نتایج جستجو برای: escherichiacoli

تعداد نتایج: 89  

2011
Tânia Teixeira Sérgio Deusdado

We used the software Optferm to model and optimize the bioprocess of escherichia coli fermentation, simulating the conditions of a fed-batch bioreactor. The results, obtained by employing different AI approaches, provided useful orientation for nutrient feed strategies for increased productivity. In conclusion, we believe in silico tools can perform a rapid and valid optimization of bioprocesse...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Jason W Chin Andrew B Martin David S King Lei Wang Peter G Schultz

Benzophenones are among the most useful photocrosslinking agents in biology. We have evolved an orthogonal aminoacyl-tRNA synthetase/tRNA pair that makes possible the in vivo incorporation of p-benzoyl-l-phenylalanine into proteins in Escherichia coli in response to the amber codon, TAG. This unnatural amino acid was incorporated with high translational efficiency and fidelity into the dimeric ...

2001
Timothy E. Elgren

Ribonucleotide reductases provide the only biosynthetic pathway for the generation of deoxyribonuc1eotides.l The Escherichia coli enzyme is a 1 : 1 complex of R1 and R2 proteins;2 the X-ray structure of the latter establishes the presence of two nonheme (p-oxo)diiron(III) clusters in close proximity to Tyr 122,3 which must be oxidized to its radical form to elicit enzyme activity.435 It is the ...

2016
Liyang Yang Chonglong Wang Jia Zhou Seon-Won Kim

BACKGROUND Protoilludene is a valuable sesquiterpene and serves as a precursor for several medicinal compounds and antimicrobial chemicals. It can be synthesized by heterologous expression of protoilludene synthase in Escherichia coli with overexpression of mevalonate (MVA) or methylerythritol-phosphate (MEP) pathway, and farnesyl diphosphate (FPP) synthase. Here, we present E. coli as a cell f...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Tim F Cooper Daniel E Rozen Richard E Lenski

Twelve populations of Escherichia coli, derived from a common ancestor, evolved in a glucose-limited medium for 20,000 generations. Here we use DNA expression arrays to examine whether gene-expression profiles in two populations evolved in parallel, which would indicate adaptation, and to gain insight into the mechanisms underlying their adaptation. We compared the expression profile of the anc...

Journal: :Nigerian Journal of Life Sciences 2022

In this research work, there was analysis of the levels heavy metals and antibioticsensitivity bacteria present from waste dumpsites in Benin City, Edo state. Themethodology involved collection samples triplicates randomdumpsites. The sites were Ekosodin, Oluku Uselu all within City metropolis. Also,standard pour plating method with dilution to 10-3 done isolate organisms soil samples. Analysis...

Journal: :Nucleic acids research 1979
T Ogawa T Okazaki

RNA-linked DNA fragments of T7-infected Escherichiacoli were labeled with [(32)P]orthophosphate invivo. The RNA segments of the labeled fragments were isolated by degrading the DNA portion with the 3'--> 5' exonuclease intrinsic to bacteriophage T4 DNA polymerase and fractionated according to net charge by a DEAE-Sephadex A-25 column chromatography in the presence of 7 M urea. Tri-, tetra- and ...

Journal: :Molecules 2018
Eun-Seok Oh Yeon Lee Won Byoung Chae Jana Jeevan Rameneni Yong-Soon Park Yong Pyo Lim Man-Ho Oh

Protein post-translational modification by phosphorylation is essential for the activity and stability of proteins in higher plants and underlies their responses to diverse stimuli. There are more than 300 leucine-rich repeat receptor-like kinases (LRR-RLKs), a major group of receptor-like kinases (RLKs) that plays an important role in growth, development, and biotic stress responses in higher ...

2014
Rainer Nikolay Renate Schloemer Sabine Schmidt Silke Mueller Anja Heubach Elke Deuerling

While the structure of mature ribosomes is analyzed in atomic detail considerably less is known about their assembly process in living cells. This is mainly due to technical and conceptual hurdles. To analyze ribosome assembly in vivo, we designed and engineered an Escherichiacoli strain--using chromosomal gene knock-in techniques--that harbors large and small ribosomal subunits labeled with th...

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