ISSN: 0973-7510

E-ISSN: 2581-690X

Hari Ram, Lebin Thomas, Alok Kumar and Ved Pal Singh
1Applied Microbiology and Biotechnology Laboratory, Department of Botany,
University of Delhi, Delhi-110 007, India.
J Pure Appl Microbiol. 2014;8(3):2425-2431
© The Author(s). 2014
Received: 11/09/2013 | Accepted: 12/11/2013 | Published: 31/06/2014
Abstract

In nature, prolonged cell survival is governed by the accurate transmission of DNA material from one generation to the next. Accuracy of the transmission is achieved by the concerted action of several enzymes and proteins of DNA replication and DNA repair mechanisms. In both prokaryotes and eukaryotes, various enzymes contribute to the fidelity of replication. Bacteria contain five DNA polymerase enzymes (I, II, III, IV and V) which show active contribution in the fidelity of DNA replication. DNA polymerase I is the first identified DNA polymerase from Escherichia coli which is involved in the DNA replication by Okazaki fragment processing and nucleotide excision repair. DNA polymerase III is the main chromosomal replicative polymerase with high processivity and fidelity. DNA polymerase II, IV and V are SOS regulon regulated DNA repair enzymes, which are induced in response to DNA damage.

Keywords

Processivity, Fidelity, Trans-lesion synthesis (TLS)

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