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1441por Yu, Jun Myoung, Wang, Dongping, Ries, Tessa R., Pierson, Leland S., Pierson, Elizabeth A.“…The expression of the P. chlororaphis 30–84 phenazine biosynthetic operon (phzXYFABCD) is dependent on the PhzR/PhzI quorum sensing system located immediately upstream of the biosynthetic operon as well as other regulatory systems including Gac/Rsm. …”
Publicado 2018
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1442por Gómez-Mejia, Alejandro, Gámez, Gustavo, Hirschmann, Stephanie, Kluger, Viktor, Rath, Hermann, Böhm, Sebastian, Voss, Franziska, Kakar, Niamatullah, Petruschka, Lothar, Völker, Uwe, Brückner, Reinhold, Mäder, Ulrike, Hammerschmidt, Sven“…Striking examples are genes for fatty acid biosynthesis, genes of the arginine deiminase system, and the psa operon encoding the manganese ABC transport system. …”
Publicado 2018
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1443por Mobbs, Charles V.“…A key observation is that, as with the lac operon, glucose induces genes that promote glycolysis and inhibits gene expression of alternative metabolic pathways including the pentose pathway, beta oxidation, and the TCA cycle. …”
Publicado 2018
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1444por Noguchi, Yuji, Kashiwagi, Norimasa, Uzura, Atsuko, Ogino, Chiaki, Kondo, Akihiko, Ikeda, Haruo, Sota, Masahiro“…Xylose isomerase (xylA) promoter derived from xylose (xyl) operon was selected due to strong expression of xylose isomerase (XylA) in the presence of d-xylose. …”
Publicado 2018
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1445por Wang, Tianshu, Zhao, Xiyun, Shi, Haowen, Sun, Li, Li, Yongbin, Li, Qin, Zhang, Haowei, Chen, Sanfeng, Li, Jilun“…In this study, we for the first time reveal that GlnR of Paenibacillus polymyxa WLY78 is essentially required for nif gene transcription under nitrogen limitation, whereas both GlnR and glutamine synthetase (GS) encoded by glnA within glnRA operon are required for repressing nif expression under excess nitrogen. …”
Publicado 2018
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1446por Barroso, Kelly C. M., Previato-Mello, Maristela, Batista, Bianca B., Batista, Juliana H., da Silva Neto, José F.“…Using DNA microarray, Northern blot and EMSA assays, we demonstrated that EmrR represses directly a few dozen genes, including the emrCAB operon and other genes related to transport, oxidative stress and virulence. …”
Publicado 2018
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1447por Kandari, Divya, Gopalani, Monisha, Gupta, Manish, Joshi, Hemant, Bhatnagar, Sonika, Bhatnagar, Rakesh“…The DNA binding capability of the purified BaZur to the upstream regions of the ba zur operon, yciC, rpmG, znuA, and genes encoding a GTPase cobalamine synthesis protein and a permease was ascertained by electrophoretic mobility shift assays. …”
Publicado 2019
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1448por Dang, Yulei, Zhao, Fengjie, Liu, Xiangsheng, Fan, Xu, Huang, Rui, Gao, Weixia, Wang, Shufang, Yang, Chao“…Nevertheless, iturin A could not be synthesized by strain LL3, possibly resulting from low transcription level of the itu operon. RESULTS: In this work, enhanced transcription of the iturin A biosynthetic genes was implemented by inserting a strong constitutive promoter C2up into upstream of the itu operon, leading to the production of iturin A with a titer of 37.35 mg l(−1). …”
Publicado 2019
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1449por Zhuge, Xiangkai, Sun, Yu, Jiang, Min, Wang, Juanfang, Tang, Fang, Xue, Feng, Ren, Jianluan, Zhu, Weiyun, Dai, Jianjun“…In this study, we identified that APEC acs-yjcH-actP operon, encoding acetate assimilation system, presented the host-induced transcription during its proliferation in macrophages. …”
Publicado 2019
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1450“…It has been shown that acetylated CshA positively regulates expression of ylxR-containing operon. Here, we report additional mutations in yqfO or tsaD required for the GI of sigX. …”
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1451por Gao, Qianqian, Meng, Xiaobin, Gu, Hanfu, Chen, Xueqin, Yang, Huaqing, Qiao, Yangyang, Guo, Xuemin“…ISAba1 was found to insert into the intergenic region between the csu operon and the acrR gene and should be responsible for the significant up-regulation of acrR, which was proposed to be associated with biofilm formation. …”
Publicado 2019
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1452“…We note that expression of aureolysin is largely repressed by these factors, while the spl operon is subject to the strongest upregulation of any protease loci, particularly by SarR and SaeR. …”
