Functionally uncharacterized UPF0118 family has been re-designated as autoinducer-2 exporter (AI-2E) family since one of its members, YdgG, was identified to function as an AI-2E. However, it's very likely that AI-2E family members may exhibit significantly distinct functions due to low identities between them. Recently, we identified one member of this family designated as UPF0118 to represent a novel class of Na(Li)/H antiporters. In this study, we presented that UPF0118, together with its homologs, should represent an independent group of AI-2E family, designated as Na/H Antiporter Group. Notably, this group shows five highly conserved motifs designated as Motifs A to E, which are not detected in the majority of AI-2E family members. Functional analysis established that polar or charged residues located in Motif A to D play a vital role in Na(Li)/H antiport activity or pH response of UPF0118. However, three basic residues located in Motif E are not involved in the function of UPF0118, although the truncation of C terminus resulted in the non-expression of this transporter. Therefore, we propose that E-R-K-Q-D-R-R-E-K-S located in Motifs A to D can be used for signature functional motifs to recognize whether AI-2E family members function as Na(Li)/H antiporters. Current findings positively contribute to the knowledge of molecular mechanism of Na, Li transporting and pH response of UPF0118, and the functional prediction of uncharacterized AI-2E family members.
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http://dx.doi.org/10.3389/fmicb.2020.00841 | DOI Listing |
Front Microbiol
May 2022
State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-Products, Ningbo University, Ningbo, China.
The function of the autoinducer-2 exporters (AI-2E) family transporter protein of is still unclear. The phylogenetic analysis was used to analyze the relationship between the AI-2E protein of the CICC 6074 strain and other AI-2E family members. KNabc strain was used to verify whether the protein has Na (Li)/H antiporter activity.
View Article and Find Full Text PDFInt J Mol Sci
March 2022
Infectious Diseases Translational Research Program, Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117545, Singapore.
The presence of co-infections or superinfections with bacterial pathogens in COVID-19 patients is associated with poor outcomes, including increased morbidity and mortality. We hypothesized that SARS-CoV-2 and its components interact with the biofilms generated by commensal bacteria, which may contribute to co-infections. This study employed crystal violet staining and particle-tracking microrheology to characterize the formation of biofilms by and that commonly cause secondary bacterial pneumonia.
View Article and Find Full Text PDFFront Microbiol
May 2020
Shanghai Engineering Research Center of Aquatic Product Processing & Preservation, Shanghai Ocean University, Shanghai, China.
Food spoilage by certain species of bacteria is reported to be regulated by quorum sensing (QS). and , the major specific spoilage organisms, are found to be limited in their QS and co-culture interactions. The aim of this study was to determine how QS-regulated proteins affect the spoilage potential of co-cultured and obtained from spoiled bigeye tuna () using a proteomics approach.
View Article and Find Full Text PDFFront Microbiol
May 2020
Department of Microbiology and Biotechnology, College of Biological Sciences, Northeast Agricultural University, Harbin, China.
Functionally uncharacterized UPF0118 family has been re-designated as autoinducer-2 exporter (AI-2E) family since one of its members, YdgG, was identified to function as an AI-2E. However, it's very likely that AI-2E family members may exhibit significantly distinct functions due to low identities between them. Recently, we identified one member of this family designated as UPF0118 to represent a novel class of Na(Li)/H antiporters.
View Article and Find Full Text PDFJ Mol Microbiol Biotechnol
December 2010
Division of Biological Sciences, University of California at San Diego, La Jolla, CA 92093-0116, USA.
The TqsA (YdgG) protein of Escherichia coli has been shown to export the autoinducer-2 (AI-2) molecule, a furanosyl borate diester that bears little resemblance to previously characterized biological molecules. TqsA belongs to a large superfamily, the AI-2 exporter (AI-2E) superfamily, of putative transporters with no other functionally characterized members. These proteins derive exclusively from bacteria.
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