Two temperature-sensitive mutations in the DNA binding subunit of EcoKI with differing properties
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
10612739
DOI
10.1111/j.1574-6968.2000.tb08881.x
PII: S0378-1097(99)00576-5
Knihovny.cz E-zdroje
- MeSH
- adenosintrifosfatasy metabolismus MeSH
- bakteriální proteiny genetika metabolismus MeSH
- bodová mutace * MeSH
- DNA bakterií metabolismus MeSH
- DNA restrikčně-modifikační enzymy genetika metabolismus MeSH
- Escherichia coli genetika metabolismus MeSH
- metylace DNA MeSH
- plazmidy genetika MeSH
- restrikční enzymy genetika metabolismus MeSH
- teplota MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adenosintrifosfatasy MeSH
- bakteriální proteiny MeSH
- DNA bakterií MeSH
- DNA restrikčně-modifikační enzymy MeSH
- endodeoxyribonuclease EcoKI MeSH Prohlížeč
- HSDS protein, Bacteria MeSH Prohlížeč
- restrikční enzymy MeSH
Two temperature-sensitive mutations in the hsdS gene, which encodes the DNA specificity subunit of the type IA restriction-modification system EcoKI, designated Sts1 (Ser(340)Phe) and Sts2 (Ala(204)Thr) had a different impact on restriction-modification functions in vitro and in vivo. The enzyme activities of the Sts1 mutant were temperature-sensitive in vitro and were reduced even at 30 degrees C (permissive temperature). Gel retardation assays revealed that the Sts1 mutant had significantly decreased DNA binding, which was temperature-sensitive. In contrast the Sts2 mutant did not show differences from the wild-type enzyme even at 42 degrees C. Unlike the HsdSts1 subunit, the HsdSts2 subunit was not able to compete with the wild-type subunit in assembly of the restriction enzyme in vivo, suggesting that the Sts2 mutation affects subunit assembly. Thus, it appears that these two mutations map two important regions in HsdS subunit responsible for DNA-protein and protein-protein interactions, respectively.
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General and molecular microbiology and microbial genetics in the IM CAS