<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Molecular Microbiology – Erhardt lab, HU Berlin</title><link>https://www.molmicro.hu-berlin.de/news.html</link><atom:link href="https://www.molmicro.hu-berlin.de/news.xml" rel="self" type="application/rss+xml"/><description>Papers, preprints, grants and lab news from the Erhardt lab (Molecular Microbiology, Humboldt-Universität zu Berlin).</description><language>en</language><item><title><![CDATA[The Druantia defence system recognises single-stranded DNA]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-druantia</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-druantia</guid><pubDate>Tue, 22 Sep 2026 00:00:00 +0000</pubDate><category>Paper</category><description><![CDATA[Together with the groups of Markus Wahl and Chase Beisel, we characterised the compact type III-A Druantia system of <i>Escherichia coli</i>. Its two proteins, DruE and DruH, clear phage infections without harming the host cell. DruE forms a dimer that binds exposed single-stranded DNA and unwinds DNA with 3′-to-5′ directionality, using lock, wedge and clamp elements for strand separation. DruH interacts indirectly with DruE and other host proteins in uninfected cells; infection dissociates the complex. These results identify exposed single-stranded DNA as a trigger of bacterial immunity.]]></description></item><item><title><![CDATA[María José Giralt Zúñiga defended her PhD thesis]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-phd-giralt</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-phd-giralt</guid><pubDate>Mon, 24 Aug 2026 00:00:00 +0000</pubDate><category>Lab</category><description><![CDATA[María José Giralt Zúñiga defended her thesis “Cost-benefit trade-offs and evolutionary consequences of peritrichous flagellation in <i>Salmonella</i>”. Congratulations, Dr. Giralt Zúñiga.]]></description></item><item><title><![CDATA[Preprint: the cost-benefit trade-off of peritrichous flagellation]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-preprint-cost-benefit</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-preprint-cost-benefit</guid><pubDate>Thu, 20 Aug 2026 00:00:00 +0000</pubDate><category>Preprint</category><description><![CDATA[We expressed the flagellar master regulator <i>flhDC</i> of <i>Salmonella enterica</i> from inducible or constitutive promoters and obtained strains from nearly non-flagellated to hyperflagellated cells. More flagella reduced the growth rate: the flagellar share of the proteome grew mainly at the expense of ribosomes, and flagellin synthesis was the largest cost. More flagella also improved spreading, swimming speed and competitive fitness in structured environments. A proteome-allocation model predicts that the benefit of motility saturates near a flagellar investment of 3% of the proteome. Try the <a href="https://www.molmicro.hu-berlin.de/motility-simulation.html">interactive motility simulation</a>: strains with fewer or more flagella than the wild type swim side by side, in liquid and in agarose.]]></description></item><item><title><![CDATA[Preprint: BactoMate, a platform for the analysis of bacterial microscopy data]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-preprint-bactomate</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-preprint-bactomate</guid><pubDate>Thu, 06 Aug 2026 00:00:00 +0000</pubDate><category>Preprint</category><description><![CDATA[BactoMate is an open-source program with a graphical interface for microscopy data of bacteria. It combines file conversion, segmentation, quality control, fluorescence and foci quantification, cell tracking and lineage reconstruction in one workflow. The program records all parameters with the results, so that an analysis can be repeated with the same settings. The preprint shows applications to fluorescence imaging, swimming assays, microcolonies, phage infection and microfluidic time series.]]></description></item><item><title><![CDATA[Preprint: how nutrients set the number of flagella per cell]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-preprint-flagella-number</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-preprint-flagella-number</guid><pubDate>Fri, 10 Jul 2026 00:00:00 +0000</pubDate><category>Preprint</category><description><![CDATA[Together with the group of Haralampos Hatzikirou, we measured flagellar basal bodies in single <i>Salmonella</i> cells over time and described the data with a stochastic model. In the model, an RflP-dependent regulatory memory sets a target number of flagella, and synthesis, partitioning at division and growth determine the distribution around this target. The fitted model predicted the flagellar number in a nutrient condition that was not used for fitting.]]></description></item><item><title><![CDATA[Queuosine and i6A modifications of tRNATyr prevent frameshifting]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-trna</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-trna</guid><pubDate>Mon, 22 Jun 2026 00:00:00 +0000</pubDate><category>Paper</category><description><![CDATA[Together with the group of Ann Ehrenhofer-Murray, we analysed queuosine at the wobble position of tRNA<sup>Tyr</sup> and (ms<sup>2</sup>)i<sup>6</sup>A at position 37. <i>E. coli</i> that lacked both modifications showed a severe growth defect, increased +1 frameshifting at tyrosine codons and protein aggregation. The functional interplay is conserved in <i>Schizosaccharomyces pombe</i>.]]