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901“…Among these, expression of the groESL operon was induced by more than fourfold and was consequently selected to improve C. beijerinckii tolerance to ferulic acid. …”
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902“…Furthermore, the TSSs, TTSs, operons, promoters and unstranslated regions that we have defined for S. …”
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903Genetic import and phenotype specific alleles associated with hyper-invasion in Campylobacter jejunipor Baig, Abiyad, McNally, Alan, Dunn, Steven, Paszkiewicz, Konrad H., Corander, Jukka, Manning, Georgina“…A novel cytolethal distending toxin (cdt) operon was also identified as present in all hyper-invasive strains in addition to the classic cdt operon present in other C. jejuni. …”
Publicado 2015
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904por García, Patricia, Malorny, Burkhard, Rodicio, M. Rosario, Stephan, Roger, Hächler, Herbert, Guerra, Beatriz, Lucarelli, Claudia“…Typhimurium incapable of expressing the second-phase flagellar antigen (fljAB operon), and it is recognized to be one of the most prevalent serovars causing human infections. …”
Publicado 2016
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905por Gupta, Manish, Nayyar, Nishtha, Chawla, Meenakshi, Sitaraman, Ramakrishnan, Bhatnagar, Rakesh, Banerjee, Nirupama“…We have investigated the parDE2 operon of M. tuberculosis H37Rv encoding MParE2 toxin and MParD2 antitoxin proteins. …”
Publicado 2016
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906“…The genes encoding a two-component regulator (PnpRS) are located immediately upstream of the pst1 operon. Both the pst1 and pst2 operons encode putative PhoU-family regulators (PhoU1 and PhoU2) at their ends. …”
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907“…The results support that SmeSy-SmeRy TCS is responsible for the regulation of smeYZ operon; whereas SmeSy may be cognate with another unidentified response regulator for the regulation of smeDEF operon. …”
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908por Weissenbach, Julia, Ilhan, Judith, Bogumil, David, Hülter, Nils, Stucken, Karina, Dagan, Tal“…The genome of C. fritschii encodes two groES/groEL operons (groESL1, groESL1.2) and a monocistronic groEL gene (groEL2). …”
Publicado 2017
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909“…The minor pilins and PilY1 are encoded in an operon that is positively regulated by the FimS-AlgR two-component system. …”
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910“…The native producer Pseudomonas aeruginosa harbors two identically structured operons in its genome, which encode the enzymes responsible for PCA synthesis [phzA1-G1 (operon 1), phzA2-G2 (operon 2)]. …”
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911por Bradshaw, Michael, Grewe, Felix, Thomas, Anne, Harrison, Cody H., Lindgren, Hanna, Muggia, Lucia, St. Clair, Larry L., Lumbsch, H. Thorsten, Leavitt, Steven D.“…BACKGROUND: Regions within the nuclear ribosomal operon are a major tool for inferring evolutionary relationships and investigating diversity in fungi. …”
Publicado 2020
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912por Nagar, Shekhar, Talwar, Chandni, Haider, Shazia, Puri, Akshita, Ponnusamy, Kalaiarasan, Gupta, Madhuri, Sood, Utkarsh, Bajaj, Abhay, Lal, Rup, Kumar, Roshan“…We also determined the complete Bacteroides aerotolerance (Bat) operon (batA, batB, batC, batD, batE, hypothetical protein, moxR, and pa3071) within the genome of Parapedobacter indicus RK1(T). …”
Publicado 2020
