scholarly journals Structure and rearrangements of rRNA genes in chloroplast DNA in two strains of Euglena gracilis

1984 ◽  
Vol 3 (3) ◽  
pp. 127-136 ◽  
Author(s):  
Barbara Koller ◽  
Hajo Delius ◽  
Robert B. Helling
1968 ◽  
Vol 38 (1) ◽  
pp. 151-157 ◽  
Author(s):  
N. Steele Scott ◽  
Vinod C. Shah ◽  
Robert M. Smillie

Chloroplasts isolated from Euglena gracilis incorporated both tritiated thymidine 5'-triphosphate and tritiated deoxyadenosine 5'-triphosphate into an acid-stable fraction. The incorporation was dependent on the presence of all four deoxynucleoside triphosphates and was sensitive to treatment with deoxyribonuclease and actinomycin D. It was demonstrated that bacterial contamination could not account for the incorporation of label. Extraction of DNA from the chloroplasts and subsequent density gradient centrifugation of the DNA in CsCl2 showed that the incorporation was into chloroplast DNA (ρ = 1.686) of high molecular weight.


1990 ◽  
pp. 2397-2404
Author(s):  
Richard B. Hallick ◽  
David A. Christopher ◽  
Donald W. Copertino ◽  
Robert G. Drager ◽  
Ling Hong ◽  
...  

1993 ◽  
Vol 23 (2) ◽  
pp. 234-238 ◽  
Author(s):  
B. Karpinska ◽  
S. Karpinski

A physical map of Pinussylvestris L. chloroplast DNA for three restriction endonucleases (PstI, SacI, and KpnI) has been prepared by hybridization of isolated or cloned restriction fragments. Pinussylvestris chloroplast DNA is about 120 kilobases. Ten chloroplast genes have been localized by hybridization with heterologous chloroplast DNA probes. The genome contains single copies of the 23S and 16S rRNA genes and lacks any large repeated sequences. The restriction site arrangement and gene order have been compared with other known chloroplast DNA genetic maps of pine species.


FEBS Letters ◽  
1981 ◽  
Vol 134 (1) ◽  
pp. 15-19 ◽  
Author(s):  
B. Rutti ◽  
M. Keller ◽  
W. Ortiz ◽  
E. Stutz

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