></description></item><item><title><![CDATA[Preprint: typhoidal Salmonella use preassembled flagella inside host cells]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-preprint-intracellular-flagella</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-preprint-intracellular-flagella</guid><pubDate>Tue, 16 Jun 2026 00:00:00 +0000</pubDate><category>Preprint</category><description><![CDATA[Together with the group of Michael Hensel, we followed the flagella that <i>Salmonella</i> assembles before it enters epithelial cells. The bacteria keep these flagella during invasion. Inside the <i>Salmonella</i>-containing vacuole the flagella are disassembled; in the cytosol, autophagy targets them. The human-restricted serovar Paratyphi A uses its preassembled flagella for motility inside the host cell and to escape from the vacuole.]]></description></item><item><title><![CDATA[Preprint: the last bacterial common ancestor encoded a complex flagellum]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-preprint-ancestral-flagellum</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-preprint-ancestral-flagellum</guid><pubDate>Fri, 12 Jun 2026 00:00:00 +0000</pubDate><category>Preprint</category><description><![CDATA[Only 24 flagellar genes were known to be conserved across bacteria. Together with the groups of Igor Zhulin, Morgan Beeby and Daniel Kearns, we searched a large set of bacterial genomes with profile- and sequence-based methods and gene-neighbourhood data. We found 28 more flagellar gene families that originated before the main diversification of bacteria. The ancestral flagellum thus had 52 genes, including the complete export apparatus, basal body, axial structures, stator units and regulatory checkpoints.]]></description></item><item><title><![CDATA[Preprint: molecular basis of the Druantia defence system]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-preprint-druantia-mechanism</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-preprint-druantia-mechanism</guid><pubDate>Wed, 13 May 2026 00:00:00 +0000</pubDate><category>Preprint</category><description><![CDATA[Together with the group of Nicholas Taylor, we studied a Druantia system that consists of only two proteins, DruH and DruE. The two proteins are sufficient for defence against phages. Cryo-EM structures show an asymmetric DruE dimer that unwinds double-stranded DNA with a 3′ overhang. DruH binds single-stranded DNA, and ATP at physiological concentrations inhibits this binding.]]></description></item><item><title><![CDATA[Structure of the sheathed flagellar filament of Vibrio alginolyticus]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-vibrio-sheath</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-vibrio-sheath</guid><pubDate>Thu, 23 Apr 2026 00:00:00 +0000</pubDate><category>Paper</category><description><![CDATA[In <i>Vibrio</i> species, a membranous sheath that extends from the outer membrane encloses the flagellar filament. Together with the group of Julien Bergeron, we combined cryo-EM, cryo-electron tomography and genetics to resolve the sheathed flagellum of <i>Vibrio alginolyticus</i>. The filament is a canonical 11-stranded supercoil of the flagellin FlaD2 inside a bilayered sheath. The filament surface is highly electronegative. This suggests that electrostatic repulsion between filament and sheath reduces friction during rotation. The cap protein FliD contains an additional domain that may coordinate sheath assembly with filament elongation.]]></description></item><item><title><![CDATA[Rosa Einenkel defended her PhD thesis]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-phd-einenkel</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-phd-einenkel</guid><pubDate>Fri, 17 Apr 2026 00:00:00 +0000</pubDate><category>Lab</category><description><![CDATA[Rosa Einenkel defended her thesis “Structural and mechanistic insights into assembly and function of bacterial flagella”. Congratulations, Dr. Einenkel.]]></description></item><item><title><![CDATA[Structure of a contractile injection system of Salmonella enterica subsp. salamae]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-ecis</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-ecis</guid><pubDate>Thu, 16 Apr 2026 00:00:00 +0000</pubDate><category>Paper</category><description><![CDATA[Extracellular contractile injection systems are phage-derived nanomachines that deliver effectors into target cells. Together with the group of Nicholas Taylor, we determined the cryo-EM structure of the system encoded by <i>S. enterica</i> subsp. <i>salamae</i>. The structure shows a sheath architecture that differs from that of other contractile injection systems, a cage-like shell around the central spike and an associated integral membrane protein. Our data indicate that the system interacts with the inner membrane. Based on these structural features, we identified a previously unannotated cluster of contractile injection systems.]]></description></item><item><title><![CDATA[Preprint: crystal structure of the flagellin of E. coli Nissle 1917]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2026-preprint-nissle-flagellin</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2026-preprint-nissle-flagellin</guid><pubDate>Mon, 30 Mar 2026 00:00:00 +0000</pubDate><category>Preprint</category><description><![CDATA[Together with the groups of Alexander Weber and Michael Hensel, we contributed to the analysis of the flagellin FliC of the probiotic strain <i>E. coli</i> Nissle 1917. Its crystal structure at 1.2 Å shows a hypervariable region that forms an outer domain around the conserved filament core. Removal of the linker to this region reduced protein stability and motility, whereas recognition by TLR5 changed only moderately.]]