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Engineered DNA polymerase improves PCR results for plastid DNA(1)

• Premise of the study: Secondary metabolites often inhibit PCR and sequencing reactions in extractions from plant material, especially from silica-dried and herbarium material. A DNA polymerase that is tolerant to inhibitors improves PCR results. • Methods and Results: A novel DNA amplification sys...

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Detalles Bibliográficos
Autores principales: Schori, Melanie, Appel, Maryke, Kitko, AlexaRae, Showalter, Allan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Botanical Society of America 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105373/
https://www.ncbi.nlm.nih.gov/pubmed/25202519
http://dx.doi.org/10.3732/apps.1200519
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author Schori, Melanie
Appel, Maryke
Kitko, AlexaRae
Showalter, Allan M.
author_facet Schori, Melanie
Appel, Maryke
Kitko, AlexaRae
Showalter, Allan M.
author_sort Schori, Melanie
collection PubMed
description • Premise of the study: Secondary metabolites often inhibit PCR and sequencing reactions in extractions from plant material, especially from silica-dried and herbarium material. A DNA polymerase that is tolerant to inhibitors improves PCR results. • Methods and Results: A novel DNA amplification system, including a DNA polymerase engineered via directed evolution for improved tolerance to common plant-derived PCR inhibitors, was evaluated and PCR parameters optimized for three species. An additional 31 species were then tested with the engineered enzyme and optimized protocol, as well as with regular Taq polymerase. • Conclusions: PCR products and high-quality sequence data were obtained for 96% of samples for rbcL and 79% for matK, compared to 29% and 21% with regular Taq polymerase.
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spelling pubmed-41053732014-09-08 Engineered DNA polymerase improves PCR results for plastid DNA(1) Schori, Melanie Appel, Maryke Kitko, AlexaRae Showalter, Allan M. Appl Plant Sci Protocol Note • Premise of the study: Secondary metabolites often inhibit PCR and sequencing reactions in extractions from plant material, especially from silica-dried and herbarium material. A DNA polymerase that is tolerant to inhibitors improves PCR results. • Methods and Results: A novel DNA amplification system, including a DNA polymerase engineered via directed evolution for improved tolerance to common plant-derived PCR inhibitors, was evaluated and PCR parameters optimized for three species. An additional 31 species were then tested with the engineered enzyme and optimized protocol, as well as with regular Taq polymerase. • Conclusions: PCR products and high-quality sequence data were obtained for 96% of samples for rbcL and 79% for matK, compared to 29% and 21% with regular Taq polymerase. Botanical Society of America 2013-01-31 /pmc/articles/PMC4105373/ /pubmed/25202519 http://dx.doi.org/10.3732/apps.1200519 Text en © 2013 Botanical Society of America
spellingShingle Protocol Note
Schori, Melanie
Appel, Maryke
Kitko, AlexaRae
Showalter, Allan M.
Engineered DNA polymerase improves PCR results for plastid DNA(1)
title Engineered DNA polymerase improves PCR results for plastid DNA(1)
title_full Engineered DNA polymerase improves PCR results for plastid DNA(1)
title_fullStr Engineered DNA polymerase improves PCR results for plastid DNA(1)
title_full_unstemmed Engineered DNA polymerase improves PCR results for plastid DNA(1)
title_short Engineered DNA polymerase improves PCR results for plastid DNA(1)
title_sort engineered dna polymerase improves pcr results for plastid dna(1)
topic Protocol Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105373/
https://www.ncbi.nlm.nih.gov/pubmed/25202519
http://dx.doi.org/10.3732/apps.1200519
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