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Mitochondrial DNA polymerase, deoxyribonuclease and ribonuclease H activities from brain of chick embryo
Author(s) -
Luis Soriano,
J Smith,
Y Croisille,
B. Dastugue
Publication year - 1974
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/1.9.1085
Subject(s) - biology , dna polymerase , polymerase , ribonuclease , taq polymerase , deoxyribonuclease , dna , microbiology and biotechnology , rnase p , biochemistry , dna clamp , enzyme , polymerase chain reaction , reverse transcriptase , rna , thermus aquaticus , gene
R-DNA polymerase, D-DNA polymerase, DNase and RNase H activities in mitochondria from chick embryonic brain were studied by ion-exchange chromatography. Two main fractions were separated according to their chromatographic behaviour: a fraction M Ib which is eluted with the washing buffer from two successive DEAE-cellulose columns and a fraction M IV which is eluted at 400 mM KC1 from a phosphocellulose column. Although the two fractions contain both the DNA polymerase and the degrading activities, all the specific activities are higher in fraction M IV than in fraction M Ib. Heat inactivation experiments have shown that R-DNA polymerase is inactivated in both fractions, whereas RNase H and DNase are not affected. Thus, degrading activities and R-DNA polymerase activity seem to be catalyzed by different molecular entities. However the fact that in most cases these activities co-chromatograph suggests that the corresponding molecules form rather stable complexes.

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