High molecular weight deoxyribonucleic acid polymerase from crown gall tumor cells of periwinkle (Vinca rosea)

Biochemistry ◽  
1976 ◽  
Vol 15 (3) ◽  
pp. 688-697 ◽  
Author(s):  
John M. Gardner ◽  
Clarence I. Kado
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Tumor Cells ◽  
Crown Gall ◽  
Deoxyribonucleic Acid ◽  
Crown Gall Tumor ◽  
Vinca Rosea

Uptake of potassium ions by normal and crown-gall-tumor cells of Vinca rosea grown in tissue culture

Planta ◽  
1979 ◽  
Vol 146 (2) ◽  
pp. 113-117 ◽  
Author(s):  
Constance Bouricius Lentz ◽  
Thomas K. Hodges ◽  
Ann G. Matthysse
Keyword(s):  
Tissue Culture ◽  
Tumor Cells ◽  
Crown Gall ◽  
Potassium Ions ◽  
Crown Gall Tumor ◽  
Vinca Rosea

scholarly journals The photocarcinogenicity of anthracence: photochemical binding to deoxyribonucleic acid in tissue culture

1975 ◽  
Vol 149 (1) ◽  
pp. 289-291 ◽  
Author(s):  
G M Blackburn ◽  
P E Taussig
Keyword(s):  
Molecular Weight ◽  
Tissue Culture ◽  
High Molecular Weight ◽  
Deoxyribonucleic Acid ◽  
Radiation Doses ◽  
Mammalian Tissue ◽  
Hydrocarbon Molecule ◽  
High Radiation ◽  
High Molecular Weight Dna ◽  
Low Radiation Doses

Anthracene becomes covalently bound to high-molecular-weight DNA in mammalian tissue culture as a result of irradiation at 365 nm after the incubation of cells with the hydrocarbon. At high radiation doses, the extent of binding exceeds one hydrocarbon molecule per 103 bases, and is lethal. At low radiation doses, much decreased binding is observed, but a majority of cells remain viable and can be recultured.

N6-(Δ2-isopentenyl)adenosine from crown gall tumor tissue of Vinca rosea

1976 ◽  
Vol 15 (10) ◽  
pp. 1565 ◽  
Author(s):  
Chong-Maw Chen ◽  
Richard L. Eckert ◽  
James D. McChesney
Keyword(s):  
Crown Gall ◽  
Tumor Tissue ◽  
Crown Gall Tumor ◽  
Vinca Rosea ◽  
Isopentenyl Adenosine

scholarly journals Studies on the recovery of crown gall tumor cells

1976 ◽  
Vol 73 (10) ◽  
pp. 3562-3564 ◽  
Author(s):  
R. Turgeon ◽  
H. N. Wood ◽  
A. C. Braun
Keyword(s):  
Tumor Cells ◽  
Crown Gall ◽  
Crown Gall Tumor

Further Studies on the Mammalian High-Molecular-Weight Deoxyribonucleic Acid Polymerase Fraction

1974 ◽  
Vol 2 (5) ◽  
pp. 864-865 ◽  
Author(s):  
ANDREW M. HOLMES ◽  
IAN P. HESSLEWOOD ◽  
WILLIAM F. WAKELING ◽  
IRVING R. JOHNSTON
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Deoxyribonucleic Acid

scholarly journals Chromatography of transforming deoxyribonucleic acid on methylated albumin and by gel filtration

1974 ◽  
Vol 137 (3) ◽  
pp. 543-546
Author(s):  
G. R. Barker ◽  
P. Hodges
Keyword(s):  
Molecular Weight ◽  
Bacillus Subtilis ◽  
High Molecular Weight ◽  
Deoxyribonucleic Acid ◽  
Degradation Products ◽  
Gel Filtration ◽  
Agarose Gel ◽  
Transforming Activity ◽  
Different Strains ◽  
Two Peaks

1. Native DNA from two strains of Bacillus subtilis was chromatographed by stepwise elution from MAK (methylated albumin on kieselguhr). 2. Transforming activity was confined to two out of the three main fractions, activity being distributed between the two peaks differently for DNA from the different strains. 3. Fractionation of DNA from both strains on 2% agarose gel gave two components. Approx. 75% of the material was eluted within the void volume of the column. Approx. 25% of the material consisted of degradation products of lower molecular weight. 4. Chromatography on MAK of the material of high molecular weight eluted from agarose gel gave a number of peaks differing in molecular weight, indicating that degradation of the DNA takes place during chromatography on MAK. 5. The distribution of transforming activity among the fractions from MAK suggests that degradation occurs preferentially in certain regions of the DNA.

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