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Sulfate and thiosulfate transport in Escherichia coli K-12: nucleotide sequence and expression of the cysTWAM gene cluster

k-12

Sirko A.
GSID: VF53fKiTTnUJ
A Sirko, M Hryniewicz, D Hulanicka… - Journal of Bacteriology, 1990 - Am Soc Microbiol

… Sulfate and thiosulfate transport in Escherichia coli K-12: identification of a gene encoding a novel protein involved in thiosulfate binding. J. Bacteriol. … Nucleotide sequence of the ugp genes of Escherichia coli K-12: homology to the maltose system....

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Sirko, A., Hryniewicz, M., Hulanicka, D., & Böck, A. (1990). Sulfate and thiosulfate transport in Escherichia coli K-12: nucleotide sequence and expression of the cysTWAM gene cluster. Journal of Bacteriology, 172(6), 3351-3357.
Sirko, Agnieszka, et al. "Sulfate and thiosulfate transport in Escherichia coli K-12: nucleotide sequence and expression of the cysTWAM gene cluster." Journal of Bacteriology 172.6 (1990): 3351-3357.
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Corrigendum: Diverse chemotypes disrupt ion homeostasis in the malaria parasite.

Molecular microbiology

[No authors listed]
PMID: 26108547
Mol Microbiol. 2015 Jul;97(1):179. doi: 10.1111/mmi.13080.

No abstract available.

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Corrigendum: Diverse chemotypes disrupt ion homeostasis in the malaria parasite. Mol Microbiol. 2015;97(1):179doi: 10.1111/mmi.13080.
(2015). Corrigendum: Diverse chemotypes disrupt ion homeostasis in the malaria parasite. Molecular microbiology, 97(1), 179. https://doi.org/10.1111/mmi.13080
"Corrigendum: Diverse chemotypes disrupt ion homeostasis in the malaria parasite." Molecular microbiology vol. 97,1 (2015): 179. doi: https://doi.org/10.1111/mmi.13080
Corrigendum: Diverse chemotypes disrupt ion homeostasis in the malaria parasite. Mol Microbiol. 2015 Jul;97(1):179. doi: 10.1111/mmi.13080. PMID: 26108547.
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A Caulobacter MreB mutant with irregular cell shape exhibits compensatory widening to maintain a preferred surface area to volume ratio.

Molecular microbiology

Harris LK, Dye NA, Theriot JA.
PMID: 25266768
Mol Microbiol. 2014 Sep 30; doi: 10.1111/mmi.12811. Epub 2014 Sep 30.

Rod-shaped bacteria typically elongate at a uniform width. To investigate the genetic and physiological determinants involved in this process, we studied a mutation in the morphogenetic protein MreB in Caulobacter crescentus that gives rise to cells with a variable-width...

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Harris LK, Dye NA, Theriot JA. A Caulobacter MreB mutant with irregular cell shape exhibits compensatory widening to maintain a preferred surface area to volume ratio. Mol Microbiol. 2014;doi: 10.1111/mmi.12811.
Harris, L. K., Dye, N. A., & Theriot, J. A. (2014). A Caulobacter MreB mutant with irregular cell shape exhibits compensatory widening to maintain a preferred surface area to volume ratio. Molecular microbiology, . https://doi.org/10.1111/mmi.12811
Harris, Leigh K, et al. "A Caulobacter MreB mutant with irregular cell shape exhibits compensatory widening to maintain a preferred surface area to volume ratio." Molecular microbiology vol. (2014). doi: https://doi.org/10.1111/mmi.12811
Harris LK, Dye NA, Theriot JA. A Caulobacter MreB mutant with irregular cell shape exhibits compensatory widening to maintain a preferred surface area to volume ratio. Mol Microbiol. 2014 Sep 30; doi: 10.1111/mmi.12811. Epub 2014 Sep 30. PMID: 25266768; PMCID: PMC4379118.
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Nucleo-cytoplasmic shuttling dynamics of the transcriptional regulators XYR1 and CRE1 under conditions of cellulase and xylanase gene expression in Trichoderma reesei.

