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1241“…The Mtb genome harbors only one putative iron–sulphur cluster (ISC) operon (rv1460-66) predicted to be involved in the generation of the Fe–S cofactor. …”
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1242por Lessa, Fernanda C., Milucky, Jennifer, Rouphael, Nadine G., Bennett, Nancy M., Talbot, H. Keipp, Harrison, Lee H., Farley, Monica M., Walston, Jeremy, Pimenta, Fabiana, Gertz, Robert E., Rajam, Gowrisankar, Carvalho, Maria da Gloria, Beall, Bernard, Whitney, Cynthia G.“…Whole genome sequencing revealed three distinct S. mitis clones, each representing a cps1 operon highly similar to the pneumococcal cps1 reference operon. …”
Publicado 2018
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1243por Piechota, Małgorzata, Kot, Barbara, Frankowska-Maciejewska, Aneta, Grużewska, Agata, Woźniak-Kosek, Agnieszka“…MRSA (73) and MSSA (57) strains were evaluated for biofilm production by the microtiter plate method. The presence of ica operon was investigated by PCR. Out of 130 strains, 99.2% were biofilm producers. …”
Publicado 2018
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1244por Lemmens, Liesbeth, Tilleman, Laurentijn, De Koning, Ezra, Valegård, Karin, Lindås, Ann-Christin, Van Nieuwerburgh, Filip, Maes, Dominique, Peeters, Eveline“…The thermoacidophilic crenarchaeon Sulfolobus acidocaldarius harbors a GntR-like regulator belonging to the YtrA subfamily, encoded as the first gene in an operon with a second gene encoding a putative membrane protein. …”
Publicado 2019
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1245por Choi, Okhee, Bae, Juyoung, Kang, Byeongsam, Lee, Yeyeong, Kim, Seunghoe, Fuqua, Clay, Kim, Jinwoo“…Similarly, exogenous octopine binds to OccR, resulting in OoxR/octopine complexes that bind to the promoter of the octopine oxidase gene (oox) operon and activate the transcription of ooxB-lacZY, resulting in blue pigmentation in the presence of X-gal. …”
Publicado 2019
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1246por Kothari, Ankita, Soneja, Drishti, Tang, Albert, Carlson, Hans K., Deutschbauer, Adam M., Mukhopadhyay, Aindrila“…We experimentally validated the function of a putative mercury resistance operon present on an abundant 8-kbp native plasmid found in groundwater samples without detectable levels of mercury. …”
Publicado 2019
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1247por Garber, Jolene M., Nothaft, Harald, Pluvinage, Ben, Stahl, Martin, Bian, Xiaoming, Porfirio, Sara, Enriquez, Amber, Butcher, James, Huang, Hua, Glushka, John, Line, Eric, Gerlt, John A., Azadi, Parastoo, Stintzi, Alain, Boraston, Alisdair B., Szymanski, Christine M.“…Although the gastrointestinal pathogen Campylobacter jejuni was considered asaccharolytic, >50% of sequenced isolates possess an operon for l-fucose utilization. In C. jejuni NCTC11168, this pathway confers l-fucose chemotaxis and competitive colonization advantages in the piglet diarrhea model, but the catabolic steps remain unknown. …”
Publicado 2020
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1248por Findlay Black, Hailey, Mastromatteo, Scott, Sinha, Sunita, Ehrlich, Rachel L., Nislow, Corey, Chang Mell, Joshua, Redfield, Rosemary J.“…Here we show that one of these genes, HI0659, encodes the antitoxin of a competence-regulated toxin-antitoxin operon (‘toxTA’), likely acquired by horizontal gene transfer from a Streptococcus species. …”
Publicado 2020
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1249por Trouillon, Julian, Sentausa, Erwin, Ragno, Michel, Robert-Genthon, Mylène, Lory, Stephen, Attrée, Ina, Elsen, Sylvie“…The characterization of ErfA regulon across P. aeruginosa subfamilies revealed a second conserved target, the ergAB operon, with functions unrelated to virulence. To gain insights into this functional dichotomy, we defined the pan-regulon of ErfA in several Pseudomonas species and found ergAB as the sole conserved target of ErfA. …”
Publicado 2020
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1250por Zhao, Ming-Min, Lyu, Ning, Wang, Dong, Wu, Xiao-Gang, Zhao, Yuan-Zheng, Zhang, Li-Qun, Zhou, Hong-You“…Biosynthesis of 2,4-DAPG is controlled by regulating expression of the phlACBD operon at the post-transcriptional level. The phlG gene is located between the phlF and phlH genes, upstream of the phlACBD biosynthetic operon. …”
Publicado 2020
