Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/172220
Title: | Cyclic-di-AMP signalling in lactic acid bacteria | Authors: | Turner, Mark S. Xiang, Yuwei Liang, Zhao-Xun Marcellin, Esteban Pham, Huong Thi |
Keywords: | Science::Biological sciences | Issue Date: | 2023 | Source: | Turner, M. S., Xiang, Y., Liang, Z., Marcellin, E. & Pham, H. T. (2023). Cyclic-di-AMP signalling in lactic acid bacteria. FEMS Microbiology Reviews, 47(3), 1-16. https://dx.doi.org/10.1093/femsre/fuad025 | Journal: | FEMS Microbiology Reviews | Abstract: | Cyclic dimeric adenosine monophosphate (cyclic-di-AMP) is a nucleotide second messenger present in Gram-positive bacteria, Gram-negative bacteria and some Archaea. The intracellular concentration of cyclic-di-AMP is adjusted in response to environmental and cellular cues, primarily through the activities of synthesis and degradation enzymes. It performs its role by binding to protein and riboswitch receptors, many of which contribute to osmoregulation. Imbalances in cyclic-di-AMP can lead to pleiotropic phenotypes, affecting aspects such as growth, biofilm formation, virulence, and resistance to osmotic, acid, and antibiotic stressors. This review focuses on cyclic-di-AMP signalling in lactic acid bacteria (LAB) incorporating recent experimental discoveries and presenting a genomic analysis of signalling components from a variety of LAB, including those found in food, and commensal, probiotic, and pathogenic species. All LAB possess enzymes for the synthesis and degradation of cyclic-di-AMP, but are highly variable with regards to the receptors they possess. Studies in Lactococcus and Streptococcus have revealed a conserved function for cyclic-di-AMP in inhibiting the transport of potassium and glycine betaine, either through direct binding to transporters or to a transcriptional regulator. Structural analysis of several cyclic-di-AMP receptors from LAB has also provided insights into how this nucleotide exerts its influence. | URI: | https://hdl.handle.net/10356/172220 | ISSN: | 0168-6445 | DOI: | 10.1093/femsre/fuad025 | Schools: | School of Biological Sciences | Rights: | © The Author(s) 2023. Published by Oxford University Press on behalf of FEMS. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SBS Journal Articles |
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fuad025.pdf | 2.29 MB | Adobe PDF | ![]() View/Open |
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