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Complete genome sequence of the industrial bacterium Bacillus licheniformis and comparisons with closely related Bacillus species

Michael W Rey1 email, Preethi Ramaiya1 email, Beth A Nelson1 email, Shari D Brody-Karpin1 email, Elizabeth J Zaretsky1 email, Maria Tang1 email, Alfredo Lopez de Leon1 email, Henry Xiang1 email, Veronica Gusti1 email, Ib Groth Clausen2,4 email, Peter B Olsen2 email, Michael D Rasmussen2 email, Jens T Andersen2 email, Per L Jørgensen2 email, Thomas S Larsen2 email, Alexei Sorokin3 email, Alexander Bolotin3 email, Alla Lapidus3,5 email, Nathalie Galleron3 email, S Dusko Ehrlich3 email and Randy M Berka1 email

Novozymes Biotech Inc, 1445 Drew Ave, Davis, CA 95616, USA

Novozymes A/S, Bagsværd, DK-2880, Denmark

Institut National de la Recherche Agronomique, Paris Cedex 75007, France

AstraZeneca International, Lund SE221 87, Sweden

Joint Genome Institute, Walnut Creek, CA 94598, USA

author email corresponding author email

Genome Biology 2004, 5:r77doi:10.1186/gb-2004-5-10-r77

Published: 13 September 2004

Subject areas: Microbiology and parasitology, Genome studies, Genetics, Biochemistry and structural biology

Abstract

Background

Bacillus licheniformis is a Gram-positive, spore-forming soil bacterium that is used in the biotechnology industry to manufacture enzymes, antibiotics, biochemicals and consumer products. This species is closely related to the well studied model organism Bacillus subtilis, and produces an assortment of extracellular enzymes that may contribute to nutrient cycling in nature.

Results

We determined the complete nucleotide sequence of the B. licheniformis ATCC 14580 genome which comprises a circular chromosome of 4,222,336 base-pairs (bp) containing 4,208 predicted protein-coding genes with an average size of 873 bp, seven rRNA operons, and 72 tRNA genes. The B. licheniformis chromosome contains large regions that are colinear with the genomes of B. subtilis and Bacillus halodurans, and approximately 80% of the predicted B. licheniformis coding sequences have B. subtilis orthologs.

Conclusions

Despite the unmistakable organizational similarities between the B. licheniformis and B. subtilis genomes, there are notable differences in the numbers and locations of prophages, transposable elements and a number of extracellular enzymes and secondary metabolic pathway operons that distinguish these species. Differences include a region of more than 80 kilobases (kb) that comprises a cluster of polyketide synthase genes and a second operon of 38 kb encoding plipastatin synthase enzymes that are absent in the B. licheniformis genome. The availability of a completed genome sequence for B. licheniformis should facilitate the design and construction of improved industrial strains and allow for comparative genomics and evolutionary studies within this group of Bacillaceae.


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