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1251por Guan, Qingtian, Ummels, Roy, Ben-Rached, Fathia, Alzahid, Yara, Amini, Mohammad S., Adroub, Sabir A., van Ingen, Jakko, Bitter, Wilbert, Abdallah, Abdallah M., Pain, Arnab“…Furthermore, we identified the exclusive presence of the espACD operon in M. kansasii subtype I, and we confirmed its role in the pathogenicity of M. kansasii in a cell infection model. …”
Publicado 2020
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1252Prophage encoding toxin/antitoxin system PfiT/PfiA inhibits Pf4 production in Pseudomonas aeruginosapor Li, Yangmei, Liu, Xiaoxiao, Tang, Kaihao, Wang, Weiquan, Guo, Yunxue, Wang, Xiaoxue“…The PfiT toxin directly binds to PfiA and functions as a corepressor of PfiA for the TA operon. The PfiAT complex exhibited autoregulation by binding to a palindrome (5′‐AATTCN(5) GTTAA‐3′) overlapping the ‐35 region of the TA operon. …”
Publicado 2020
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1253por Tang, Dong-Jie, Du, Xinyu, Shi, Qiang, Zhang, Jian-Ling, He, Yuan-Ping, Chen, Yan-Miao, Ming, Zhenhua, Wang, Dan, Zhong, Wan-Ying, Liang, Yu-Wei, Liu, Jin-Yang, Huang, Jian-Ming, Zhong, Yun-Shi, An, Shi-Qi, Gu, Hongzhou, Tang, Ji-Liang“…Here, we characterize a SAM-I riboswitch (SAM-I(Xcc)) from the Xanthomonas campestris that regulates methionine synthesis via the met operon. In vitro and in vivo experiments show that SAM-I(Xcc) controls the met operon primarily at the translational level in response to cellular S-adenosylmethionine (SAM) levels. …”
Publicado 2020
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1254por Walsh, Brenna J. C., Wang, Jiefei, Edmonds, Katherine A., Palmer, Lauren D., Zhang, Yixiang, Trinidad, Jonathan C., Skaar, Eric P., Giedroc, David P.“…The addition of exogenous inorganic sulfide reveals that A. baumannii encodes two persulfide-sensing transcriptional regulators, a primary σ(54)-dependent transcriptional activator (FisR), and a secondary system controlled by the persulfide-sensing biofilm growth-associated repressor (BigR), which is only induced by sulfide in a fisR deletion strain. FisR activates an operon encoding a sulfide oxidation/detoxification system similar to that characterized previously in Staphylococcus aureus, while BigR regulates a secondary persulfide dioxygenase (PDO2) as part of yeeE-yedE-pdo2 sulfur detoxification operon, found previously in Serratia spp. …”
Publicado 2020
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1255por Revilla-Guarinos, Ainhoa, Dürr, Franziska, Popp, Philipp F., Döring, Maximilian, Mascher, Thorsten“…Global transcriptional profiling identified a very narrow and specific response, primarily resulting in strong upregulation of the lnrLMN operon, encoding an ABC transporter previously associated with linearmycin resistance. …”
Publicado 2020
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1256por Kushwaha, Simran Krishnakant, Bhavesh, Narra Lakshmi Sai, Abdella, Bahaa, Lahiri, Chandrajit, Marathe, Sandhya Amol“…The strains differed in their CRISPR1-leader and cas operon features assorting into two main clades, CRISPR1-STY/cas-STY and CRISPR1-STM/cas-STM, comprising majorly typhoidal and non-typhoidal Salmonella serovars respectively. …”
Publicado 2020
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1257“…Here, we find that E. tracheiphila has horizontally acquired an operon with a microbial expansin (exlx) gene adjacent to a glycoside hydrolase family 5 (gh5) gene. …”
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1258“…That is, gene expression noise causes the population before the switch to divide into subpopulations with zero and nonzero lac operon expression. While “sensorless” cells with zero preexisting lac expression at the switch have long lags because they are unable to sense the lactose signal, any nonzero lac operon expression suffices to ensure a short lag. …”
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1259por Walter, Tatjana, Veldmann, Kareen H., Götker, Susanne, Busche, Tobias, Rückert, Christian, Kashkooli, Arman Beyraghdar, Paulus, Jannik, Cankar, Katarina, Wendisch, Volker F.“…Indole, hydroquinone, and 1,2,4-trihydroxybenzene may function as inducers of the iolT2-rhcM2D2 operon in vivo as they interfered with DNA binding of Cg3388 at physiological concentrations in vitro. …”
Publicado 2020
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1260por Cuenca-Arias, Paloma, Montaño, Lucy Angeline, Villarreal, José Miguel, Wiesner, Magdalena“…Most of the monophasic Salmonella Typhimurium variants that have circulated in Colombia since 2015 lacked the second phase of operon fljAB, which is related to the European/Spanish clone. …”
Publicado 2020
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