Purification and properties of nuclease SP. 1991

J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
Department of Biochemistry, School of Medicine, Emory University, Atlanta, Georgia 30322.

Single-strand-specific nucleases are a diverse and important group of enzymes that are able to cleave a variety of DNA structures present in duplex molecules. Nuclease SP, an enzyme from spinach, has been purified to apparent homogeneity, allowing for the unambiguous characterization of a number of its physical properties as well as its DNA strand cleavage specificities. The effects of ionic strength, pH, divalent metal cations, and temperature on nuclease SP activity have been examined in detail. Nuclease SP was found to be quite thermostable and could be stimulated by Co2+. In addition, the cleavage of UV-damaged and undamaged supercoiled plasmid substrates under a variety of conditions suggests that at least two types of structures are recognized and processed by nuclease SP: UV photoproduct-induced distortions and unwound "nuclease hypersensitive sites". These studies indicate that nuclease SP is functionally related to other single-strand-specific nucleases and is a potential enzymatic tool for probing and manipulating various types of DNA structures.

UI MeSH Term Description Entries
D008670 Metals Electropositive chemical elements characterized by ductility, malleability, luster, and conductance of heat and electricity. They can replace the hydrogen of an acid and form bases with hydroxyl radicals. (Grant & Hackh's Chemical Dictionary, 5th ed) Metal
D009711 Nucleotides The monomeric units from which DNA or RNA polymers are constructed. They consist of a purine or pyrimidine base, a pentose sugar, and a phosphate group. (From King & Stansfield, A Dictionary of Genetics, 4th ed) Nucleotide
D010940 Plant Proteins Proteins found in plants (flowers, herbs, shrubs, trees, etc.). The concept does not include proteins found in vegetables for which PLANT PROTEINS, DIETARY is available. Plant Protein,Protein, Plant,Proteins, Plant
D004591 Electrophoresis, Polyacrylamide Gel Electrophoresis in which a polyacrylamide gel is used as the diffusion medium. Polyacrylamide Gel Electrophoresis,SDS-PAGE,Sodium Dodecyl Sulfate-PAGE,Gel Electrophoresis, Polyacrylamide,SDS PAGE,Sodium Dodecyl Sulfate PAGE,Sodium Dodecyl Sulfate-PAGEs
D004720 Endonucleases Enzymes that catalyze the hydrolysis of the internal bonds and thereby the formation of polynucleotides or oligonucleotides from ribo- or deoxyribonucleotide chains. EC 3.1.-. Endonuclease
D004795 Enzyme Stability The extent to which an enzyme retains its structural conformation or its activity when subjected to storage, isolation, and purification or various other physical or chemical manipulations, including proteolytic enzymes and heat. Enzyme Stabilities,Stabilities, Enzyme,Stability, Enzyme
D006863 Hydrogen-Ion Concentration The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH pH,Concentration, Hydrogen-Ion,Concentrations, Hydrogen-Ion,Hydrogen Ion Concentration,Hydrogen-Ion Concentrations
D006868 Hydrolysis The process of cleaving a chemical compound by the addition of a molecule of water.
D012492 Salts Substances produced from the reaction between acids and bases; compounds consisting of a metal (positive) and nonmetal (negative) radical. (Grant & Hackh's Chemical Dictionary, 5th ed) Salt
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships

Related Publications

J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
October 1976, Canadian journal of microbiology,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
November 1961, The Journal of biological chemistry,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
January 1980, Methods in enzymology,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
January 1980, Methods in enzymology,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
January 1973, National Institute of Animal Health quarterly,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
May 1971, The Journal of biological chemistry,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
October 1999, Journal of bacteriology,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
March 1984, The Journal of biological chemistry,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
November 2012, Sheng wu gong cheng xue bao = Chinese journal of biotechnology,
J A Strickland, and L G Marzilli, and J M Puckett, and P W Doetsch
July 1966, The Journal of biological chemistry,
Copied contents to your clipboard!