Molecular microbiology

Lichius A, Seidl-Seiboth V, Seiboth B, Kubicek CP.
PMID: 25302561
Mol Microbiol. 2014 Oct 10; doi: 10.1111/mmi.12824. Epub 2014 Oct 10.

Trichoderma reesei is a model for investigating the regulation of (hemi-)cellulase gene expression. Cellulases are formed adaptively, and the transcriptional activator XYR1 and the carbon catabolite repressor CRE1 are main regulators of their expression. We quantified the nucleo-cytoplasmic shuttling...

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Lichius A, Seidl-Seiboth V, Seiboth B, et al. Nucleo-cytoplasmic shuttling dynamics of the transcriptional regulators XYR1 and CRE1 under conditions of cellulase and xylanase gene expression in Trichoderma reesei. Mol Microbiol. 2014;doi: 10.1111/mmi.12824.
Lichius, A., Seidl-Seiboth, V., Seiboth, B., & Kubicek, C. P. (2014). Nucleo-cytoplasmic shuttling dynamics of the transcriptional regulators XYR1 and CRE1 under conditions of cellulase and xylanase gene expression in Trichoderma reesei. Molecular microbiology, . https://doi.org/10.1111/mmi.12824
Lichius, Alexander, et al. "Nucleo-cytoplasmic shuttling dynamics of the transcriptional regulators XYR1 and CRE1 under conditions of cellulase and xylanase gene expression in Trichoderma reesei." Molecular microbiology vol. (2014). doi: https://doi.org/10.1111/mmi.12824
Lichius A, Seidl-Seiboth V, Seiboth B, Kubicek CP. Nucleo-cytoplasmic shuttling dynamics of the transcriptional regulators XYR1 and CRE1 under conditions of cellulase and xylanase gene expression in Trichoderma reesei. Mol Microbiol. 2014 Oct 10; doi: 10.1111/mmi.12824. Epub 2014 Oct 10. PMID: 25302561; PMCID: PMC4282317.
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MrpC, a CRP/Fnr homolog, functions as a negative autoregulator during the Myxococcus xanthus multicellular developmental program.

Molecular microbiology

McLaughlin PT, Bhardwaj V, Feeley BE, Higgs PI.
PMID: 29745442
Mol Microbiol. 2018 May 10; doi: 10.1111/mmi.13982. Epub 2018 May 10.

MrpC, a member of the CRP/Fnr superfamily of transcriptional regulators, plays a key role in coordination of the multicellular developmental program in Myxococcus xanthus. Previous reports suggest MrpC is subject to complex regulation including activation by an unusual LonD-dependent...

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McLaughlin PT, Bhardwaj V, Feeley BE, et al. MrpC, a CRP/Fnr homolog, functions as a negative autoregulator during the Myxococcus xanthus multicellular developmental program. Mol Microbiol. 2018;doi: 10.1111/mmi.13982.
McLaughlin, P. T., Bhardwaj, V., Feeley, B. E., & Higgs, P. I. (2018). MrpC, a CRP/Fnr homolog, functions as a negative autoregulator during the Myxococcus xanthus multicellular developmental program. Molecular microbiology, . https://doi.org/10.1111/mmi.13982
McLaughlin, Patrick T, et al. "MrpC, a CRP/Fnr homolog, functions as a negative autoregulator during the Myxococcus xanthus multicellular developmental program." Molecular microbiology vol. (2018). doi: https://doi.org/10.1111/mmi.13982
McLaughlin PT, Bhardwaj V, Feeley BE, Higgs PI. MrpC, a CRP/Fnr homolog, functions as a negative autoregulator during the Myxococcus xanthus multicellular developmental program. Mol Microbiol. 2018 May 10; doi: 10.1111/mmi.13982. Epub 2018 May 10. PMID: 29745442.
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THE AER2 RECEPTOR FROM VIBRIO CHOLERAE IS A DUAL PAS-HEME OXYGEN SENSOR.

