{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,5]],"date-time":"2026-05-05T02:54:04Z","timestamp":1777949644850,"version":"3.51.4"},"reference-count":48,"publisher":"American Society for Microbiology","issue":"9","license":[{"start":{"date-parts":[[2025,9,18]],"date-time":"2025-09-18T00:00:00Z","timestamp":1758153600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2025,9,18]],"date-time":"2025-09-18T00:00:00Z","timestamp":1758153600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"name":"FDA\/CBER intramural program","award":["none"],"award-info":[{"award-number":["none"]}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Bacteriol"],"published-print":{"date-parts":[[2025,9,18]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      Zinc is a critical nutrient for all living organisms, including bacterial pathogens such as\n                      <jats:italic toggle=\"yes\">Corynebacterium diphtheriae<\/jats:italic>\n                      , the causative agent of the severe human respiratory disease diphtheria. As such, zinc acquisition is essential for many pathogens to cause disease. We previously showed that the zinc-regulated ABC transporter encoded by the\n                      <jats:italic toggle=\"yes\">znu<\/jats:italic>\n                      locus is one of several zinc uptake systems that support the growth of\n                      <jats:italic toggle=\"yes\">C. diphtheriae<\/jats:italic>\n                      in zinc-limited medium. In this study, we examine the function and cellular localization of components encoded by the\n                      <jats:italic toggle=\"yes\">znu<\/jats:italic>\n                      gene cluster, which includes the ZnuABC transporter and the novel membrane and cell wall proteins ZnuE, ZnuF, and ZnuG. Deletion of\n                      <jats:italic toggle=\"yes\">znuE<\/jats:italic>\n                      results in reduced growth in zinc-limited media, suggesting a role in zinc uptake. While the growth of\n                      <jats:italic toggle=\"yes\">znuF<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">znuG<\/jats:italic>\n                      mutants was not affected in zinc-limited medium, deletion of these two genes in a mutant also lacking the\n                      <jats:italic toggle=\"yes\">znuABC<\/jats:italic>\n                      transporter restored growth to wild-type levels, suggesting that ZnuF and ZnuG exert an unusual modulating effect on zinc import. ZnuE, ZnuF, and ZnuG possess a unique motif that is associated with Zn binding as demonstrated by thermal shift assays, targeted mutagenesis, and structural analysis. Although ZnuF and ZnuG are both present in the cell wall, only ZnuG contains a sortase recognition signal that is critical for localizing proteins to the cell wall. Furthermore, ZnuF localization does not require any of the six known sortase enzymes in\n                      <jats:italic toggle=\"yes\">C. diphtheriae<\/jats:italic>\n                      , suggesting a novel localization mechanism.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>IMPORTANCE<\/jats:title>\n                    <jats:p>\n                      Zinc is a critical nutrient required by many bacterial pathogens. While the function of multiple zinc importer systems has been previously characterized in\n                      <jats:italic toggle=\"yes\">Corynebacterium diphtheriae<\/jats:italic>\n                      , the transporter encoded by the\n                      <jats:italic toggle=\"yes\">znu<\/jats:italic>\n                      gene cluster includes components not found in other metal transport systems. In this report, we examined the roles of three components of the\n                      <jats:italic toggle=\"yes\">znu<\/jats:italic>\n                      gene cluster, ZnuE, ZnuF, and ZnuG, and show that these proteins all possess a putative zinc-binding domain and have varying effects on growth in zinc-limited medium. Additionally, ZnuF uses a novel mechanism for cell wall localization. This study further expands our understanding of\n                      <jats:italic toggle=\"yes\">C. diphtheriae<\/jats:italic>\n                      zinc import and points to a potentially novel mechanism for the localization of cell wall proteins.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1128\/jb.00239-25","type":"journal-article","created":{"date-parts":[[2025,8,18]],"date-time":"2025-08-18T13:00:58Z","timestamp":1755522058000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["Analysis of novel zinc-binding proteins in the cell wall of\n                    <i>Corynebacterium diphtheriae<\/i>"],"prefix":"10.1128","volume":"207","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3060-7095","authenticated-orcid":false,"given":"Eric D.","family":"Peng","sequence":"first","affiliation":[{"name":"Laboratory of Respiratory and Special Pathogens, Division of Bacterial, Parasitic, and Allergenic Products, Center for Biologics Evaluation and Research, Food and Drug Administration","place":["Silver Spring, USA"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lindsey R.","family":"Lyman","sequence":"additional","affiliation":[{"name":"Laboratory of Respiratory and Special Pathogens, Division of Bacterial, Parasitic, and Allergenic Products, Center for Biologics Evaluation and Research, Food and Drug Administration","place":["Silver Spring, USA"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1516-7925","authenticated-orcid":true,"given":"Michael P.","family":"Schmitt","sequence":"additional","affiliation":[{"name":"Laboratory of Respiratory and Special Pathogens, Division of Bacterial, Parasitic, and Allergenic Products, Center for Biologics Evaluation and Research, Food and Drug Administration","place":["Silver Spring, USA"]}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"235","reference":[{"key":"e_1_3_3_2_2","doi-asserted-by":"publisher","DOI":"10.1021\/pr0603699"},{"key":"e_1_3_3_3_2","doi-asserted-by":"publisher","DOI":"10.1007\/978-1-4939-9030-6_18"},{"key":"e_1_3_3_4_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.cbpa.2009.11.008"},{"key":"e_1_3_3_5_2","doi-asserted-by":"publisher","DOI":"10.1038\/s41579-022-00745-6"},{"key":"e_1_3_3_6_2","doi-asserted-by":"publisher","DOI":"10.1111\/mmi.12504"},{"key":"e_1_3_3_7_2","doi-asserted-by":"publisher","DOI":"10.1128\/mBio.01281-17"},{"key":"e_1_3_3_8_2","doi-asserted-by":"publisher","DOI":"10.1128\/mSphere.00061-20"},{"key":"e_1_3_3_9_2","doi-asserted-by":"publisher","DOI":"10.1128\/jb.00124-24"},{"key":"e_1_3_3_10_2","doi-asserted-by":"publisher","DOI":"10.1128\/JB.00051-18"},{"key":"e_1_3_3_11_2","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0221711"},{"key":"e_1_3_3_12_2","doi-asserted-by":"publisher","DOI":"10.1128\/JB.00274-21"},{"key":"e_1_3_3_13_2","doi-asserted-by":"publisher","DOI":"10.1128\/JB.185.23.6826-6840.2003"},{"key":"e_1_3_3_14_2","doi-asserted-by":"publisher","DOI":"10.1111\/mmi.12693"},{"key":"e_1_3_3_15_2","doi-asserted-by":"publisher","DOI":"10.1002\/j.1460-2075.1993.tb06169.x"},{"key":"e_1_3_3_16_2","first-page":"28","article-title":"Fitting a mixture model by expectation maximization to discover motifs in biopolymers","volume":"2","author":"Bailey TL","year":"1994","unstructured":"Bailey TL, Elkan C. 1994. 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