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AtpE ATP synthase epsilon chain

Top mentioned proteins: atpB, ACID, ATPase, CAN, HAD
Papers on atpE
Model-aided atpE gene knockout strategy in Escherichia coli for enhanced succinic acid production from glycerol.
Md Illias et al., Johor Bahru, Malaysia. In J Biomol Struct Dyn, Jan 2016
Herein, we report what are, to our knowledge, the first metabolic knockout of the atpE gene to have increased succinic acid production using both glucose and alternative glycerol carbon sources in E. coli.
Complete plastid genome of Astragalus mongholicus var. nakaianus (Fabaceae).
Choi et al., Inch'ŏn, South Korea. In Mitochondrial Dna, Jul 2015
The putative pseudogene with abnormal stop codons is atpE.
Exploration of the mechanisms of biofilm formation by Enterococcus faecalis in glucose starvation environments.
Liang et al., Shanghai, China. In Aust Dent J, Jun 2015
In addition, transcription of ace, fsrB and gelE genes increased under glucose starvation stress while atpE, salB and esp genes were down-regulated.
Preliminary study of two steps aqueous two-phase extraction combined with high performance liquid chromatography for saliva protein selective separation.
Luo et al., In Se Pu, 2014
Saliva protein separation by one-step aqueous two-phase extraction (ATPE) in the system of 15% (mass ratio if not specified) PEG-4000/8% NaH2PO4 was presented.
Magnetic aqueous two phase fishing: a hybrid process technology for antibody purification.
Roque et al., Caparica, Portugal. In J Chromatogr A, 2014
The potential to combine aqueous two-phase extraction (ATPE) with magnetic separation was here investigated with the aim of developing a selective non-chromatographic method for the purification of antibodies from cell culture supernatants.
Isolation of monoclonal antibody from a Chinese hamster ovary supernatant. I: assessment of different separation concepts.
Antos et al., Rzeszów, Poland. In J Chromatogr A, 2013
Ion exchange chromatography (IEC), hydrophobic interaction chromatography (HIC), aqueous-two-phase extraction (ATPE) and their integration has been evaluated in terms of yield and purity of the product obtained.
atpE gene as a new useful specific molecular target to quantify Mycobacterium in environmental samples.
Moulin et al., Champs-sur-Marne, France. In Bmc Microbiol, 2012
Based on DNA sequence alignments, we designed primer pairs and a probe that specifically detect the atpE gene of mycobacteria, as verified by quantitative real-time PCR on a collection of mycobacteria and non-mycobacterial species.
Aqueous two-phase extraction as a platform in the biomanufacturing industry: economical and environmental sustainability.
Aires-Barros et al., Lisbon, Portugal. In Biotechnol Adv, 2011
Aqueous two-phase extraction (ATPE) has been successfully revisited as a valuable alternative for the capture of antibodies.
Structure, organization and expression of cyanobacterial ATP synthase genes.
Curtis, Raleigh, United States. In Photosynth Res, 1988
The second cluster of genes, atp 2, contains the remaining two ATP synthase genes in the order atpB-atpE.
Chloroplast messenger RNAs of free and thylakoid-bound polysomes from Vicia faba L.
Hachtel et al., Bonn, Germany. In Planta, 1988
In contrast, transcripts of the genes rbcL, psbE, petD, atpA, atpB, atpE and atpH were found more frequently on free polysomes corresponding to a stroma-located translation of these mRNAs and a posttranslational integration of the encoded intrinsic membrane proteins.
Blue-light control of mRNA level and transcription during chloroplast differentiation in photomixotrophic and photoautotrophic cell cultures (Chenopodium rubrum L.).
Hüsemann et al., Hannover, Germany. In Planta, 1987
During this process of greening the steady-state concentration of mRNAs coding for plastid proteins increases rapidly in response to blue-light exposure as was determined by a dothybridization technique employing cloned DNA sequences complementary to these nuclear and plastid transcripts (light-harvesting chlorophyll a/b protein, rbcs, rbcl, psbA, atpB, atpE).
Chloroplast genes encoding subunits of the H(+)-ATPase complex of Chlamydomonas reinhardtii are rearranged compared to higher plants: sequence of the atpE gene and location of the atpF and atpI genes.
Boynton et al., Durham, United States. In Plant Mol Biol, 1987
The chloroplast gene for the epsilon subunit (atpE) of the CF1/CF0 ATPase in the green alga Chlamydomonas reinhardtii has been localized and sequenced.
Mapping the chloroplast genome of triazine resistant canola.
Straus et al., Toronto, Canada. In Theor Appl Genet, 1986
The genes for rRNA, rbcL, cytF, atpA, atpB, atpE, atpH and the triazine resistance gene, psbA were located on the map by heterologous hybridization.
Positioning of protein-coding genes on the soybean chloroplast genome.
Pillay et al., Windsor, Canada. In Plant Mol Biol, 1985
These include the genes for the alpha, beta and epsilon subunits of the CF1 component of ATP synthase (atpA, atpB and atpE respectively), for subunit III of the CF0 component of ATP synthase (atpH), for the cytochrome f (cytF), for the '32 Kd' thylakoid protein (psbA), and for the large subunit of ribulose-1,5-bisphosphate carboxylase-oxygenase (rbcL), all of which map in the large single copy region.
Physical mapping of genes for chloroplast DNA encoded subunit polypeptides of the ATPsynthase complex from Petunia hybrida.
Nijkamp et al., Amsterdam, Netherlands. In Curr Genet, 1984
The position of the atpB and the atpE gene, encoding respectively the beta and epsilon subunit, on the Sall S9 fragment was determined in more detail by studying polypeptide synthesis directed by subclones of the S9 fragment in E. coli minicells.
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