Molecular microbiology

Greer-Phillips SE, Sukomon N, Chua TK, Johnson MS, Crane BR, Watts KJ.
PMID: 29719085
Mol Microbiol. 2018 May 02; doi: 10.1111/mmi.13978. Epub 2018 May 02.

The diarrheal pathogen Vibrio cholerae navigates complex environments using three chemosensory systems and 44-45 chemoreceptors. Chemosensory cluster II modulates chemotaxis, whereas clusters I and III have unknown functions. Ligands have been identified for only five V. cholerae chemoreceptors. Here...

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Greer-Phillips SE, Sukomon N, Chua TK, et al. THE AER2 RECEPTOR FROM VIBRIO CHOLERAE IS A DUAL PAS-HEME OXYGEN SENSOR. Mol Microbiol. 2018;doi: 10.1111/mmi.13978.
Greer-Phillips, S. E., Sukomon, N., Chua, T. K., Johnson, M. S., Crane, B. R., & Watts, K. J. (2018). THE AER2 RECEPTOR FROM VIBRIO CHOLERAE IS A DUAL PAS-HEME OXYGEN SENSOR. Molecular microbiology, . https://doi.org/10.1111/mmi.13978
Greer-Phillips, Suzanne E, et al. "THE AER2 RECEPTOR FROM VIBRIO CHOLERAE IS A DUAL PAS-HEME OXYGEN SENSOR." Molecular microbiology vol. (2018). doi: https://doi.org/10.1111/mmi.13978
Greer-Phillips SE, Sukomon N, Chua TK, Johnson MS, Crane BR, Watts KJ. THE AER2 RECEPTOR FROM VIBRIO CHOLERAE IS A DUAL PAS-HEME OXYGEN SENSOR. Mol Microbiol. 2018 May 02; doi: 10.1111/mmi.13978. Epub 2018 May 02. PMID: 29719085; PMCID: PMC6214802.
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The sigma factor σ.

Molecular microbiology

Zhang JJ, Hu WL, Yang Y, Li H, Picardeau M, Yan J, Yang XF.
PMID: 29633391
Mol Microbiol. 2018 Apr 06; doi: 10.1111/mmi.13967. Epub 2018 Apr 06.

Leptospira spp. comprise both pathogenic and free-living saprophytic species. Little is known about the environmental adaptation and survival mechanisms of Leptospira. Alternative sigma factor, σ

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Zhang JJ, Hu WL, Yang Y, et al. The sigma factor σ. Mol Microbiol. 2018;doi: 10.1111/mmi.13967.
Zhang, J. J., Hu, W. L., Yang, Y., Li, H., Picardeau, M., Yan, J., & Yang, X. F. (2018). The sigma factor σ. Molecular microbiology, . https://doi.org/10.1111/mmi.13967
Zhang, Jun-Jie, et al. "The sigma factor σ." Molecular microbiology vol. (2018). doi: https://doi.org/10.1111/mmi.13967
Zhang JJ, Hu WL, Yang Y, Li H, Picardeau M, Yan J, Yang XF. The sigma factor σ. Mol Microbiol. 2018 Apr 06; doi: 10.1111/mmi.13967. Epub 2018 Apr 06. PMID: 29633391; PMCID: PMC6174002.
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The virulence protein Yop5 of Yersinia pseudotuberculosis is regulated at transcriptional level by plasmid-plB1 -encoded trans-acting elements controlled by temperature and calcium.

Molecular microbiology

Forsberg A, Wolf-Watz H.
PMID: 28776790
Mol Microbiol. 1988 Jan;2(1):121-133. doi: 10.1111/j.1365-2958.1988.tb00013.x.

The DNA sequence of the structural gene (yopE) of one of the Yersinia pseudotuberculosis virulence plas-mid-plB1-encoded proteins, Yop5, is presented. The deduced protein showed a molecular weight of 22971 Daltons. A specific mutant, having a kanamycin-resistance fragment inserted within...

