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1701por Bolt, Edward L., Jenkins, Tabitha, Russo, Valeria Moreira, Ahmed, Sharlene, Cavey, James, Cass, Simon D.“…RpmG is frequently annotated as a bacterial ribosomal protein, although forms an operon with MutM glycosylase and a putative deubiquitinating (DUB) enzyme, YicR. …”
Publicado 2016
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1702por Gomes, Jaqueline Conceição Meireles, Azevedo, Juliana Simão Nina de, Veras, Adonney Allan de Oliveira, Alves, Jorianne Thyeska Castro, Henriques, Isabel, Correia, António, Silva, Artur Luiz da Costa da, Carneiro, Adriana Ribeiro“…The genome has a G + C content of 42.7%, 2618 open reading frames (ORFs), three copies of the rRNAs operon, and 29 tRNA genes. Twenty-five sequences related to the degradation of aromatic compounds were predicted, as well as numerous genes related to resistance to metals or metal(loid)s. …”
Publicado 2016
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1703por Asiani, Karishma R., Williams, Huw, Bird, Louise, Jenner, Matthew, Searle, Mark S., Hobman, Jon L., Scott, David J., Soultanas, Panos“…The putative model of Ag(+) resistance, encoded by the sil operon from pMG101, involves export of Ag(+) via an ATPase (SilP), an effluxer complex (SilCFBA) and a periplasmic chaperon of Ag(+) (SilE). …”
Publicado 2016
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1704por Heinrich, Antje K., Glaeser, Angela, Tobias, Nicholas J., Heermann, Ralf, Bode, Helge B.“…We identified a novel type of transcriptional regulator, AntJ, which activates expression of the antA-I operon responsible for AQ production. AntJ heterogeneously activates the AQ production in single P. luminescens 1° cells, and blocks AQ production in 2° cells. …”
Publicado 2016
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1705“…We identified the per operon as the key component of the hysteretic switch. …”
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1706“…In some pathogenic bacteria, an operon‐encoded mono‐ADP‐ribosylation cycle mediates response to host‐induced oxidative stress. …”
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1707por Quigley, Jeff, Hughitt, V. Keith, Velikovsky, Carlos A., Mariuzza, Roy A., El-Sayed, Najib M., Briken, Volker“…We characterized the DNA interaction and the regulon of Rv3167c, a transcriptional repressor that is involved in virulence regulation of M. tuberculosis, and discovered that it controls the PDIM operon. A loss-of-function genetic approach showed that PDIM levels directly correlate with the capacity of M. tuberculosis to escape the phagosome and induce host cell necrosis and macroautophagy. …”
Publicado 2017
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1708“…In our study published in MBio [Joo et al., 7(5). pii: e01579-16], we show that phenol-soluble modulins (PSMs), important peptide toxins of S. aureus, release a repressor from the promoter of the operon encoding the toxin export system, thereby enabling toxin secretion. …”
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1709“…We highlight how these studies have brought novel concepts in prokaryotic gene regulation, such as the ‘excludon’ where the 5′-UTR of a messenger also acts as an antisense regulator of an operon transcribed in opposite orientation, or the notion that riboswitches can regulate non-coding RNAs to integrate complex metabolic stimuli into regulatory networks. …”
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1710por Pando, Jasmine M., Karlinsey, Joyce E., Lara, Jimmie C., Libby, Stephen J., Fang, Ferric C.“…Nineteen genes activated by the RcsA-RcsB response regulator make up an operon responsible for the production of colanic acid capsular polysaccharide, which promotes biofilm development. …”
Publicado 2017
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1711“…We also find that in B. subtilis, the glycine riboswitch-regulated gcvT operon is important for glycine detoxification.…”
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1712“…Among the upregulated genes, a signal transduction response regulator (ArsR) and a signal transduction histidine kinase (SthK) were predicted to be located on the same operon. A mutant was constructed by deletion of both of these genes. …”
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1713“…We achieved the regulation of protein expression in the cell-mimic particles by the usage of lac operon. The cell-mimic particles quickly responded to the concentration change of isopropyl β-d-1-thiogalactopyranoside (IPTG) in the feeding buffer to regulate the mCherry expression level. …”
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1714“…The method was used to isolate promoter DNA binding proteins, which bind and regulate the dsz operon in Gordonia sp. IITR 100 responsible for biodesulfurization of organosulfurs. …”
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1715“…The latter relieved repression of the badDEFGAB operon by binding to BadM, triggering the synthesis of enzymes that activate and dearomatize the benzene ring. …”
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1716por Arnold, Jason W., Simpson, Joshua B., Roach, Jeffery, Bruno-Barcena, Jose M., Azcarate-Peril, M. Andrea“…Physiological and transcriptomics analyses showed distinct differences in carbohydrate metabolism profiles and GOS utilization between strains. A putative operon responsible for GOS utilization was identified and characterized by genetic disruption of the 6-phospho-β-galactosidase, which had a critical role in GOS utilization. …”
Publicado 2018
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1717“…Here, based on a bioinformatic analysis of cyanobacterial oxygen evolution and reduction enzymes (photosystem II: PS II and cytochrome c oxidase: COX, respectively), the gene encoding the catalytic D1 subunit of PS II was found to be expressed individually across 38 phylogenetically diverse strains, which is in contrast to the operon structure of the genes encoding major COX subunits. …”
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1718“…Many pAgos are associated with putative nucleases, helicases, and DNA binding proteins in the same gene or operon, suggesting that they are involved in target processing. …”
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1719“…The putative virulence determinants include 11 genes associated with the virulence operon associated with protein synthesis or DNA transcription and ten genes with antibiotic and toxic compound resistance. …”
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1720por Milyutina, Irina A., Belevich, Tatyana A., Ilyash, Lyudmila V., Troitsky, Aleksey V.“…Partial sequence of a ribosomal operon (the 5,298 bp includes partial 18S and 28S rDNA, complete 5.8S rDNA, ITS1, and ITS2 sequences) and a partial 2,112 bp chloroplast 23S rDNA sequence White Sea Pedinophyceae was amplified from metagenomic DNA by specific primers and sequenced. …”
Publicado 2019
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