Abstract
Hemophilus influenzae—transforming DNA, which has been inactivated by ultra-violet radiation, is reactivated by visible light in the presence of a cell-free extract of Escherichia coli B. The time rate of reactivation is increased by increasing the E. coli extract concentration, the temperature, and the intensity of illumination. Only DNA containing an ultraviolet-damaged genetic marker exhibits increased transforming activity after treatment with the photoreactivating system. The reactivating capacity of the extract remains in the top supernatant after centrifugation at 110,000 x g for 1 hour and is not present in the pellet. This capacity is destroyed by heating to 90°C. for 1 minute. The active system of the E. coli extract is separable into dialyzable, heat-stable and non-dialyzable, heat-labile fractions. The dialyzable fraction contains at least one component which limits the maximum degree of recovery attained.
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Selected References
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- ALEXANDER H. E., LEIDY G., HAHN E. Studies on the nature of hemophilus influenzae cells susceptible to heritable changes by desoxyribonucleic acids. J Exp Med. 1954 Jun 1;99(6):505–533. doi: 10.1084/jem.99.6.505. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Avery O. T., Macleod C. M., McCarty M. STUDIES ON THE CHEMICAL NATURE OF THE SUBSTANCE INDUCING TRANSFORMATION OF PNEUMOCOCCAL TYPES : INDUCTION OF TRANSFORMATION BY A DESOXYRIBONUCLEIC ACID FRACTION ISOLATED FROM PNEUMOCOCCUS TYPE III. J Exp Med. 1944 Feb 1;79(2):137–158. doi: 10.1084/jem.79.2.137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BLUM H. F., ROBINSON J. C., LOOS G. M. The loci of action of ultraviolet and x-radiation and of photorecovery in the egg and sperm of the sea urchin Arbacia punctulata. J Gen Physiol. 1951 Nov;35(2):323–342. doi: 10.1085/jgp.35.2.323. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BRANDT C. L., GIESE A. C. Photoreversal of nuclear and cytoplasmic effects of short ultraviolet radiation on Paramecium caudatum. J Gen Physiol. 1956 May 20;39(5):735–751. doi: 10.1085/jgp.39.5.735. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HERRIOTT R. M., BARLOW J. L. Preparation, purification, and properties of E. coli virus T2. J Gen Physiol. 1952 May;36(1):17–28. doi: 10.1085/jgp.36.1.17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KELNER A. Growth, respiration, and nucleic acid synthesis in ultraviolet-irradiated and in photoreactivated Escherichia coli. J Bacteriol. 1953 Mar;65(3):252–262. doi: 10.1128/jb.65.3.252-262.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kelner A. PHOTOREACTIVATION OF ULTRAVIOLET-IRRADIATED ESCHERICHIA COLI, WITH SPECIAL REFERENCE TO THE DOSE-REDUCTION PRINCIPLE AND TO ULTRAVIOLET-INDUCED MUTATION. J Bacteriol. 1949 Oct;58(4):511–522. doi: 10.1128/jb.58.4.511-522.1949. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LENNOX E. S., LURIA S. E., BENZER S. On the mechanism of photoreactivation of ultraviolet-inactivated bacteriophage. Biochim Biophys Acta. 1954 Dec;15(4):471–474. doi: 10.1016/0006-3002(54)90003-7. [DOI] [PubMed] [Google Scholar]
- NORTHROP J. H. The effect of ultraviolet and white light on growth rate, lysis, and phage production of Bacillus megatherium. J Gen Physiol. 1957 May 20;40(5):653–661. doi: 10.1085/jgp.40.5.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NOVICK A., SZILARD L. Experiments on light-reactivation of ultra-violet inactivated bacteria. Proc Natl Acad Sci U S A. 1949 Oct;35(10):591–600. doi: 10.1073/pnas.35.10.591. [DOI] [PMC free article] [PubMed] [Google Scholar]
- RAVIN A. W. A quantitative study of autogenic and allogenic transformations in Pneumococcus. Exp Cell Res. 1954 Aug;7(1):58–82. doi: 10.1016/0014-4827(54)90042-7. [DOI] [PubMed] [Google Scholar]
