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Literature summary for 3.1.30.1 extracted from

  • Pimkin, M.; Miller, C.G.; Blakesley, L.; Oleykowski, C.A.; Kodali, N.S.; Yeung, A.T.
    Characterization of a periplasmic S1-like nuclease coded by the Mesorhizobium loti symbiosis island (2006), Biochem. Biophys. Res. Commun., 343, 77-84.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
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Mesorhizobium loti

Inhibitors

Inhibitors Comment Organism Structure
1,10-phenanthroline 0.24 mM, complete inhibition of plasmid nicking activity Mesorhizobium loti
MgCl2 50 mM, 25% inhibition Mesorhizobium loti
NaCl 100 mM, 20% inhibition Mesorhizobium loti

Localization

Localization Comment Organism GeneOntology No. Textmining
periplasmic space
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Mesorhizobium loti 42597
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Metals/Ions

Metals/Ions Comment Organism Structure
NaCl maximal activity below 50 mM Mesorhizobium loti

Organism

Organism UniProt Comment Textmining
Mesorhizobium loti
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-
-

Purification (Commentary)

Purification (Comment) Organism
recombinant carboxy-terminal hexahistidine tag fusion protein Mesorhizobium loti

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
DNA + H2O at acidic pH the enzyme is 25times more active on single-stranded DNA than on double-stranded DNA and 3times more active on single-stranded DNA than on single-stranded RNA. At neutral pH the RNase activity exceeds the DNase activity. The enzyme nicks supercoiled RF-I plasmid DNA and rapidly cuts the phosphodiester bond across from the nick in the resultant relaxed RF-II plasmid DNA. Mesorhizobium loti 5'-phosphomononucleotides + 5'-phosphooligonucleotides
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Synonyms

Synonyms Comment Organism
M1 nuclease
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Mesorhizobium loti