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A rapid procedure for isolating chromosomal DNA from Lactobacillus species and other Gram‐positive bacteria
Author(s) -
Ulrich R.L.,
Hughes T.A.
Publication year - 2001
Publication title -
letters in applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.698
H-Index - 110
eISSN - 1472-765X
pISSN - 0266-8254
DOI - 10.1111/j.1472-765x.2001.00866.x
Subject(s) - biology , microbiology and biotechnology , bacillus pumilus , subcloning , bacteria , ribotyping , genomic dna , enterococcus faecalis , polymerase chain reaction , lactobacillus acidophilus , propionibacterium , lactobacillus casei , dna , plasmid , genetics , staphylococcus aureus , probiotic , gene
R.L. ULRICH AND T.A. HUGHES. 2001 . This study describes a rapid procedure for the isolation of genomic DNA from various Gram‐positive bacteria. Species tested included Lactobacillus delbrueckii subsp. lactis ATCC 4797, Lact. acidophilus N2, Staphylococcus aureus, Staph. epidermidis, Propionibacterium jensenii P126 , Bacillus pumilus and Enterococcus faecalis . Our technique for chromosomal DNA isolation circumvents the need for phenol–chloroform extractions and caesium chloride gradients. Isolated DNA is consistently greater than 25 kb in size and can be used directly for subcloning, polymerase chain reaction amplification, restriction digestions and library construction.