></description></item><item><title><![CDATA[Conjugative pili restructure biofilms]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2025-conjugation</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2025-conjugation</guid><pubDate>Mon, 15 Dec 2025 00:00:00 +0000</pubDate><category>Paper</category><description><![CDATA[Together with the group of Carey Nadell, we followed transfer of the F-like plasmid pED208 inside <i>E. coli</i> biofilms in microfluidic chambers. Conjugation was efficient until the cell density reached a threshold associated with high matrix secretion. Conjugative pili enabled matrix-deficient cells to form dense biofilms with increased antibiotic and phage tolerance. Plasmid-carrying cells dispersed less than plasmid-free cells.]]></description></item><item><title><![CDATA[FliI ATPase activity is required for timely substrate switching]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2025-flii</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2025-flii</guid><pubDate>Fri, 05 Dec 2025 00:00:00 +0000</pubDate><category>Paper</category><description><![CDATA[The flagellar type-III secretion system exports its building blocks in a defined order. Rosa Einenkel analysed <i>Salmonella</i> strains with mutations in the catalytic domain of the ATPase FliI. Minimal ATPase activity was sufficient for early export and hook-basal-body assembly. Efficient substrate-specificity switching and export of late substrates required near-wild-type activity. The mutants showed delayed class 3 gene expression, prolonged early secretion and impaired filament assembly, although FliI localisation and oligomerisation were normal. These data link ATPase activity to substrate switching in type-III secretion.]]></description></item><item><title><![CDATA[Einstein Foundation funds a Berlin/HUJI research project]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2025-einstein</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2025-einstein</guid><pubDate>Wed, 03 Dec 2025 00:00:00 +0000</pubDate><category>Grant</category><description><![CDATA[The Einstein Foundation Berlin approved our Einstein Berlin/HUJI research project (BJ-2025-857) with the group of Orna Amster-Choder at the Hebrew University of Jerusalem.]]></description></item><item><title><![CDATA[Review on regulation, assembly and function of the flagellum]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2025-mmbr</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2025-mmbr</guid><pubDate>Thu, 20 Nov 2025 00:00:00 +0000</pubDate><category>Review</category><description><![CDATA[Our review in <i>Microbiology and Molecular Biology Reviews</i> covers recent progress on the structure, assembly and regulation of the flagellum: hierarchical gene regulation, motor mechanics and new structures of the core components. The review also discusses the legacy of Howard Berg and open questions that require single-cell observations.]]></description></item><item><title><![CDATA[DFG funding in SPP 2389 for research on conjugative pili in biofilms]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2025-spp2389</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2025-spp2389</guid><pubDate>Fri, 22 Aug 2025 00:00:00 +0000</pubDate><category>Grant</category><description><![CDATA[The DFG funds our project “Conjugative pili shape spatial and functional differentiation in multicellular bacterial biofilms” in the priority programme SPP 2389 “Emergent functions of bacterial multicellularity” for three years.]]></description></item><item><title><![CDATA[FliO is a conserved core component of the flagellar type-III secretion system]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2025-flio</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2025-flio</guid><pubDate>Thu, 21 Aug 2025 00:00:00 +0000</pubDate><category>Paper</category><description><![CDATA[Together with the groups of Igor Zhulin and David Hendrixson, we searched more than 30,000 representative bacterial genomes for FliO, a protein that is poorly conserved at the sequence level. FliO is present in about 95% of genomes that encode the export-gate proteins FliP, FliQ and FliR. This suggests that FliO is an ancestral core component of the flagellar type-III secretion system. About 40% of bacterial genomes contain flagellar genes. In <i>Campylobacter jejuni</i>, FliO and its AMIN domain are needed for efficient flagellation, stability of FlhB and host colonisation.]]></description></item><item><title><![CDATA[YebC enhances translation of proline-rich motifs]]></title><link>https://www.molmicro.hu-berlin.de/news.html#2025-yebc</link><guid isPermaLink="true">https://www.molmicro.hu-berlin.de/news.html#2025-yebc</guid><pubDate>Mon, 07 Jul 2025 00:00:00 +0000</pubDate><category>Paper</category><description><![CDATA[Together with the group of Emmanuelle Charpentier, we identified the conserved RNA-binding protein YebC as a translation factor. YebC interacts with 23S rRNA near the peptidyl-transferase centre. In the absence of YebC, ribosome pausing at proline-rich motifs increased in <i>Streptococcus pyogenes</i>. Experiments in <i>Salmonella</i> Typhimurium and in an in vitro translation system support this function.]]></description></item></channel></rss>
