Extracellularly secreted nuclease
The purpose of the present invention is to provide a nuclease that secretes natural nonpathogenic microorganisms extracellularly, has higher specific activity than conventional nucleases, and is useful in nucleolytic degradation on an industrial scale. This purpose is achieved with an extracellularly secreted nuclease derived from Streptomyces bacteria, the nuclease having specific activity equal to or greater than the specific activity of Benzonase® when supplied to double-stranded DNA for 30 minutes at 37° C. in 20 mM Tris/HCl (pH 8.5) containing 1 mM MgCl 2 and 1 mM CaCl 2 after purification, using double-stranded DNA, single-stranded DNA, and RNA as substrates.
1. A method of degrading nucleic acids comprising:
providing a sample comprising nucleic acids; and
contacting the sample with a purified nuclease under conditions sufficient to degrade the nucleic acids;
wherein the purified nuclease has the amino acid sequence of SEQ ID NO:1 or SEQ ID NO:2.
2. The method according to claim 1 , wherein the nucleic acids are DNA.
3. The method according to claim 1 , wherein the purified nuclease is purified from bacteria of the genus Streptomyces.
4. The method according to claim 1 , wherein substrates of the nuclease comprise double-stranded DNA, single-stranded DNA, and RNA.
5. The method according to claim 1 , wherein the nuclease has a specific activity that is at least 90% of the specific activity of BENZONASE (Registered Trademark) when the nuclease is purified, and
wherein the specific activity is measured by determining the specific activity of the purified nuclease and the specific activity of the BENZONASE (Registered Trademark) when subjected to double-stranded DNA for 30 minutes at 37 degrees Celsius in 20 mM of Tris/HCl at pH 8.5 that comprises 1 mM of MgCl 2 and 1 mM of CaCl 2 .
6. The method according to claim 1 , wherein the nuclease requires Mg 2+ or Mn 2+ as divalent metal ion.
7. The method according to claim 1 , wherein substrates of the nuclease comprise double-stranded DNA, single-stranded DNA, and RNA,
wherein the nuclease is purified from bacteria of the genus Streptomyces,
wherein the nuclease has a specific activity that is at least 90% of the specific activity of BENZONASE (Registered Trademark) when the nuclease is purified, and wherein the specific activity is measured by determining the specific activity of the purified nuclease and the specific activity of the BENZONASE (Registered Trademark) when subjected to double-stranded DNA for 30 minutes at 37 degrees Celsius in 20 mM of Tris/HCl at pH 8.5 that comprises 1 mM of MgCl 2 and 1 mM of CaCl 2 , and
wherein the nuclease requires Mg 2+ or Mn 2+ as divalent metal ion.
8. The method of claim 1 , wherein the purified nuclease of SEQ ID NO: 1 or SEQ ID NO: 2 is expressed from an expression vector comprising the nucleic acids that code for SEQ ID NO: 1 or SEQ ID NO: 2, wherein the nucleic acids that code for SEQ ID NO:1 or SEQ ID NO: 2 are operably linked to an expression control sequence, wherein the expression control sequence comprises a drug resistance gene.