Genome sequence of Brevibacillus laterosporus LMG 15441, a pathogen of invertebrates

Journal of Bacteriology

Volumn 193, Issue 19, 2011, Pages 5535-5536

  Djukic, Marvin ^a   Poehlein, Anja ^a   Thürmer, Andrea ^a   Daniel, Rolf ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL TOXIN; PEPTIDE DERIVATIVE; POLYKETIDE;

BACTERIAL CHROMOSOME; BACTERIAL GENOME; BREVIBACILLUS; BREVIBACILLUS LATEROSPORUS; DNA SEQUENCE; GENE SEQUENCE; INVERTEBRATE; NONHUMAN; NOTE; NUCLEOTIDE SEQUENCE; PLASMID; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ANIMALS; BREVIBACILLUS; GENOME, BACTERIAL; INVERTEBRATES; MOLECULAR SEQUENCE DATA;

BACTERIA (MICROORGANISMS); BREVIBACILLUS LATEROSPORUS; INVERTEBRATA;

EID: 80053604552     PISSN: 00219193     EISSN: 10985530     Source Type: Journal    
DOI: 10.1128/JB.05696-11     Document Type: Note

References (14)

1. Barsby, T., M. T. Kelly, and R. J. Andersen. 2002. Tupuseleiamides and basiliskamides, new acyldipeptides and antifungal polyketides produced in culture by a Bacillus laterosporus isolate obtained from a tropical marine habitat. J. Nat. Prod. 65:1447-1451.
2. Barth, H., K. Aktories, M. R. Popoff, and B. G. Stiles. 2004. Binary bacterial toxins: biochemistry, biology, and applications of common Clostridium and Bacillus proteins. Microbiol. Mol. Biol. Rev. 68:373-402.
3. Chung, M. C., et al. 2006. Secreted neutral metalloproteases of Bacillus anthracis as candidate pathogenic factors. J. Biol. Chem. 281:31408-31418.
4. de Oliveira, E. J., L. Rabinovitch, R. G. Monnerat, L. K. J. Passos, and V. Zahner. 2004. Molecular characterization of Brevibacillus laterosporus and its potential use in biological control. Appl. Environ. Microbiol. 70:6657-6664.
5. Desjardine, K., et al. 2007. Tauramamide, a lipopeptide antibiotic produced in culture by Brevibacillus laterosporus isolated from a marine habitat: structure elucidation and synthesis. J. Nat. Prod. 70:1850-1853.
6. Forsgren, E. 2010. European foulbrood in honey bees. J. Invertebr. Pathol. 103:S5-S9.
7. Geoffroy, C., J. Mengaud, J. E. Alouf, and P. Cossart. 1990. Alveolysin, the thiol-activated toxin of Bacillus alvei, is homologous to listeriolysin O, perfringolysin O, pneumolysin, and streptolysin O and contains a single cysteine. J. Bacteriol. 172:7301-7305.
8. Gerard, J., P. Haden, M. T. Kelly, and R. J. Andersen. 1996. Loloatin B, a cyclic decapeptide antibiotic produced in culture by a tropical marine bacterium. Tetrahedron Lett. 37:7201-7204.
9. Gerard, J. M., P. Haden, M. T. Kelly, and R. J. Andersen. 1999. Loloatins A-D, cyclic decapeptide antibiotics produced in culture by a tropical marine bacterium. J. Nat. Prod. 62:80-85.
10. Huang, X. W., et al. 2005. An extracellular protease from Brevibacillus laterosporus G4 without parasporal crystals can serve as a pathogenic factor in infection of nematodes. Res. Microbiol. 156:719-727.
11. Kuwajima, G., J. I. Asaka, T. Fujiwara, K. Node, and E. Kondo. 1986. Nucleotide sequence of the hag gene encoding flagellin of Escherichia coli. J. Bacteriol. 168:1479-1483.
12. Laubach, C. A. 1916. Studies on aerobic spore-bearing non-pathogenic bacteria. Spore-bearing organisms in water. J. Bacteriol. 1:505-512.
13. Samakovlis, C., B. Asling, H. G. Boman, E. Gateff, and D. Hultmark. 1992. In vitro induction of cecropin genes-an immune response in a Drosophila blood cell line. Biochem. Biophys. Res. Commun. 188:1169-1175.
14. Shida, O., H. Takagi, K. Kadowaki, and K. Komagata. 1996. Proposal for two new genera, Brevibacillus gen nov and Aneurinibacillus gen nov. Int. J. Syst. Bacteriol. 46:939-946.