obligatory cofactors for the incorporation of α-glycerophosphate-32P but acetate + bicarbonate, cytidine triphosphate, or light were not essential. The results demonstrate the presence of acyl-CoA:L-glycerol-3-phosphate O-acyltransferase in the microsome fraction of spinach leaves and also indicate the existence of enzyme systems catalyzing the conversion of phosphatidic acid to phosphatidyl inositol and phosphatidyl glycerol.


1977 ◽  
Vol 55 (11) ◽  
pp. 1457-1464 ◽  
Author(s):  
S. C. Fry ◽  
R. G. S. Bidwell

First trifoliate leaves of wax beans. Phaseolus vulgaris, were exposed to 14CO2 in light for periods of 15 to 75 s. Leaves were frozen in liquid N2 and a chloroplast fraction was isolated nonaqueously. The chloroplast fraction contained a small amount of contaminating cytoplasm that could not be removed. Labelled photosynthetic compounds were separated from the whole leaves and from the corresponding chloroplast fractions and their radioactivity was measured.The compounds fell into two groups in their behaviour. Glyceric acid and ribulose, derived from photosynthetic 3-phosphoglyceric acid and ribulose diphosphate respectively, remained largely or exclusively in the chloroplast fraction. Labelled sucrose and serine and glycine, on the other hand, were located in the chloroplast fraction only during the first 15–30 s of 14CO2 supply, and appeared in the cytoplasmic fraction in increasing amounts thereafter. The results suggest that serine and glycine are produced in organelles in the layer of cytoplasm that closely surrounds the chloroplasts and is isolated with them in the non aqueous technique. Sucrose may also be synthesized from photosynthetic intermediates in this layer of cytoplasm. Sucrose was not formed from intermediates of the glycolate pathway in detached leaves.


1988 ◽  
Vol 253 (2) ◽  
pp. 533-539 ◽  
Author(s):  
T Saidha ◽  
S Q Na ◽  
J Y Li ◽  
J A Schiff

We have previously shown that a sulphate activating system is present on the outside of the inner mitochondrial membrane of Euglena gracilis Klebs. var. bacillaris Cori, but efforts to couple this system to ATP produced from oxidative phosphorylation were unsuccessful. In the present work we show that the concentration of Pi ordinarily used to support oxidative phosphorylation in these mitochondria (10 mM) inhibits sulphate activation completely; by reducing the concentration of Pi 10-fold, both processes proceeded normally. Sulphate activation under these conditions is inhibited nearly completely by the uncouplers of oxidative phosphorylation dinitrophenol (0.1 mM) and carbonyl cyanide m-chlorophenylhydrazone (CCCP) (0.2 microM). Sulphate reduction to form free cysteine, most of which appears outside the organelle, and in the cysteine of mitochondrial protein can be demonstrated in the same preparations, is membrane-bound and is inhibited by chloramphenicol (100 micrograms/ml), NaN3 (5 mM), KCN (100 microM); dinitrophenol (0.1 mM) or CCCP (0.2 microM). Digitonin fractionation of the mitochondria into mitoplasts, outer membranes and an intermembrane fraction show that reduction of 35SO4(2-) to form free cysteine and cysteine of protein is located on the mitoplasts; adenosine 5′-phosphosulphate sulphotransferase, the first enzyme of sulphate reduction, is found in the same location. Sulphate activation is highly enriched in the mitochondrial fraction of Euglena; the small amount found in the chloroplast fraction can be attributed to mitochondrial contamination. Thus, in Euglena, sulphate activation and reduction are contained in a sulphate metabolizing centre on the outside of the mitochondrial inner membrane; this centre appears to supply the mitochondrion and the rest of the cell with the products of sulphate activation as well as with reduced sulphur in the form of cysteine. Mitochondria from wild-type Euglena cells and from W10BSmL, a mutant lacking plastids completely, appear to be similar in the properties studied.


1952 ◽  
Vol 5 (2) ◽  
pp. 244 ◽  
Author(s):  
JG Wood ◽  
Pamela M Sibly

Throughout the life cycle of oat plants carbonic anhydrase activity, which is restricted to the non-chloroplast fraction of leaves, reaches a maximum value and then decreases. After appearance of deficiency symptoms carbonic anhydrase activity is less in zinc-deficient plants than in fully manured controls of the same age and is associated with a lower zinc content of the leaves.


1975 ◽  
Vol 14 (10) ◽  
pp. 2135-2139 ◽  
Author(s):  
Harmesh K. Sharma ◽  
Chelakara S. Vaidyanathan
Keyword(s):  

1960 ◽  
Vol 43 (6) ◽  
pp. 1083-1102 ◽  
Author(s):  
Hiroto Naora ◽  
Hatsuko Naora ◽  
Jean Brachet

1. The RNA content of anucleate and nucleate fragments of Acetabularia has been measured. It was found that there is a net synthesis of RNA in nucleate fragments. On the other hand, the RNA content of anucleate fragments did not change significantly after enucleation. 2. Anucleate fragments, however, can readily incorporate 14C-labeled adenine, orotic acid, and carbon dioxide into their cytoplasmic RNA. 3. The results of experiments on 14CO2 incorporation into the RNA of anucleate and nucleate fragments suggest that there is a mechanism for de novo synthesis of RNA in anucleate cytoplasm. 4. In Acetabularia, 81 per cent of the cytoplasmic RNA is bound to a large granule fraction, consisting mainly of chloroplasts. Even after removal of the nucleus, RNA is synthesized in this "chloroplast" fraction. The chloroplasts are thus a major site of RNA synthesis in the cytoplasm of these algae. Synthesis of "chloroplastic" RNA, in anucleate fragments, possibly occurs at the expense of the RNA present in other fractions (microsomes and supernatant). 5. 8-Azaguanine stimulates regeneration and cap formation in anucleate fragments and does not inhibit RNA synthesis in these fragments.


2015 ◽  
Vol 41 (2) ◽  
pp. 217-222 ◽  
Author(s):  
E. Mikulska ◽  
W. Maciejewska-Potapczyk ◽  
I. Konopska ◽  
B. Damsz

This paper deals with attempts to elaborate a simple method of spinach chloroplast isolation ensuring a high proportion of intact chloroplasts. We obtained 3 preparations of isolated chloroplasts. Several preliminary analyses of the obtained chloroplast fraction were also performed. Phosphorus compounds, total protein and the enzyme activities of RNase, DNase and GPase were determined. We found: 0,36-0,59% of RNA, 0,19-0,24% of DNA, 2,1-2,9% of phospholipids and 26-28% of protein. RNase activity was very high.


1969 ◽  
Vol 111 (4) ◽  
pp. 573-582 ◽  
Author(s):  
Jean G. Ebbon ◽  
G. H. Tait

1. An enzyme that methylates magnesium protoporphyrin was detected in extracts of light-grown and dark-grown cells of Euglena gracilis. The activity in light-grown cells is two to three times that in cells grown in the dark. 2. The activity is mainly located in the chloroplast fraction from light-grown cells and in proplastids in dark-grown cells. However, in cells grown either in the light or dark, about 15–20% is found in particle-free supernatant. 3. The chloroplast methylating enzyme was solubilized by the action of Tween 80 and partially purified. The properties were investigated. 4. From experiments in which etiolated cells were illuminated in the presence of inhibitors of chloroplast or cytoplasmic protein synthesis, it appears that the methylating enzyme is made on cytoplasmic ribosomes.


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