1996
DOI: 10.1021/bk-1996-0626.ch015
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Environmentally Benign Production of Commodity Chemicals Through Biotechnology

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Cited by 7 publications
(2 citation statements)
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“…More sophisticated rational approaches, in which pathways are manipulated through the replacement or alteration of the genes normally present, have replaced the classical random mutagenesis [110,143,144]. Among several methods developed recently, metabolic pathway engineering [145] and combinatorial biosynthesis [146] have garnered the most attention, due to their effectiveness in generating new chemical entities. The basic premise of these methods is that genes from different organisms are combined and expressed in a single host strain in an attempt to reroute the biosynthetic intermediates to new final products.…”
Section: Glycodiversification Via Pathway Engineeringmentioning
confidence: 99%
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“…More sophisticated rational approaches, in which pathways are manipulated through the replacement or alteration of the genes normally present, have replaced the classical random mutagenesis [110,143,144]. Among several methods developed recently, metabolic pathway engineering [145] and combinatorial biosynthesis [146] have garnered the most attention, due to their effectiveness in generating new chemical entities. The basic premise of these methods is that genes from different organisms are combined and expressed in a single host strain in an attempt to reroute the biosynthetic intermediates to new final products.…”
Section: Glycodiversification Via Pathway Engineeringmentioning
confidence: 99%
“…Utilizing a high-throughput colorimetric screen, one particular GalK mutant carrying a single amino acid exchange (Y371H) was obtained in a single round of random mutagenesis on the galactokinase (galK ) gene from E. coli . GalK Y371H displays a surprisingly substantial degree of kinase activity toward sugars as diverse as D-talose (142), L-altrose (141), D-galacturonic acid (144), and L-glucose (145), all of which were not substrates for the wild-type GalK (Scheme 15b). This mutant tolerates substitutions at C-2, C-3, C-5, and C-6 of D-galactose, but maintains a stringent requirement for the axial 4-OH group.…”
Section: Scheme 15mentioning
confidence: 99%