Thermolabile exonucleases
The invention provides an exonuclease or an enzymatically active fragment thereof, said exonuclease having the amino acid sequence of SEQ ID No. 1 or an amino acid sequence which is at least about 50% identical thereto, wherein said exonuclease or enzymatically active fragment thereof (i) is substantially irreversibly inactivated by heating at a temperature of about 55° C. for 10 minutes in a buffer consisting of 10 mM Tris-HCI, pH 8.5 at 25° C., 50 mM KCI and 5 mM MgCI 2 ; (ii) is substantially specific for single stranded DNA; and (iii) has a 3′-5′ exonuclease activity. The invention further provides a method of removing single stranded DNA from a sample, a method of nucleic acid amplification, a method of reverse transcription and a method of nucleic acid sequence analysis in which the exonuclease or enzymatically active fragment thereof is used. The invention still further provides nucleic acids encoding said exonuclease or an enzymatically active fragment thereof and kits or compositions comprising the same.
1. A method of removing single stranded DNA from a sample, said method comprising contacting the sample with an exonuclease or enzymatically active fragment thereof under conditions which permit the digestion of at least a portion of any single stranded DNA present in the sample and then heating the exonuclease treated sample to inactivate said exonuclease or enzymatically active fragment thereof, wherein said exonuclease has the amino acid sequence of SEQ ID NO:1 or an amino acid sequence which is at least about 85% identical thereto, wherein said enzymatically active fragment of said exonuclease is at least about 85% identical to the amino acid sequence of said exonuclease, wherein said exonuclease or enzymatically active fragment thereof
(i) is at least 90% irreversibly inactivated by heating at a temperature of about 55° C. for 10 mins in a buffer consisting of 10 mM Tris-HCl, pH 8.5 at 25° C., 50 mM KCl and 5 mM MgCl 2 ;
(ii) has activity against double stranded DNA that is equal to or less than 15% of its activity against an equivalent amount of single stranded DNA under the same assay conditions; and
(iii) has a 3′-5′ exonuclease activity.
2. A method of removing single stranded DNA from a sample, said method comprising contacting the sample with an exonuclease or enzymatically active fragment thereof under conditions which permit the digestion of at least a portion of any single stranded DNA present in the sample and then heating the exonuclease treated sample to inactivate said exonuclease or enzymatically active fragment thereof, wherein said exonuclease has an amino acid sequence selected from:
SEQ ID NO:1 or an amino acid sequence which is at least 85% identical thereto,
wherein said enzymatically active fragment of said exonuclease is at least about 85% identical to the amino acid sequence of said exonuclease,
wherein said exonuclease or enzymatically active fragment thereof
(i) is substantially at least 90% irreversibly inactivated by heating at a temperature of about 55° C. for 10 mins in a buffer consisting of 10 mM Tris-HCl, pH 8.5 at 25° C., 50 mM KCl and 5 mM MgCl 2 ;
(ii) is substantially specific for has activity against double stranded DNA that is equal to or less than 15% of its activity against an equivalent amount of single stranded DNA under the same assay conditions; and
(iii) has a 3′-5′ exonuclease activity.
3. The method as claimed in claim 1 , wherein said exonuclease has an amino acid sequence selected from any one of SEQ ID NO:1 and SEQ ID:11.
4. The method of claim 1 , wherein said sample is the product of a nucleic acid amplification reaction or the product of a reverse transcription reaction or a sample for sequence analysis.
5. The method of claim 4 , wherein said nucleic acid amplification reaction is selected from PCR, 3SR, SDA, LAR/LCR, and LAMP.
6. The method as claimed in claim 2 , wherein said exonuclease has an amino acid sequence selected from any one of SEQ ID NO:1 and SEQ ID NO:11.
7. The method of claim 2 , wherein said sample is the product of a nucleic acid amplification reaction or the product of a reverse transcription reaction or a sample for sequence analysis.
8. The method of claim 1 , wherein said sample is a sample of biological macromolecules.
9. The method of claim 1 , wherein said sample comprises a nucleic acid, a protein, a carbohydrate polymer or a lipid.
10. The method of claim 1 , wherein said sample comprises a double stranded nucleic acid, a DNA:RNA duplex of interest or a recombinantly produced protein.
11. The method of claim 2 , wherein said sample is a sample of biological macromolecules.
12. The method of claim 2 , wherein said sample comprises a nucleic acid, a protein, a carbohydrate polymer or a lipid.
13. The method of claim 6 , wherein said sample comprises a double stranded nucleic acid, a DNA:RNA duplex of interest or a recombinantly produced protein.
14. The method of claim 7 , wherein said nucleic acid amplification reaction is selected from PCR, 3SR, SDA, LAR/LCR, and LAMP.