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781por Hurtado-Escobar, Genaro Alejandro, Grépinet, Olivier, Raymond, Pierre, Abed, Nadia, Velge, Philippe, Virlogeux-Payant, Isabelle“…We demonstrated that the nucleoid-associated proteins H-NS and Hha, and their respective paralogs StpA and YdgT, negatively regulate at pH 5.1 and pH 7.1 the transcription of the pef operon. Two promoters, PpefB and PpefA, direct the transcription of this operon. …”
Publicado 2019
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782“…In this study, molecular biological analyses revealed the roles of three transcriptional regulators BrpR, BrpT, and BrpS in the regulatory pathway for the cabABC operon. BrpR induces brpT and BrpT in turn activates the cabABC operon in a sequential cascade, contributing to development of robust biofilm structures. …”
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783por Lee, Terence, Pang, Stanley, Stegger, Marc, Sahibzada, Shafi, Abraham, Sam, Daley, Denise, Coombs, Geoffrey“…One cluster harboured mostly non-CC17 isolates while two clusters were dominant for the vanA and vanB operons. CONCLUSION: The gradual increase in dominance of the respective van operon was observed in both the vanA and vanB dominant clusters suggesting a strain-van operon affinity. …”
Publicado 2020
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784“…Here, we show that, contrary to the case in other Gammaproteobacteria, FruR acts as a transcriptional activator of the fru operon and is indispensable for the growth of Vibrio cholerae on fructose. …”
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785por Carzaniga, Thomas, Falchi, Federica A., Forti, Francesca, Antoniani, Davide, Landini, Paolo, Briani, Federica“…Escherichia coli C is a strong biofilm producer in comparison to E. coli K-12 laboratory strains due to higher expression of the pgaABCD operon encoding the enzymes for the biosynthesis of the extracellular polysaccharide poly-β-1,6-N-acetylglucosamine (PNAG). …”
Publicado 2021
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786por Ghaioumy, Rasoul, Tabatabaeifar, Fatemehalsadat, Mozafarinia, Karamat, Mianroodi, Aliasghar Arabi, Isaei, Elham, Morones-Ramírez, José Rubén, Afshari, Setareh Agha Kuchak, Kalantar-Neyestanaki, Davood“…Molecular study of ica operon revealed that 2 (6.3%) and 19 (59.4%) isolates carried icaA and icaD, respectively. …”
Publicado 2021
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787por Santos, Ingrid Nayara Marcelino, Kurihara, Mariana Neri Lucas, Santos, Fernanda Fernandes, Valiatti, Tiago Barcelos, da Silva, Juliana Thalita Paulino, Pignatari, Antônio Carlos Campos, Salles, Mauro José“…S. haemolitycus (isolate 95), and S. lugdunensis were unable to form biofilm and did not harbor the complete icaADBCR operon. High variability of adhesion genes was detected, with atl, ebp, icaADBC operon, and IS256 being the most common. …”
Publicado 2022
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788por Chiu, Yi‐Fang, Fu, Han‐Yi, Skotnicová, Petra, Lin, Keng‐Min, Komenda, Josef, Chu, Hsiu‐An“…Whole‐genome sequencing revealed that all of these autotrophic transformants carried a variable number of tandem repeats (from 5 to 15) of chromosomal segments containing the psbEFLJ operon. RNA‐seq analysis showed greatly increased transcript levels of the psbEFLJ operon in these autotrophic transformants. …”
Publicado 2021
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789“…Analysis of the nucleotide sequence for the isophthalate degradation operon located genes for a dioxygenase, a transport protein, a cis-dihydrodiol dehydrogenase, and a reductase. …”
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790por McManus, Brenda A., O'Connor, Aoife M., Kinnevey, Peter M., O'Sullivan, Michael, Polyzois, Ioannis, Coleman, David C.“…The type III arginine catabolic mobile element (ACME) was detected in three Staphylococcus epidermidis oral isolates recovered from separate patients (one healthy, one healthy with dental implants, and one with periodontal disease) based on ACME-arc-operon- and ACME-opp3-operon-directed PCR. These isolates were subjected to whole-genome sequencing to characterize the precise structural organization of ACME III for the first time, which also revealed that all three isolates were the same sequence type, ST329.…”
Publicado 2017
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791por Petrone, Joseph R., Rios Glusberger, Paula, George, Christian D., Milletich, Patricia L., Ahrens, Angelica P., Roesch, Luiz Fernando Wurdig, Triplett, Eric W.“…Sequencing the near-entire rrn operon of bacteria and archaea enables the use of the universally conserved operon holding evolutionary polymorphisms for taxonomic resolution. …”
Publicado 2023
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792“…As a result, we identified new regulon members, functioning in respiration, central metabolism (glycolysis, gluconeogenesis, pentose phosphate pathway, citrate cicle, metabolism of pyruvate and lactate), metabolism of carbohydrates and fatty acids, transcriptional regulation and transport, in particular: the ATP synthase operon atpIBEFHAGCD, Na(+)-exporting NADH dehydrogenase operon nqrABCDEF, the D-amino acids dehydrogenase operon dadAX. …”
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793“…AO22 contains a functional mer operon with all four essential genes (merRTPA) and shows >99% DNA sequence identity to that of Tn501. …”
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794“…Furthermore, the P1 promoter of the sae operon, one of the targets of the SaeRS TCS, showed normal transcription activity. …”
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795por Huvet, M., Toni, T., Sheng, X., Thorne, T., Jovanovic, G., Engl, C., Buck, M., Pinney, J.W., Stumpf, M.P.H.“…The organization of this operon allows for surprising levels of additional transcriptional control and flexibility. …”
Publicado 2011
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796por Ohneck, Elizabeth A., Zalucki, Yaramah M., Johnson, Paul J. T., Dhulipala, Vijaya, Golparian, Daniel, Unemo, Magnus, Jerse, Ann E., Shafer, William M.“…Frequently in gonococcal strains, the expression of the mtrCDE operon is differentially regulated by both a repressor, MtrR, and an activator, MtrA. …”
Publicado 2011
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797“…In particular, in A. marginale Tat functionality is conserved despite operon splitting as a consequence of genome rearrangements. …”
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798“…Comparative analysis at nucleotide and protein levels suggest that a number of important phage related functions are missing in the e14 genome including parts of the early left operon, early right operon and late operon. The loss of these genes is the result of at least three major deletions that have occurred on e14 since its integration. …”
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799por Wang, Yun, Chen, Yin, Zhou, Qian, Huang, Shi, Ning, Kang, Xu, Jian, Kalin, Robert M., Rolfe, Stephen, Huang, Wei E.“…Pyrosequencing analysis showed that the nag2 operon was the key functional operon in naphthalene degradation in-situ, and shared homology with both nag operons in Ralstonia sp. …”
Publicado 2012
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800“…However, this 4-gene operon is only present in some Campylobacter isolates and other arsenic resistance mechanisms in C. jejuni have not been characterized. …”
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