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Forsberg A, Wolf-Watz H. The virulence protein Yop5 of Yersinia pseudotuberculosis is regulated at transcriptional level by plasmid-plB1 -encoded trans-acting elements controlled by temperature and calcium. Mol Microbiol. 1988;2(1):121-133doi: 10.1111/j.1365-2958.1988.tb00013.x.
Forsberg, A., & Wolf-Watz, H. (1988). The virulence protein Yop5 of Yersinia pseudotuberculosis is regulated at transcriptional level by plasmid-plB1 -encoded trans-acting elements controlled by temperature and calcium. Molecular microbiology, 2(1), 121-133. https://doi.org/10.1111/j.1365-2958.1988.tb00013.x
Forsberg, A, and Wolf-Watz, H. "The virulence protein Yop5 of Yersinia pseudotuberculosis is regulated at transcriptional level by plasmid-plB1 -encoded trans-acting elements controlled by temperature and calcium." Molecular microbiology vol. 2,1 (1988): 121-133. doi: https://doi.org/10.1111/j.1365-2958.1988.tb00013.x
Forsberg A, Wolf-Watz H. The virulence protein Yop5 of Yersinia pseudotuberculosis is regulated at transcriptional level by plasmid-plB1 -encoded trans-acting elements controlled by temperature and calcium. Mol Microbiol. 1988 Jan;2(1):121-133. doi: 10.1111/j.1365-2958.1988.tb00013.x. PMID: 28776790.
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Folding in vitro and transport in vivo of pre-β-lactamase are SecB independent.

Molecular microbiology

Laminet AA, Kumamoto CA, Plückthun A.
PMID: 28776793
Mol Microbiol. 1991 Jan;5(1):117-122. doi: 10.1111/j.1365-2958.1991.tb01832.x.

The rate of folding of the precursor of β-lactamase is not influenced by the presence of SecB under conditions in which GroEL/ES retards the folding. Wild-type β-lactamase and several mutants in the signal or the mature protein, affecting either...

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Laminet AA, Kumamoto CA, Plückthun A. Folding in vitro and transport in vivo of pre-β-lactamase are SecB independent. Mol Microbiol. 1991;5(1):117-122doi: 10.1111/j.1365-2958.1991.tb01832.x.
Laminet, A. A., Kumamoto, C. A., & Plückthun, A. (1991). Folding in vitro and transport in vivo of pre-β-lactamase are SecB independent. Molecular microbiology, 5(1), 117-122. https://doi.org/10.1111/j.1365-2958.1991.tb01832.x
Laminet, A A, et al. "Folding in vitro and transport in vivo of pre-β-lactamase are SecB independent." Molecular microbiology vol. 5,1 (1991): 117-122. doi: https://doi.org/10.1111/j.1365-2958.1991.tb01832.x
Laminet AA, Kumamoto CA, Plückthun A. Folding in vitro and transport in vivo of pre-β-lactamase are SecB independent. Mol Microbiol. 1991 Jan;5(1):117-122. doi: 10.1111/j.1365-2958.1991.tb01832.x. PMID: 28776793.
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Escherichia coli molecular genetic map (1000Kbp):update.

Molecular microbiology

Medigue C, Hénaut A, Danchin A.
PMID: 28776816
Mol Microbiol. 1990 Sep;4(9):1443-1454. doi: 10.1111/j.1365-2958.1990.tb02055.x.

The sequenced genes from Escherichia coli that are available in the EMBL library (release 21) have been localized on an updated and corrected version of the restriction map of the chromosome generated by kohara et al. (1987). One thousand...

