scholarly journals Formation of Starch in Isolated Chloroplasts

1958 ◽  
Vol 71 (844) ◽  
pp. 326-334 ◽  
Author(s):  
Rikizo UEDA
1960 ◽  
Vol 235 (3) ◽  
pp. 832-839 ◽  
Author(s):  
M. Losada ◽  
A.V. Trebst ◽  
Daniel I. Arnon

1984 ◽  
Vol 39 (6) ◽  
pp. 627-633 ◽  
Author(s):  
Ji-yu Ye ◽  
U. Heber

The effect of aureomycin on photosynthesis was investigated. This antibiotic which has been reported to stimulate photosynthesis at very low concentrations is an effective inhibitor at higher concentrations. In mesophyll protoplasts and isolated chloroplasts from spinach, 50% inhibition of CO2 reduction required about 20 μᴍ aureomycin. The reduction of 3-phosphoglycerate and of oxaloacetate by intact chloroplasts was also inhibited, but not that of nitrite and methylviologen which was actually stimulated. NADP reduction by broken chloroplasts and methylviologen- dependent photophosphorylation were also sensitive to aureomycin. The electrochromic shift at 518 nm which indicates formation of a light-dependent membrane potential was suppressed in the presence of 200 μᴍ aureomycin and the transthylakoid proton gradient was decreased. The data confirm reports that aureomycin has uncoupling properties, and they indicate that it also acts as an inhibitor of ferredoxin/NADP reductase.


1956 ◽  
Vol 69 (814) ◽  
pp. 202-206 ◽  
Author(s):  
Hayashi ONO ◽  
Yoso KONAGAMITSU

2021 ◽  
Vol 12 ◽  
Author(s):  
Jinjie An ◽  
Xin Miao ◽  
Lulu Wang ◽  
Xu Li ◽  
Xiaomin Liu ◽  
...  

Chloroplasts are essential organelles in plant cells with many important functions. Chloroplasts isolated by Percoll density gradient centrifugation are widely used in the study of chloroplasts. The intactness of isolated chloroplasts is necessary for many of the experiments. In the past, those isolated chloroplasts were either simply believed to be intact or had to be analyzed by indirect biochemical methods. Here we show a new method to check the intactness of isolated chloroplasts by staining their envelope with fluorescent dyes, Rhodamine or Nile red, and then observing them with a fluorescence microscope. With this method, broken chloroplasts and intact chloroplasts can be distinguished easily and their integrity can be checked in a few minutes. Results of this method agreed well with those of biochemical methods. Moreover, we have also found that sometimes the middle layer chloroplasts from the Percoll gradient centrifugation could be mostly broken, which could cause mistakes in the experiment. With our method, this problem can be easily found. This chloroplast envelope staining method can be used in the preparation of isolated chloroplasts to ensure the intactness.


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