Nukacin 3299, a lantibiotic produced by Staphylococcus simulans 3299 identical to nukacin ISK-1

Veterinary Microbiology

Volumn 146, Issue 1-2, 2010, Pages 124-131

  Ceotto, Hilana ^a   Holo, Helge ^b   da Costa, Karlla Fernanda Silva ^a   Nascimento, Janaína dos Santos ^a   Salehian, Zhian ^b   Nes, Ingolf F ^b   Bastos, Maria do Carmo de Freire ^a  

^a FEDERAL UNIVERSITY OF RIO DE JANEIRO   (Brazil)

^b NORWEGIAN UNIVERSITY OF LIFE SCIENCES   (Norway)

Author keywords

Antimicrobial peptide; Bacteriocin; Bovine mastitis; Nukacin 3299; Staphylococcus simulans

Indexed keywords

BACTERIOCIN; LANTIBIOTIC; NUKACIN 3299; NUKACIN ISK 1; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANTIMICROBIAL ACTIVITY; ARTICLE; BACTERIAL GENE; DNA SEQUENCE; GENE CLUSTER; MASTITIS; NUCLEOTIDE SEQUENCE; NUKA GENE; ORF1 GENE; POLYMERASE CHAIN REACTION; PROTEIN SYNTHESIS; STAPHYLOCOCCUS SIMULANS;

BOVINAE; STAPHYLOCOCCUS SIMULANS; STAPHYLOCOCCUS WARNERI;

EID: 78049243918     PISSN: 03781135     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetmic.2010.04.032     Document Type: Article

References (24)

1. Aso Y., Nagao J., Koga H., Okuda K., Kanemasa Y., Sashihara T., Nakayama J., Sonomoto K. Heterologous expression and functional analysis of the gene cluster for the biosynthesis of and immunity to the lantibiotic, nukacin ISK-1. J. Biosci. Bioeng. 2004, 98:429-436.
2. Aso Y., Koga H., Sashihara T., Nagao J., Kanemasa Y., Nakayama J., Sonomoto K. Description of complete DNA sequence of two plasmids from the nukacin ISK-1 producer, Staphylococcus warneri ISK-1. Plasmid 2005, 53:164-178.
3. Bastos M.C.F., Ceotto H., Coelho M.L.V., Nascimento J.S. Staphylococcal antimicrobial peptides: relevant properties and potential biotechnological applications. Curr. Pharm. Biotechnol. 2009, 10:38-61.
4. Bierbaum G., Sahl H.-G. Lantibiotics: mode of action, biosynthesis and bioengineering. Curr. Pharm. Biotechnol. 2009, 10:2-18.
5. Brede D.A., Faye T., Johnsborg O., Odegård I., Nes I.F., Holo H. Molecular and genetic characterization of propionicin F, a bacteriocin from Propionibacterium freudenreichii. Appl. Environ. Microbiol. 2004, 70:7303-7310.
6. Call D.R., Davis M.A., Sawant A.A. Antimicrobial resistance in beef and dairy cattle production. Anim. Health Res. Rev. 2008, 9:159-167.
7. Campbell E.A., Westblade L.F., Darst S.A. Regulation of bacterial RNA polymerase sigma factor activity: a structural perspective. Curr. Opin. Microbiol. 2008, 11:121-127.
8. Ceotto H., Nascimento J.S., Brito M.A.V.P., Bastos M.C.F. Bacteriocin production by Staphylococcus aureus involved in bovine mastitis in Brazil. Res. Microbiol. 2009, 160:592-599.
9. Chandler M., Mahillon J. Insertion sequences revisited. Mobile DNA II 2002, 305-366. ASM Press, Washington. N.L. Craig, R. Craigie, M. Gellert, A.M. Lambowitz (Eds.).
10. Coelho M.L.V., Nascimento J.S., Fagundes P.C., Madureira D.J., Oliveira S.S., Brito M.A.V.P., Bastos M.C.F. Activity of staphylococcal bacteriocins against Staphylococcus aureus and Streptococcus agalactiae involved in bovine mastitis. Res. Microbiol. 2007, 158:625-630.
11. Cotter P.D., Hill C., Ross R.P. Bacteriocins: developing innate immunity for food. Nat. Rev. Microbiol. 2005, 3:777-788.
12. Dufour A., Hindré T., Haras D., Le Pennec J.-P. The biology of lantibiotics from the lacticin 481group is coming of age. FEMS Microbiol. Rev. 2007, 31:134-167.
13. Gálvez A., Abriouel H., Lopez R.L., Omar N.B. Bacteriocin-based strategies for food preservation. Int. J. Food Microbiol. 2007, 120:51-70.
14. Kimura H., Nagano R., Matsusaki H., Sonomoto K., Ishizaki A. A bacteriocin of strain Pediococcus sp. ISK-1 isolated from nukadoko, bed of fermented rice bran. Biosci. Biotechnol. Biochem. 1997, 61:1049-1051.
15. Minamikawa M., Inoue K.N., Yamazaki K. Purification and characterization of warnericin RB4, anti-Alicyclobacillus bacteriocin, produced by Staphylococcus warneri RB4. Curr. Microbiol. 2005, 51:22-26.
16. Nascimento J.S., Santos K.R.N., Gentilini E., Sordelli D., Bastos M.C.F. Phenotypic and genetic characterization of bacteriocin-producing strains of Staphylococcus aureus involved in bovine mastitis. Vet. Microbiol. 2002, 85:133-144.
17. Nascimento J.S., Fagundes P.C., Brito M.A.V.P., Bastos M.C.F. Production of bacteriocins by coagulase-negative staphylococci involved in bovine mastitis. Vet. Microbiol. 2005, 106:61-71.
18. Potter A., Ceotto H., Giambiagi-deMarval M., Santos K.R.N., Nes I.F., Bastos M.C.F. The gene bap, involved in biofilm production, is present in Staphylococcus spp. strains from nosocomial infections. J. Microbiol. 2009, 47:319-326.
19. Sambrook J., Fritsch E.F., Maniaris T. Molecular Cloning: A Laboratory Manual 1989, Cold Spring Harbor Laboratory, Cold Spring Harbor, pp. 3.6-3.34. 2nd edn.
20. Sashihara T., Kimura H., Higuchi T., Adachi A., Matsusaki H., Sonomoto K., Ishizaki A. A novel lantibiotic, nukacin ISK-1, of Staphylococcus warneri ISK-1: cloning of the structural gene and identification of the structure. Biosci. Biotechnol. Biochem. 2000, 64:2420-2428.
21. Schmitt-van de Leemput E., Zadoks R.N. Genotypic and phenotypic detection of macrolide and lincosamide resistance in Streptococcus uberis. J. Dairy Sci. 2007, 90:5089-5096.
22. Tuchscherr L.P.N., Gomez M.I., Buzzola F.R., Calvinho L.F., Lee J.C., Sordelli D.O. Characterization of a new variant of IS257 that has displaced the capsule genes within bovine isolates of Staphylococcus aureus. Infect. Immun. 2007, 75:5483-5488.
23. Wilaipun P., Zendo T., Okuda K., Nakayama J., Sonomoto K. Identification of the nukacin KQU-131, a new type-A (II) lantibiotic produced by Staphylococcus hominis KQU-131 isolated from Thai fermented fish product (Pla-Ra). Biosci. Biotechnol. Biochem. 2008, 72:2232-2235.
24. Zhao X., Lacasse P. Mammary tissue damage during bovine mastitis: causes and control. J. Anim. Sci. 2008, 86(13, Suppl. 1):57-65.