2011
DOI: 10.1016/j.plasmid.2010.11.008
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Functional analysis and application of the cryptic plasmid pBSG3 harboring the RapQ–PhrQ system in Bacillus amyloliquefaciens B3

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Cited by 14 publications
(12 citation statements)
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“…A plasmid was evident from strain AP143. High coverage contigs from the assembled genome sequence of AP143 (data not shown) were screened by BLASTn and one of the contigs showed high identity (99%) with plasmid pBSG3 from Bacillus amyloliquefaciens B3 [31] . BLASTx analysis of the predicted open reading frames from this plasmid did not show any similarity to genetic loci involved in antibiotic resistance or virulence.…”
Section: Resultsmentioning
confidence: 99%
“…A plasmid was evident from strain AP143. High coverage contigs from the assembled genome sequence of AP143 (data not shown) were screened by BLASTn and one of the contigs showed high identity (99%) with plasmid pBSG3 from Bacillus amyloliquefaciens B3 [31] . BLASTx analysis of the predicted open reading frames from this plasmid did not show any similarity to genetic loci involved in antibiotic resistance or virulence.…”
Section: Resultsmentioning
confidence: 99%
“…8 ). Studies have shown that some species of the Bacillus genus produce antibiotics and fungal cell wall degrading enzymes such as chitinase and glucoamylase; while some species carry genes related to indole-3-acetic acid production and ferredoxin improving plant growth 55 58 . In addition, according to the analysis of bacterial functional analysis (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Additionally, peptides such as nisin and subtilin, encoded by nisB, nisC, and spaS, are bacteriocin effective against many Gram-positive organisms, functioning as probable probiotics with antimicrobial activities [67][68][69]. Moreover, B. subtilis SRCM103571 and SRCM103689 specifically possess genes encoding response regulators of aspartate phosphatase I and SaeR, which are involved in sporulation and adhesion to the host cells [70,71]. recombination, and repair; D, Cell cycle control, cell division, and chromosome partitioning; V, Defense mechanisms; T, Signal transduction mechanisms; M, Cell wall/membrane/envelope biogenesis; N, Cell motility; O, Posttranslational modification, protein turnover, and chaperones; C, Energy production and conversion; G, Carbohydrate transport and metabolism; E, Amino acid transport and metabolism; F, Nucleotide transport and metabolism; H, Coenzyme transport and metabolism; I, Lipid transport and metabolism; P, Inorganic ion transport and metabolism; Q, Secondary metabolite biosynthesis, transport, and catabolism.…”
Section: Comxmentioning
confidence: 99%