Variant DNA polymerases having improved properties and method for improved isothermal amplification of a target DNA
Variants of the bacteriophage B103 DNA polymerase are described herein. The variant has improved properties, that include when compared to wild-type Phi29 DNA polymerase, at least one of the following: increased thermostability, improved reaction rate for DNA amplification, reduced background and a reduction of bias. Methods of using the DNA polymerase variant are also described herein.
1. A method, comprising:
combining with a target DNA, a DNA polymerase with an amino acid sequence that has at least 99% sequence identity with SEQ ID NO:5; and
amplifying the target DNA.
2. The method according to claim 1 , further comprising amplifying the target DNA in a high salt buffer.
3. The method according to claim 1 , further comprising amplifying the target DNA at a temperature in the range of 30° C.-42° C.
4. The method according to claim 3 , further comprising obtaining reduced sequence bias of the substrate DNA with the polymerase in claim 1 compared to the wild-type Phi29 DNA polymerase under the same reaction conditions.
5. The method according claim 3 , further comprising obtaining a higher rate of amplification compared to the rate of amplification using wild-type Phi29 DNA polymerase under the same reaction conditions.
6. The method according to claim 3 , further comprising obtaining an improved amplification yield after a reaction time of 2 hours compared to the yield obtained with wild-type Phi29 DNA polymerase under the same reaction conditions.
7. The method according to claim 1 , further comprising amplifying the target DNA in a high salt buffer.
8. A method, comprising:
combining with a target DNA, a DNA polymerase with an amino acid sequence that has at least 95% sequence identity with SEQ ID NO:2 and has at least one, two, three, four, five, six or seven amino acid substitutions at positions selected from the group consisting of: 147, 221, 318, 503, 511, 544 and 550; and
amplifying the target DNA.
9. The method of claim 8 , wherein the one to seven substitutions are selected from the group of substitutions consisting of: A147K, R221Y, A318G, A503M, I511V, R544K and T550K.
10. The method according to claim 8 , further comprising amplifying the target DNA at a temperature in the range of 30° C.-42° C.
11. The method according to claim 8 , further comprising obtaining an improved representation of the substrate DNA compared to the biased representation of wild-type Phi29 DNA polymerase under the same reaction conditions.
12. The method according claim 8 , further comprising obtaining a higher rate of amplification compared to the rate of amplification using wild-type Phi29 DNA polymerase under the same reaction conditions.
13. The method according to claim 8 , further comprising obtaining an improved yield of amplification after a reaction time of 2 hours compared to the yield obtained with wild-type Phi29 DNA polymerase under the same reaction conditions.