Method for nucleic acid sequencing
A technology of nucleic acid sequencing and nucleic acid sequence, which is applied in the direction of biochemical equipment and methods, microbial measurement/inspection, etc., can solve the problems of cumbersome steps and large consumption of reagents, reduce error messages, ensure accuracy, avoid mutations and wrong effect
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Embodiment 1
[0013] Example 1: Escherichia coli exonuclease III (exo III) was used to degrade phosphodiester bonds in double-stranded DNA molecules. Catalytic double-stranded DNA releases 5'-mononucleotides from the 3'-OH end in the direction of 3'→5', and then detects the released single nucleotides one by one to achieve sequencing.
Embodiment 2
[0014] Example 2: Using lambda bacteriophage exonuclease (λexo) to catalyze the degradation of double-stranded DNA molecules from the 5'-P end to carry out step-by-step hydrolysis to release 5'-mononucleotides, and then detect the released single nucleotides one by one Detection, enabling sequencing.
Embodiment 3
[0015] Example 3: Escherichia coli exonuclease I (exo I) was used to degrade single-stranded DNA molecules, and the cleavage products were identified and sequenced, thereby realizing the sequencing of the entire sequence.
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