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	<front>
		<article-meta>
		    <article-id pub-id-type="doi">10.3390/ijms22105328</article-id>		    
		    <title-group>
		        <article-title>MexAB-OprM Efflux Pump Interaction with the Peptidoglycan of <i>Escherichia coli</i> and <i>Pseudomonas aeruginosa</i></article-title>
		    </title-group>
		    <contrib-group>
		    			    			    			        <contrib contrib-type="author" corresp="no">
		            		            <name>
		                <surname>Ma</surname>
		                <given-names>Miao</given-names>
		                <prefix>Dr.</prefix>
		            </name>
		            		            		            	
		            <aff>		                
		                Laboratoire CiTCoM, Université de Paris, CNRS, 75006 Paris, France
		            </aff>		            
		        		
		            <aff>		                
		                Department of Biochemistry, University of Cambridge, Cambridge CB2 1GA, UK
		            </aff>		            
		        			        			        			            	<email>mm2303@cam.ac.uk</email>
		            		        </contrib>
		    			        <contrib contrib-type="author" corresp="no">
		            		            <name>
		                <surname>Lustig</surname>
		                <given-names>Margaux</given-names>
		                <prefix>Dr.</prefix>
		            </name>
		            		            		            	
		            <aff>		                
		                Laboratoire CiTCoM, Université de Paris, CNRS, 75006 Paris, France
		            </aff>		            
		        			        			        			            	<email>margaux.lustig@parisdescartes.fr</email>
		            		        </contrib>
		    			        <contrib contrib-type="author" corresp="no">
		            		            <name>
		                <surname>Salem</surname>
		                <given-names>Michèle</given-names>
		                <prefix>Dr.</prefix>
		            </name>
		            		            		            	
		            <aff>		                
		                Laboratoire CiTCoM, Université de Paris, CNRS, 75006 Paris, France
		            </aff>		            
		        			        			        			            	<email>michele.salem@u-paris.fr</email>
		            		        </contrib>
		    			        <contrib contrib-type="author" corresp="no">
		            		            <contrib-id contrib-id-type="orcid">http://orcid.org/0000-0003-3205-0275</contrib-id>
		        			            <name>
		                <surname>Mengin-Lecreulx</surname>
		                <given-names>Dominique</given-names>
		                <prefix>Dr.</prefix>
		            </name>
		            		            		            	
		            <aff>		                
		                Institute for Integrative Biology of the Cell (I2BC), Université Paris-Saclay, CEA, CNRS, 91198 Gif-sur-Yvette, France
		            </aff>		            
		        			        			        			            	<email>dominique.mengin-lecreulx@i2bc.paris-saclay.fr</email>
		            		        </contrib>
		    			        <contrib contrib-type="author" corresp="no">
		            		            <contrib-id contrib-id-type="orcid">http://orcid.org/0000-0001-9683-4453</contrib-id>
		        			            <name>
		                <surname>Phan</surname>
		                <given-names>Gilles</given-names>
		                <prefix>Dr.</prefix>
		            </name>
		            		            		            	
		            <aff>		                
		                Laboratoire CiTCoM, Université de Paris, CNRS, 75006 Paris, France
		            </aff>		            
		        			        			        			            	<email>gilles.phan@u-paris.fr</email>
		            		        </contrib>
		    			        <contrib contrib-type="author" corresp="yes">
		            		            <contrib-id contrib-id-type="orcid">http://orcid.org/0000-0001-9862-1232</contrib-id>
		        			            <name>
		                <surname>Broutin</surname>
		                <given-names>Isabelle</given-names>
		                <prefix>Dr.</prefix>
		            </name>
		            		            		            	
		            <aff>		                
		                Laboratoire CiTCoM, Université de Paris, CNRS, 75006 Paris, France
		            </aff>		            
		        			        			        			            	<email>isabelle.broutin@u-paris.fr</email>
		            		        </contrib>
		    			    		        
		    </contrib-group>
		    <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2021-05-18">
		        <day>18</day>
		        <month>05</month>
		        <year>2021</year>
		    </pub-date>
		    <volume>22</volume>
		    <issue>10</issue>
		    <history>
		        <date date-type="accepted" iso-8601-date="2021-05-12">
		            <day>12</day>
		            <month>05</month>
		            <year>2021</year>
		        </date>
		    </history>
		    			<elocation-id>e5328</elocation-id>
					    <abstract>
		    	One of the major families of membrane proteins found in prokaryote genome corresponds to the transporters. Among them, the resistance-nodulation-cell division (RND) transporters are highly studied, as being responsible for one of the most problematic mechanisms used by bacteria to resist to antibiotics, i.e., the active efflux of drugs. In Gram-negative bacteria, these proteins are inserted in the inner membrane and form a tripartite assembly with an outer membrane factor and a periplasmic linker in order to cross the two membranes to expulse molecules outside of the cell. A lot of information has been collected to understand the functional mechanism of these pumps, especially with AcrAB-TolC from <i>Escherichia coli</i>, but one missing piece from all the suggested models is the role of peptidoglycan in the assembly. Here, by pull-down experiments with purified peptidoglycans, we precise the MexAB-OprM interaction with the peptidoglycan from <i>Escherichia coli</i> and <i>Pseudomonas aeruginosa</i>, highlighting a role of the peptidoglycan in stabilizing the MexA-OprM complex and also differences between the two Gram-negative bacteria peptidoglycans.
		    </abstract>		     	        
	        		    <funding-group>
		    			        <award-group id="501100001665"> 
		            <funding-source country="">Agence Nationale de la Recherche</funding-source>
		            		            <award-id>ANR-12-BSV8-0010</award-id>
		        			            <award-id>ANR-17-CE11-0028-02</award-id>
		        			        </award-group>
		    			    </funding-group>
						<permissions>
	            <copyright-statement>
	            	&#169; 1996-2021 MDPI (Basel, Switzerland)
	            </copyright-statement>
	            <copyright-year>2021</copyright-year>
	            <copyright-holder></copyright-holder>
	            <license xlink:href="https://creativecommons.org/licenses/by/4.0/">
	               <license-p>
	               		This is an open access article distributed under the <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank" rel="noopener noreferrer">Creative Commons Attribution License</a> which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited
	               </license-p>
	            </license>
			</permissions>
						<kwd-group kwd-group-type="author-keywords">
            	<title>Keywords</title>
            	            	<kwd>membrane</kwd>
            	            	<kwd>peptidoglycan</kwd>
            	            	<kwd>efflux pump assembly</kwd>
            	            	<kwd>resistance</kwd>
            	            	<kwd><i>Pseudomonas</i></kwd>
            		            
			</kwd-group>
					</article-meta>
	    <journal-meta>
	        <journal-title-group>
	            <journal-title>International Journal of Molecular Sciences</journal-title>
	            <abbrev-journal-title>Int J Mol Sci</abbrev-journal-title>
	        </journal-title-group>
	        <issn publication-format="electronic">1422-0067</issn>
	        <publisher>
	        	<publisher-name>MDPI</publisher-name>
	        </publisher>
	    </journal-meta>	    
	</front>
</article>

