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Alanine racemase is essential for the growth and interspecies competitiveness of Streptococcus mutans

D-alanine (D-Ala) is an essential amino acid that has a key role in bacterial cell wall synthesis. Alanine racemase (Alr) is a unique enzyme that interconverts L-alanine and D-alanine in most bacteria, making this enzyme a potential target for antimicrobial drug development. Streptococcus mutans is...

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Autores principales: Wei, Yuan, Qiu, Wei, Zhou, Xue-Dong, Zheng, Xin, Zhang, Ke-Ke, Wang, Shi-Da, Li, Yu-Qing, Cheng, Lei, Li, Ji-Yao, Xu, Xin, Li, Ming-Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168415/
https://www.ncbi.nlm.nih.gov/pubmed/27740612
http://dx.doi.org/10.1038/ijos.2016.34
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author Wei, Yuan
Qiu, Wei
Zhou, Xue-Dong
Zheng, Xin
Zhang, Ke-Ke
Wang, Shi-Da
Li, Yu-Qing
Cheng, Lei
Li, Ji-Yao
Xu, Xin
Li, Ming-Yun
author_facet Wei, Yuan
Qiu, Wei
Zhou, Xue-Dong
Zheng, Xin
Zhang, Ke-Ke
Wang, Shi-Da
Li, Yu-Qing
Cheng, Lei
Li, Ji-Yao
Xu, Xin
Li, Ming-Yun
author_sort Wei, Yuan
collection PubMed
description D-alanine (D-Ala) is an essential amino acid that has a key role in bacterial cell wall synthesis. Alanine racemase (Alr) is a unique enzyme that interconverts L-alanine and D-alanine in most bacteria, making this enzyme a potential target for antimicrobial drug development. Streptococcus mutans is a major causative factor of dental caries. The factors involved in the survival, virulence and interspecies interactions of S. mutans could be exploited as potential targets for caries control. The current study aimed to investigate the physiological role of Alr in S. mutans. We constructed alr mutant strain of S. mutans and evaluated its phenotypic traits and interspecies competitiveness compared with the wild-type strain. We found that alr deletion was lethal to S. mutans. A minimal supplement of D-Ala (150 μg·mL(−1)) was required for the optimal growth of the alr mutant. The depletion of D-alanine in the growth medium resulted in cell wall perforation and cell lysis in the alr mutant strain. We also determined the compromised competitiveness of the alr mutant strain relative to the wild-type S. mutans against other oral streptococci (S. sanguinis or S. gordonii), demonstrated using either conditioned medium assays or dual-species fluorescent in situ hybridization analysis. Given the importance and necessity of alr to the growth and competitiveness of S. mutans, Alr may represent a promising target to modulate the cariogenicity of oral biofilms and to benefit the management of dental caries.
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spelling pubmed-51684152016-12-21 Alanine racemase is essential for the growth and interspecies competitiveness of Streptococcus mutans Wei, Yuan Qiu, Wei Zhou, Xue-Dong Zheng, Xin Zhang, Ke-Ke Wang, Shi-Da Li, Yu-Qing Cheng, Lei Li, Ji-Yao Xu, Xin Li, Ming-Yun Int J Oral Sci Original Article D-alanine (D-Ala) is an essential amino acid that has a key role in bacterial cell wall synthesis. Alanine racemase (Alr) is a unique enzyme that interconverts L-alanine and D-alanine in most bacteria, making this enzyme a potential target for antimicrobial drug development. Streptococcus mutans is a major causative factor of dental caries. The factors involved in the survival, virulence and interspecies interactions of S. mutans could be exploited as potential targets for caries control. The current study aimed to investigate the physiological role of Alr in S. mutans. We constructed alr mutant strain of S. mutans and evaluated its phenotypic traits and interspecies competitiveness compared with the wild-type strain. We found that alr deletion was lethal to S. mutans. A minimal supplement of D-Ala (150 μg·mL(−1)) was required for the optimal growth of the alr mutant. The depletion of D-alanine in the growth medium resulted in cell wall perforation and cell lysis in the alr mutant strain. We also determined the compromised competitiveness of the alr mutant strain relative to the wild-type S. mutans against other oral streptococci (S. sanguinis or S. gordonii), demonstrated using either conditioned medium assays or dual-species fluorescent in situ hybridization analysis. Given the importance and necessity of alr to the growth and competitiveness of S. mutans, Alr may represent a promising target to modulate the cariogenicity of oral biofilms and to benefit the management of dental caries. Nature Publishing Group 2016-12 2016-10-14 /pmc/articles/PMC5168415/ /pubmed/27740612 http://dx.doi.org/10.1038/ijos.2016.34 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Wei, Yuan
Qiu, Wei
Zhou, Xue-Dong
Zheng, Xin
Zhang, Ke-Ke
Wang, Shi-Da
Li, Yu-Qing
Cheng, Lei
Li, Ji-Yao
Xu, Xin
Li, Ming-Yun
Alanine racemase is essential for the growth and interspecies competitiveness of Streptococcus mutans
title Alanine racemase is essential for the growth and interspecies competitiveness of Streptococcus mutans
title_full Alanine racemase is essential for the growth and interspecies competitiveness of Streptococcus mutans
title_fullStr Alanine racemase is essential for the growth and interspecies competitiveness of Streptococcus mutans
title_full_unstemmed Alanine racemase is essential for the growth and interspecies competitiveness of Streptococcus mutans
title_short Alanine racemase is essential for the growth and interspecies competitiveness of Streptococcus mutans
title_sort alanine racemase is essential for the growth and interspecies competitiveness of streptococcus mutans
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168415/
https://www.ncbi.nlm.nih.gov/pubmed/27740612
http://dx.doi.org/10.1038/ijos.2016.34
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