Affiliation:
1. Present address: Argonne National Laboratory, Bioscience Division, Argonne, IL 60439.
2. Department of Biological Sciences, Northern Illinois University, DeKalb, Illinois 60115
3. Present address: Department of Surgery, K4/638 Comprehensive Cancer Center, University of Wisconsin—Madison, Madison, WI 53792.
Abstract
ABSTRACT
Bacillus
megaterium
QM B1551 plasmid pBM400, one of seven indigenous
plasmids, has been labeled with a selectable marker, isolated,
completely sequenced, and partially characterized. A sequence of 53,903
bp was generated, revealing a total of 50 predicted open reading frames
(ORFs); 33 were carried on one strand and 17 were carried on the other.
These ORFs comprised 57% of the pBM400 sequence. Besides the
replicon region and a complete rRNA operon that have previously been
described, several interesting genes were found, including genes for
predicted proteins for cell division (FtsZ and FtsK), DNA-RNA
interaction (FtsK, Int/Rec, and reverse transcriptase), germination
(CwlJ), styrene degradation (StyA), and heavy metal resistance (Cu-Cd
export and ATPase). Three of the ORF products had high similarities to
proteins from the
Bacillus anthracis
virulence plasmid pXO1.
An insertion element with similarity to the IS
256
family and
several hypothetical proteins similar to those from the chromosomes of
other
Bacillus
and
Lactococcus
species were present.
This study provides a basis for isolation and sequencing of other
high-molecular-weight plasmids from QM B1551 and for understanding the
role of megaplasmids in gram-positive bacteria. The genes carried by
pBM400 suggest a possible role of this plasmid in the survival of
B. megaterium
in hostile environments with heavy metals or
styrene and also suggest that there has been an exchange of genes
within the gram-positive bacteria, including
pathogens.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
19 articles.
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