Nucleic Acids Research, Vol 24, Issue 18 3590-3592, Copyright © 1996 by Oxford University Press
LE Sears, B Zhou, JM Aliotta, RD Morgan and H Kong
BcgI and BcgI-like restriction endonucleases have a very distinct
characteristic which causes them to differ from the other classified
restriction enzymes; they all cleave double-stranded DNA specifically on
both sides of the recognition sequence to excise a short DNA fragment
including the recognition sites. Here we report a new BcgI- like
restriction endonuclease, BaeI, isolated from Bacillus sphaericus. Like
BcgI, BaeI also cleaves double-stranded DNA on both strands upstream and
downstream of its recognition sequence (10/15)ACNNNNGTAYC(12/7). There are
two dominant polypeptides in the final preparation of BaeI with molecular
masses of approximately 80 and 55 kDa. Both are slightly larger than the
two BcgI subunits. BaeI requires both Mg2+ and AdoMet to cleave DNA.
Accompanying bilateral cleavage activity, the heteromeric BaeI also has an
N6-adenine methyltransferase activity which modifies the symmetrically
located adenines within its recognition sequence.
ARTICLES
BaeI, another unusual BcgI-like restriction endonuclease
New England Biolabs, Inc., Beverly, MA 01915, USA.
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