Abstract

Problem statement: Pyrosequencing has the potential to rapidly and reliably sequence DNA taking advantages over traditional Sanger di-deoxy sequencing approach. Approach: A comprehensive review of the literature on the principles, applications, challenges and prospects of pyrosequencing was performed. Results: Pyrosequencing was a DNA sequencing technology based on the sequencing-by-synthesis principle. It employs a series of four enzymes to accurately detect nucleic acid sequences during the synthesis. Pyrosequencing had the potential advantages of accuracy, flexibility, parallel processing and could be easily automated. The technique dispenses with the need for labeled primers, labeled nucleotides and gel-electrophoresis. Pyrosequencing had opened up new possibilities for performing sequence-based DNA analysis. The method had been proven highly suitable for single nucleotide polymorphism analysis and sequencing of short stretches of DNA. Pyrosequencing had been successful for both confirmatory sequencing and de novo sequencing. By increasing the read length to higher scores and by shortening the sequence reaction time per base calling, pyrosequencing may take over many broad areas of DNA sequencing applications as the trend was directed to analysis of fewer amounts of specimens and large-scale settings, with higher throughput and lower cost. Conclusion/Recommendations: The Competitiveness of pyrosequencing with other sequencing methods can be improved in future."

Highlights

  • Genome sequencing has provided us with powerful insights into the genetic make-up of the microbial world and has spearheaded a host of revolutionary technologies, such as microarrays and proteomics that have transformed the field of microbiological research

  • There are limitations in this method, which could be complemented with other techniques (Gharizadeh et al, 2007)

  • A schematic representation of pyrosequencing is luminometric detection of pyrophosphate that is released during primer-directed DNA polymerase catalyzed nucleotide incorporation

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Summary

INTRODUCTION

Genome sequencing has provided us with powerful insights into the genetic make-up of the microbial world and has spearheaded a host of revolutionary technologies, such as microarrays and proteomics that have transformed the field of microbiological research. Because the added nucleotide is known, the alternative to the conventional Sanger method for de sequence of the template can be determined A schematic representation of pyrosequencing is luminometric detection of pyrophosphate that is released during primer-directed DNA polymerase catalyzed nucleotide incorporation It is suited for DNA sequencing of up to one hundred bases and it offers a number of unique advantages (Gharizadeh, 2003). In Pyrosequencing (Nyren and Skarpnack, 2001) the sequencing primer is hybridized to a single-stranded DNA biotinlabeled template and mixed with the enzymes; DNA polymerase, ATP sulfurylase, luciferase and apyrase and the substrates adenosine 5’ phosphosulfate (Ronaghi, 2001). Pyrosequencing technology is relatively new and there lies ample room for versatile developments in both chemistry and instrumentation This technology is already time-and cost-competitive as compared to the most conventional sequencing methods. By efficiency at elevated temperatures and to run the reaction employing Sequenase (Gharizadeh et al, 2004), an in miniaturized formats (Ronaghi, 2001). exonuclease deficient T7 DNA polymerase, the poly-T homopolymer string reads were significantly improved by generation of significantly more synchronized

CONCLUSION
34. PMID: 15797362
Findings
26-28. PMID: 12545532
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