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  • 1
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1991-06-21
    Description: In order to enhance the yield and productivity of metabolite production, researchers have focused almost exclusively on enzyme amplification or other modifications of the product pathway. However, overproduction of many metabolites requires significant redirection of flux distributions in the primary metabolism, which may not readily occur following product deregulation because metabolic pathways have evolved to exhibit control architectures that resist flux alterations at branch points. This problem can be addressed through the use of some general concepts of metabolic rigidity, which include a means for identifying and removing rigid branch points within an experimental framework.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stephanopoulos, G -- Vallino, J J -- New York, N.Y. -- Science. 1991 Jun 21;252(5013):1675-81.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge 02139.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1904627" target="_blank"〉PubMed〈/a〉
    Keywords: Carbon Dioxide/metabolism ; Corynebacterium/*metabolism ; Enzymes/metabolism ; Genetic Engineering/*methods ; Glucose/metabolism ; Lysine/*biosynthesis ; *Metabolism ; NADP/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2004-04-17
    Description: Pathway optimization is difficult to achieve owing to complex, nonlinear, and largely unknown interactions of enzymes, regulators, and metabolites. We report a pathway reconstruction using RNA display-derived messenger RNA-enzyme fusion molecules. These chimeras are immobilized by hybridization of their messenger RNA end with homologous capture DNA spotted on a substrate surface. Enzymes thus immobilized retain activity proportional to the amount of capture DNA, allowing modulation of the relative activity of pathway enzymes. Entire pathways can thus be reconstructed and optimized in vitro from genomic information. We provide concept validation with the sequential reactions catalyzed by luciferase and nucleoside diphosphate kinase and further illustrate this method with the optimization of the five-step pathway for trehalose synthesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jung, Gyoo Yeol -- Stephanopoulos, Gregory -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):428-31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemical Engineering, Massachusetts Institute of Technology, Room 56-469, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087547" target="_blank"〉PubMed〈/a〉
    Keywords: Catalysis ; DNA/genetics/metabolism ; Enzymes, Immobilized/genetics/*metabolism ; Gene Expression ; *Gene Expression Profiling ; *Genetic Engineering ; Glucose/metabolism ; Glucosyltransferases/genetics/metabolism ; Hexokinase/genetics/metabolism ; Kinetics ; Luciferases/genetics/metabolism ; *Metabolism ; Nucleic Acid Hybridization ; Nucleoside-Diphosphate Kinase/genetics/metabolism ; Oligonucleotide Array Sequence Analysis ; Phosphoglucomutase/genetics/metabolism ; Phosphoric Monoester Hydrolases/genetics/metabolism ; *Protein Array Analysis ; Protein Biosynthesis ; RNA, Messenger/*metabolism ; Trehalose/*biosynthesis ; UTP-Glucose-1-Phosphate Uridylyltransferase/genetics/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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