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913por Driscoll, Timothy P., Verhoeve, Victoria I., Brockway, Cassia, Shrewsberry, Darin L., Plumer, Mariah, Sevdalis, Spiridon E., Beckmann, John F., Krueger, Laura M., Macaluso, Kevin R., Azad, Abdu F., Gillespie, Joseph J.“…Alternately, wCfeJ harbors a toxin-antidote operon analogous to the wPip cinAB operon recently characterized as an inducer of cytoplasmic incompatibility (CI) in flies. wCfeJ cinB and three adjacent genes are collectively similar to large modular toxins encoded in CI-like operons of certain Wolbachia strains and Rickettsia species, signifying that CI toxins streamline by fission of large modular toxins. …”
Publicado 2020
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914por Wagner, Theresa Maria, Janice, Jessin, Sivertsen, Audun, Sjögren, Ingegerd, Sundsfjord, Arnfinn, Hegstad, Kristin“…In VVESwe-R the vanHAX-operon is constitutively expressed at a level comparable to the non-induced prototype E. faecium BM4147 strain. …”
Publicado 2020
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915“…Only 15.3% of isolates (SE) were positive for both the icaAD and the ica operon. Phenotypically, 19.2% of SE isolates were strong biofilm producers, among which three were both icaAD- and ica operon-positive. …”
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916por Katani, Robab, Kudva, Indira T., Srinivasan, Sreenidhi, Stasko, Judith B., Schilling, Megan, Li, Lingling, Cote, Rebecca, DebRoy, Chitrita, Arthur, Terrance M., Sokurenko, Evgeni V., Kapur, Vivek“…Super-shed (SS) Escherichia coli O157 (E. coli O157) demonstrate a strong, aggregative, locus of enterocyte effacement (LEE)-independent adherence phenotype on bovine recto-anal junction squamous epithelial (RSE) cells, and harbor polymorphisms in non-LEE-adherence-related loci, including in the type 1 fimbriae operon. To elucidate the role of type 1 fimbriae in strain- and host-specific adherence, we evaluated the entire Fim operon (FimB-H) and its adhesion (FimH) deletion mutants in four E. coli O157 strains, SS17, SS52, SS77 and EDL933, and evaluated the adherence phenotype in bovine RSE and human HEp-2 adherence assays. …”
Publicado 2021
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917“…It possessed highly conserved RNA I/II and Tn602 (IS903-aph-IS903) regions to two other KanR plasmids pSe-Kan and pSBardo-Kan, but carried a mobC-mobA/BD operon. The mobilization proteins encoded by the mob operon of pSNC3-Kan showed high sequence identity (~95%) to those of an E. coli plasmid pEC34B, except that MobE was not present; and were much less conserved to those of another KanR plasmid pSN11/00Kan (43% - 86% identity). …”
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918por Conway, Jonathan M., Walton, William G., Salas-González, Isai, Law, Theresa F., Lindberg, Chloe A., Crook, Laura E., Kosina, Suzanne M., Fitzpatrick, Connor R., Lietzan, Adam D., Northen, Trent R., Jones, Corbin D., Finkel, Omri M., Redinbo, Matthew R., Dangl, Jeffery L.“…We determine the crystal structures and binding properties of the operon’s MarR-family repressor with IAA and other auxins. …”
Publicado 2022
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919por Frenkel, Alona, Zecharia, Eli, Gómez-Pérez, Daniel, Sendersky, Eleonora, Yegorov, Yevgeni, Jacob, Avi, Benichou, Jennifer I. C., Stierhof, York-Dieter, Parnasa, Rami, Golden, Susan S., Kemen, Eric, Schwarz, Rakefet“…Detailed characterization of EbfG4 encoded by this operon revealed cell-surface localization as well as its presence in the biofilm matrix. …”
Publicado 2023
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920por Zhang, Yang, Zhou, Xiuling, Wang, Xuemei, Wang, Lu, Xia, Menglei, Luo, Jianmei, Shen, Yanbing, Wang, Min“…RESULTS: There is a complete MCC in Mycobacterium neoaurum (MNR), prpC, prpD and prpB in the prp operon encode methylcitrate synthase, methylcitrate dehydratase and methylisocitrate lyase involved in MCC, and PrpR is a specific transcriptional activator of prp operon. …”
Publicado 2020
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