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581“…Recent high-precision single-cell measurements showed that, at least in bacteria, switching in gene states is slow relative to the typical rates of active transcription and translation. Hence using the lac operon as an archetype, in such a region of operon-state switching, we present a fluctuating-rate model for this classical gene regulation module, incorporating the more realistic operon-state switching mechanism that was recently elucidated. …”
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582por Sampath, Vinaya“…They find it hard to visualize the architecture of a bacterial operon or how the gene, RNA, and protein components interact with each other to regulate the operon. …”
Publicado 2023
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583por Goetz, Alexandra, Mader, Andreas, von Bronk, Benedikt, Weiss, Anna S., Opitz, Madeleine“…Here, using fluorescence time-lapse microscopy, we quantify noise dynamics in an artificial operon in Escherichia coli, which is based on the native operon of ColicinE2, a toxin. …”
Publicado 2020
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584por Henke, Nadja A., Heider, Sabine A. E., Hannibal, Silvin, Wendisch, Volker F., Peters-Wendisch, Petra“…The crtEcg0722crtBIYEb operon comprises most of its genes for terpenoid biosynthesis. …”
Publicado 2017
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585por Rajeev, Lara, Luning, Eric G., Zane, Grant M., Juba, Thomas R., Kazakov, Alexey E., Novichkov, Pavel S., Wall, Judy D., Mukhopadhyay, Aindrila“…The central carbon/lactate utilization pathway in the model sulfate-reducing bacterium, Desulfovibrio vulgaris Hildenborough, is encoded by the highly conserved operon DVU3025-3033. Our earlier in vitro genome-wide study had suggested a network of four two-component system regulators that target this large operon; however, how these four regulators control this operon was not known. …”
Publicado 2019
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586por Hu, Rouh-Mei, Liao, Sih-Ting, Huang, Chiang-Ching, Huang, Yi-Wei, Yang, Tsuey-Ching“…Overexpression of the fuaABC operon contributed to the fusaric acid resistance. …”
Publicado 2012
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587“…Sulfur metabolism is one of the oldest known environmental processes. The operon involved in this process is called the dsr operon. …”
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588por Jayaraman, Jay, Jones, William T., Harvey, Dawn, Hemara, Lauren M., McCann, Honour C., Yoon, Minsoo, Warring, Suzanne L., Fineran, Peter C., Mesarich, Carl H., Templeton, Matthew D.“…This operon is predicted to have a role in the transport, elongation and termination of the CPA oligosaccharide and is referred to as the TET operon. …”
Publicado 2020
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589por Vornhagen, Jay, Bassis, Christine M., Ramakrishnan, Srividya, Hein, Robert, Mason, Sophia, Bergman, Yehudit, Sunshine, Nicole, Fan, Yunfan, Holmes, Caitlyn L., Timp, Winston, Schatz, Michael C., Young, Vincent B., Simner, Patricia J., Bachman, Michael A.“…These plasmids displayed substantial variation in plasmid incompatibility type and gene content. Moreover, the ter operon was genetically independent of other plasmid-encoded virulence and antibiotic resistance loci, both in our original patient cohort and in a large set (n = 88) of publicly available ter operon-encoding Kp plasmids, indicating that the ter operon is likely playing a direct, but yet undescribed role in Kp disease. …”
Publicado 2021
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590por Lei, Ting, Yang, Junshu, Zheng, Li, Markowski, Todd, Witthuhn, Bruce A., Ji, Yinduo“…Moreover, we found that the depletion of Gcp did not influence the transcription level of CodY, a known repressor of the ilv-leu operon, while induced the transcription of CcpA, a known positive regulator of the ilv-leu operon. …”
Publicado 2012
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591“…The expression of various carbon metabolic genes was altered, including a PTS operon (which we here denote as the bgu operon) that has high similarity with the cel locus. …”
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592por Matsuoka, Jun-ichi, Ishizuna, Fumiko, Kurumisawa, Keigo, Morohashi, Kengo, Ogawa, Tetsuhiro, Hidaka, Makoto, Saito, Katsuharu, Ezawa, Tatsuhiro, Aono, Toshihiro“…The rebR gene in the reb operon encodes an activator. Three PraR binding sites and a RebR binding site are present in the promoter region of the reb operon. …”
Publicado 2017
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593“…Results indicate that, biocontrol ability of this isolate is attributed to gcd gene encoding glucose dehydrogenase, genes encoding its co-enzyme pyrroloquinoline quinone (PQQ), and two genes (sup5 and sup6) which seem to be organized in a putative operon. This operon (named supX) consists of five genes, one of which encodes a non-ribosomal peptide synthase. …”
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594“…In other genomes such as Pseudomonas aeruginosa the bioH gene is within a biotin synthesis operon and its transcription is coregulated with the other biotin operon genes. …”
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595por Yokoyama, Tatsuhiko, Niinae, Tomoya, Tsumagari, Kazuya, Imami, Koshi, Ishihama, Yasushi, Hizukuri, Yohei, Akiyama, Yoshinori“…Our data showed that the levels of several Fec system proteins encoded by the fecABCDE operon (fec operon) were significantly decreased in an RseP-deficient strain. …”
Publicado 2021
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596por Klee, Sara M., Sinn, Judith P., Held, Jeremy, Vosburg, Chad, Holmes, Aleah C., Lehman, Brian L., Peter, Kari A., McNellis, Timothy W.“…The data suggest that E. amylovora RfaH directly, specifically, and exclusively suppresses operon polarity in the amylovoran operon and a lipopolysaccharide operon.…”
Publicado 2022
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597por Ragunathan, Preethi T., Ng Kwan Lim, Evelyne, Ma, Xiangqian, Massé, Eric, Vanderpool, Carin K.“…While new functions of DicB and DicF have been identified in recent years, the mechanisms controlling the expression of the dicBF operon have remained unclear. Transcription from dicBp, the major promoter of the dicBF operon, is repressed by DicA. …”
Publicado 2023
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598por Sperandio, Daniel, Decoin, Victorien, Latour, Xavier, Mijouin, Lily, Hillion, Mélanie, Feuilloley, Marc G J, Orange, Nicole, Merieau, Annabelle“…Disruption of the hrpU-like operon (the basal part of type III secretion system from rhizospheric strains) suppresses this activity. …”
Publicado 2012
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599“…In Enterobacteriaceae, decreased silver susceptibility has been mapped to two homologous operons; the chromosomally located cus operon and the plasmid based sil operon. …”
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600“…The expression of several genes and operons, including the ula operon (which has been previously shown to be involved in ascorbic acid utilization), the AdcR regulon (which has been previously shown to be involved in zinc transport and virulence) and a PTS operon (which we denote here as ula2 operon) were altered in the presence of ascorbic acid. …”
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