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Efficient Exploitation of Multiple Novel Bacteriocins by Combination of Complete Genome and Peptidome

Backgroud: The growing emergence of antibiotic-resistant pathogens including the most dangerous superbugs requires quick discovery of novel antibiotics/biopreservatives for human health and food safety. Bacteriocins, a subgroup of antimicrobial peptides, have been considered as promising alternative...

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Autores principales: Yi, Lanhua, Luo, Lingli, Lü, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053492/
https://www.ncbi.nlm.nih.gov/pubmed/30057579
http://dx.doi.org/10.3389/fmicb.2018.01567
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author Yi, Lanhua
Luo, Lingli
Lü, Xin
author_facet Yi, Lanhua
Luo, Lingli
Lü, Xin
author_sort Yi, Lanhua
collection PubMed
description Backgroud: The growing emergence of antibiotic-resistant pathogens including the most dangerous superbugs requires quick discovery of novel antibiotics/biopreservatives for human health and food safety. Bacteriocins, a subgroup of antimicrobial peptides, have been considered as promising alternatives to antibiotics. Abundant novel bacteriocins are stored in genome sequences of lactic acid bacteria. However, discovery of novel bacteriocins still mainly relies on dubious traditional purification with low efficiency. Moreover, sequence alignment is invalid for novel bacteriocins which have no homology to known bacteriocins in databases. Therefore, an efficient, simple, universal, and time-saving method was needed to discover novel bacteriocins. Methods and Results: Crude bacteriocins from both cell-related and culture supernatant of Lactobacillus crustorum MN047 fermentation were applied to LC-MS/MS for peptidome assay, by which 131 extracellular peptides or proteins were identified in the complete genome sequence of L. crustorum MN047. Further, the genes of suspected bacteriocins were verified by expressed in Escherichia coli BL21 (DE3) pLysS. Thereafter, eight novel bacteriocins and two nonribosomal antimicrobial peptides were identified to be broad-spectrum activity against both Gram-positive and Gram-negative bacteria, including some multidrug-resistant strains. Among them, BM1556 located within predicted bacteriocin gene cluster. The most active bacteriocin BM1122 had low MIC values of 13.7 mg/L against both Staphylococcus aureus ATCC29213 and E. coli ATCC25922. The BM1122 had bactericidal action mode by biofilm-destruction, pore-formation, and membrane permeability change. Conclusions: The combination of complete genome and peptidome is a valid approach for quick discovery of novel bacteriocins without/with-low homology to known ones. This method will contribute to deep exploitation of novel bacteriocins in genome of bacteria submitted to GenBank.
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spelling pubmed-60534922018-07-27 Efficient Exploitation of Multiple Novel Bacteriocins by Combination of Complete Genome and Peptidome Yi, Lanhua Luo, Lingli Lü, Xin Front Microbiol Microbiology Backgroud: The growing emergence of antibiotic-resistant pathogens including the most dangerous superbugs requires quick discovery of novel antibiotics/biopreservatives for human health and food safety. Bacteriocins, a subgroup of antimicrobial peptides, have been considered as promising alternatives to antibiotics. Abundant novel bacteriocins are stored in genome sequences of lactic acid bacteria. However, discovery of novel bacteriocins still mainly relies on dubious traditional purification with low efficiency. Moreover, sequence alignment is invalid for novel bacteriocins which have no homology to known bacteriocins in databases. Therefore, an efficient, simple, universal, and time-saving method was needed to discover novel bacteriocins. Methods and Results: Crude bacteriocins from both cell-related and culture supernatant of Lactobacillus crustorum MN047 fermentation were applied to LC-MS/MS for peptidome assay, by which 131 extracellular peptides or proteins were identified in the complete genome sequence of L. crustorum MN047. Further, the genes of suspected bacteriocins were verified by expressed in Escherichia coli BL21 (DE3) pLysS. Thereafter, eight novel bacteriocins and two nonribosomal antimicrobial peptides were identified to be broad-spectrum activity against both Gram-positive and Gram-negative bacteria, including some multidrug-resistant strains. Among them, BM1556 located within predicted bacteriocin gene cluster. The most active bacteriocin BM1122 had low MIC values of 13.7 mg/L against both Staphylococcus aureus ATCC29213 and E. coli ATCC25922. The BM1122 had bactericidal action mode by biofilm-destruction, pore-formation, and membrane permeability change. Conclusions: The combination of complete genome and peptidome is a valid approach for quick discovery of novel bacteriocins without/with-low homology to known ones. This method will contribute to deep exploitation of novel bacteriocins in genome of bacteria submitted to GenBank. Frontiers Media S.A. 2018-07-13 /pmc/articles/PMC6053492/ /pubmed/30057579 http://dx.doi.org/10.3389/fmicb.2018.01567 Text en Copyright © 2018 Yi, Luo and Lü. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Yi, Lanhua
Luo, Lingli
Lü, Xin
Efficient Exploitation of Multiple Novel Bacteriocins by Combination of Complete Genome and Peptidome
title Efficient Exploitation of Multiple Novel Bacteriocins by Combination of Complete Genome and Peptidome
title_full Efficient Exploitation of Multiple Novel Bacteriocins by Combination of Complete Genome and Peptidome
title_fullStr Efficient Exploitation of Multiple Novel Bacteriocins by Combination of Complete Genome and Peptidome
title_full_unstemmed Efficient Exploitation of Multiple Novel Bacteriocins by Combination of Complete Genome and Peptidome
title_short Efficient Exploitation of Multiple Novel Bacteriocins by Combination of Complete Genome and Peptidome
title_sort efficient exploitation of multiple novel bacteriocins by combination of complete genome and peptidome
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053492/
https://www.ncbi.nlm.nih.gov/pubmed/30057579
http://dx.doi.org/10.3389/fmicb.2018.01567
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