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Medigue C, Hénaut A, Danchin A. Escherichia coli molecular genetic map (1000Kbp):update. Mol Microbiol. 1990;4(9):1443-1454doi: 10.1111/j.1365-2958.1990.tb02055.x.
Medigue, C., Hénaut, A., & Danchin, A. (1990). Escherichia coli molecular genetic map (1000Kbp):update. Molecular microbiology, 4(9), 1443-1454. https://doi.org/10.1111/j.1365-2958.1990.tb02055.x
Medigue, C, et al. "Escherichia coli molecular genetic map (1000Kbp):update." Molecular microbiology vol. 4,9 (1990): 1443-1454. doi: https://doi.org/10.1111/j.1365-2958.1990.tb02055.x
Medigue C, Hénaut A, Danchin A. Escherichia coli molecular genetic map (1000Kbp):update. Mol Microbiol. 1990 Sep;4(9):1443-1454. doi: 10.1111/j.1365-2958.1990.tb02055.x. PMID: 28776816.
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Mutagenesis, cloning and complementation analysis of C.

Molecular microbiology

Hamblin MJ, Shaw JG, Curson JP, Kelly DJ.
PMID: 28776818
Mol Microbiol. 1990 Sep;4(9):1567-1574. doi: 10.1111/j.1365-2958.1990.tb02068.x.

Transposon mutagenesis was used to isolate insertion mutants of the photosynthetic bacterium Rhodobacter capsulatus which were unable to grow under aerobic conditions in the dark on malate, succinate or fumarate as sole carbon sources. Of five mutants isolated, all...

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Hamblin MJ, Shaw JG, Curson JP, et al. Mutagenesis, cloning and complementation analysis of C. Mol Microbiol. 1990;4(9):1567-1574doi: 10.1111/j.1365-2958.1990.tb02068.x.
Hamblin, M. J., Shaw, J. G., Curson, J. P., & Kelly, D. J. (1990). Mutagenesis, cloning and complementation analysis of C. Molecular microbiology, 4(9), 1567-1574. https://doi.org/10.1111/j.1365-2958.1990.tb02068.x
Hamblin, M J, et al. "Mutagenesis, cloning and complementation analysis of C." Molecular microbiology vol. 4,9 (1990): 1567-1574. doi: https://doi.org/10.1111/j.1365-2958.1990.tb02068.x
Hamblin MJ, Shaw JG, Curson JP, Kelly DJ. Mutagenesis, cloning and complementation analysis of C. Mol Microbiol. 1990 Sep;4(9):1567-1574. doi: 10.1111/j.1365-2958.1990.tb02068.x. PMID: 28776818.
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Functional organization of the ends of IS 1: specific binding site for an IS1-encoded protein.

Molecular microbiology

Zerbib D, Prentki P, Gamas P, Freund E, Galas DJ, Chandler M.
PMID: 28776821
Mol Microbiol. 1990 Sep;4(9):1477-1486. doi: 10.1111/j.1365-2958.1990.tb02058.x.

The IS 1-encoded protein InsA binds specifically to both ends of IS 1, and acts as a repressor of IS1 gene expression and may be a direct inhibitor of the transposition process. We show here, using DNasel 'foot-printing' and...

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Zerbib D, Prentki P, Gamas P, et al. Functional organization of the ends of IS 1: specific binding site for an IS1-encoded protein. Mol Microbiol. 1990;4(9):1477-1486doi: 10.1111/j.1365-2958.1990.tb02058.x.
Zerbib, D., Prentki, P., Gamas, P., Freund, E., Galas, D. J., & Chandler, M. (1990). Functional organization of the ends of IS 1: specific binding site for an IS1-encoded protein. Molecular microbiology, 4(9), 1477-1486. https://doi.org/10.1111/j.1365-2958.1990.tb02058.x
Zerbib, D, et al. "Functional organization of the ends of IS 1: specific binding site for an IS1-encoded protein." Molecular microbiology vol. 4,9 (1990): 1477-1486. doi: https://doi.org/10.1111/j.1365-2958.1990.tb02058.x
Zerbib D, Prentki P, Gamas P, Freund E, Galas DJ, Chandler M. Functional organization of the ends of IS 1: specific binding site for an IS1-encoded protein. Mol Microbiol. 1990 Sep;4(9):1477-1486. doi: 10.1111/j.1365-2958.1990.tb02058.x. PMID: 28776821.
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Showing 1 to 12 of 392 entries