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1453por Miller, Robert J., Crosby, Heidi A., Schilcher, Katrin, Wang, Yu, Ortines, Roger V., Mazhar, Momina, Dikeman, Dustin A., Pinsker, Bret L., Brown, Isabelle D., Joyce, Daniel P., Zhang, Jeffrey, Archer, Nathan K., Liu, Haiyun, Alphonse, Martin P., Czupryna, Julie, Anderson, William R., Bernthal, Nicholas M., Fortuno-Miranda, Lea, Bulte, Jeff W. M., Francis, Kevin P., Horswill, Alexander R., Miller, Lloyd S.“…In vivo bioluminescence imaging has been used to monitor Staphylococcus aureus infections in preclinical models by employing bacterial reporter strains possessing a modified lux operon from Photorhabdus luminescens. However, the relatively short emission wavelength of lux (peak 490 nm) has limited tissue penetration. …”
Publicado 2019
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1454por Oshlag, J. Zachary, Ma, Yanjun, Morse, Kaitlin, Burger, Brian T., Lemke, Rachelle A., Karlen, Steven D., Myers, Kevin S., Donohue, Timothy J., Noguera, Daniel R.“…Comparative gene expression analyses of SA008.1.07 implicated the involvement of products of the vanARB operon (rpa3619, rpa3620, rpa3621), which has been described as catalyzing aerobic aromatic ring demethylation in other bacteria, in anaerobic syringic acid degradation. …”
Publicado 2020
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1455por Kamminga, Tjerko, Benis, Nirupama, Martins dos Santos, Vitor, Bijlsma, Jetta J. E., Schaap, Peter J.“…Six out of seven genes in the operon encoding the mycoplasma specific F1-like ATPase (MHP_RS02445-MHP_RS02475) and all genes in the operon MHP_RS01965-MHP_RS01990 with functions related to nucleotide metabolism, spermidine transport and glycerol-3-phoshate transport were up-regulated in vivo. …”
Publicado 2020
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1456por Kosecka-Strojek, Maja, Sadowy, Ewa, Gawryszewska, Iwona, Klepacka, Joanna, Tomasik, Tomasz, Michalik, Michal, Hryniewicz, Waleria, Miedzobrodzki, Jacek“…Isolates were characterized phenotypically by determining their antimicrobial resistance patterns and using molecular methods such as PFGE, MLST, SCCmec typing, detection of the ica operon, and analysis of antimicrobial resistance determinants. …”
Publicado 2020
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1457por Campelo, Ana Belén, López-González, María Jesús, Escobedo, Susana, Janzen, Thomas, Neves, Ana Rute, Rodríguez, Ana, Martínez, Beatriz“…Moreover, P(ysaD) promoter fusions, designed to measure the activation of the detoxification module, revealed that the ysaB mutations unlock transcriptional control by TCS-G, resulting in constitutive expression of the ysaDCB operon. Finally, deletion of ysaD was also performed to get an insight into the function of this gene. ysaD encodes a secreted peptide and is part of the ysaDCB operon. …”
Publicado 2020
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1458por Soutourina, Olga, Dubois, Thomas, Monot, Marc, Shelyakin, Pavel V., Saujet, Laure, Boudry, Pierre, Gelfand, Mikhail S., Dupuy, Bruno, Martin-Verstraete, Isabelle“…We present here the first transcriptional map of the C. difficile genome resulting from the identification of transcriptional start sites (TSS), promoter motifs and operon structures. By 5′-end RNA-seq approach, we mapped more than 1000 TSS upstream of genes. …”
Publicado 2020
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1459por Kelwick, Richard, Ricci, Luca, Chee, Soo Mei, Bell, David, Webb, Alexander J, Freemont, Paul S“…In cell-free transcription–translation prototyping reactions, gas chromatography–mass spectrometry quantification of cell-free 3-hydroxybutyrate (3HB) production revealed differences between the activities of the Native ΔPhaC_C319A (1.18 ± 0.39 µM), C104 ΔPhaC_C319A (4.62 ± 1.31 µM) and C101 ΔPhaC_C319A (2.65 ± 1.27 µM) phaCAB operons that were tested. Interestingly, the most active operon, C104 produced higher levels of PHAs (or PHAs monomers) than the Native phaCAB operon in both in vitro and in vivo assays. …”
Publicado 2018
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1460Detection and Control of Biofilm Formation by Staphylococcus aureus from Febrile Neutropenic Patient“…The icaA and icaD genes were present in only 50% of biofilm-productive bacteria. CONCLUSION: The ica operon is present in only 50% of biofilm-productive S. aureus and Linezolid is the best antibiotic against these bacteria.…”
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