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RecBCD enzyme: mechanistic insights from mutants of a complex helicase-nuclease.

Authors :
Amundsen SK
Smith GR
Source :
Microbiology and molecular biology reviews : MMBR [Microbiol Mol Biol Rev] 2023 Dec 20; Vol. 87 (4), pp. e0004123. Date of Electronic Publication: 2023 Dec 04.
Publication Year :
2023

Abstract

SUMMARYRecBCD enzyme is a multi-functional protein that initiates the major pathway of homologous genetic recombination and DNA double-strand break repair in Escherichia coli . It is also required for high cell viability and aids proper DNA replication. This 330-kDa, three-subunit enzyme is one of the fastest, most processive helicases known and contains a potent nuclease controlled by Chi sites, hotspots of recombination, in DNA. RecBCD undergoes major changes in activity and conformation when, during DNA unwinding, it encounters Chi (5'-GCTGGTGG-3') and nicks DNA nearby. Here, we discuss the multitude of mutations in each subunit that affect one or another activity of RecBCD and its control by Chi. These mutants have given deep insights into how the multiple activities of this complex enzyme are coordinated and how it acts in living cells. Similar studies could help reveal how other complex enzymes are controlled by inter-subunit interactions and conformational changes.<br />Competing Interests: The authors declare no conflict of interest.

Details

Language :
English
ISSN :
1098-5557
Volume :
87
Issue :
4
Database :
MEDLINE
Journal :
Microbiology and molecular biology reviews : MMBR
Publication Type :
Academic Journal
Accession number :
38047637
Full Text :
https://doi.org/10.1128/mmbr.00041-23