Special Feature

User Panel

My Panel

My Panel

Bookmark Science Articles

Recent News
Bookmark / Share This Science Site

Rapid isolation of fungal genomic DNA suitable for long distance PCR.

Rapid isolation of fungal genomic DNA suitable for long distance PCR. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

  • Abstract Text of This Paper
  • Journal Published
  • MeSH Keywords of This Abstract
  • Chemicals and Substances Used in this Paper
  • Grants and Granting Agency of this Research
  • Database Accession Numbers Used in this Paper
  • Related Papers
  • Related Research Tags
  • Rate this Research Paper
  • Rapid isolation of fungal genomic DNA suitable for long distance PCR. Abstract Text:

    s l de maeseneireS L De Maeseneire,i n van bogaertI N Van Bogaert,t dauvrinT Dauvrin,w k soetaertW K Soetaert,e j vandammeE J Vandamme,s l de maeseneireS L De Maeseneire,i n van bogaertI N Van Bogaert,t dauvrinT Dauvrin,w k soetaertW K Soetaert,e j vandammeE J Vandamme,s l de maeseneireS L De Maeseneire,i n van bogaertI N Van Bogaert,t dauvrinT Dauvrin,w k soetaertW K Soetaert,e j vandammeE J Vandamme,

    A quick and reliable method for screening fungal transformants for specific genetic modifications is essential for many molecular applications. We have compared the applicability of a few rapid DNA extraction methods for Myrothecium and Aspergillus and tested the resulting DNA as to its suitability for PCR. For Myrothecium gramineum, the highest DNA concentration was obtained with the procedure described by N. Vanittanakom et al. (J Clin Microbiol 2002, 40: 1739-1742). For A. nidulans, concentrations higher than 100 ng/mul were reached with the glass bead, the LiCl, the boiling, the liquid N(2) and the protoplast-based method. Samples of M. gramineum resulting from the boiling and the liquid N(2) procedure were suitable for the amplification of fragments up to 2.3 kb. The direct use of mycelium from M. gramineum in the PCR tube can be employed for the reproducible amplification of fragments up to 1 kb. Amplification of fragments up to 4.3 kb requires the use of the Elongase Mix on samples extracted with the liquid N(2) procedure.

    Rapid isolation of fungal genomic DNA suitable for long distance PCR. Publishing Authors By Initials

    sl de maeseneireSL De Maeseneire,in van bogaertIN Van Bogaert,t dauvrinT Dauvrin,wk soetaertWK Soetaert,ej vandammeEJ Vandamme,sl de maeseneireSL De Maeseneire,in van bogaertIN Van Bogaert,t dauvrinT Dauvrin,wk soetaertWK Soetaert,ej vandammeEJ Vandamme,sl de maeseneireSL De Maeseneire,in van bogaertIN Van Bogaert,t dauvrinT Dauvrin,wk soetaertWK Soetaert,ej vandammeEJ Vandamme,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Rapid isolation of fungal genomic DNA suitable for long distance PCR. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Biotechnology letters

    VOLUME: 29

    Page Numbers: 1845-55

    Journal Abbreviation: Biotechnol. Lett.

    ISSN: 0141-5492

    DAY: 7

    MONTH: 08

    YEAR: 2007

    Rapid isolation of fungal genomic DNA suitable for long distance PCR. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8008051

    Rapid isolation of fungal genomic DNA suitable for long distance PCR. Keywords Mesh Terms:

    KEYWORDS:

    MESH TERMS:

    Chemical & Substance for Abstract: Rapid isolation of fungal genomic DNA suitable for long distance PCR. Information

    Substance Name:

    Registry Number:

    Grant and Affiliation Information for Rapid isolation of fungal genomic DNA suitable for long distance PCR.

    AFFILIATION: Laboratory of Industrial Microbiology and Biocatalysis, Department of Biochemical and Microbial Technology, Ghent University, Coupure links 653, Gent, 9000, Belgium, Sofie.DeMaeseneire@UGent.be.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: Biotechnol Lett

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    Rapid isolation of fungal genomic DNA suitable for long distance PCR Related Publications

     

    Molecular Station USER Menu

    Welcome to Molecular Station!

    You have to register before you can post on our forums or use our advanced features. Register Now! Its Free and Fast!

    Already registered? Login now below.

    User Name:

    Password:

    Already registered and Forgot your password? Click below to recover it.

    Recover Lost Password

    Join now - it's fast and free!

    Molecular Station is THE largest network of researchers, scientists and science lovers anywhere!

    Research Terms of Usage and Disclaimer
    Home
    Features

    Protocols

    DNA Forum

    Science Forum

    DNA Forum
    Biology Forum

    Science News


    [CaRP] XML error: Invalid document end at line 2

    For more click here:Science News