Biocatalytic Synthesis of Bioactive Compounds
Biocatalysis, the application of enzymes as catalysts for chemical synthesis, has become an increasingly valuable tool for the synthetic chemist. Enzymatic transformations carried out by enzymes or whole-cell catalysts are used for the production of a wide variety of compounds ranging from bulk to f...
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Format: | Electronic Book Chapter |
Language: | English |
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Basel, Switzerland
MDPI - Multidisciplinary Digital Publishing Institute
2020
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Online Access: | DOAB: download the publication DOAB: description of the publication |
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700 | 1 | |a Aleu, Josefina |4 oth | |
245 | 1 | 0 | |a Biocatalytic Synthesis of Bioactive Compounds |
260 | |a Basel, Switzerland |b MDPI - Multidisciplinary Digital Publishing Institute |c 2020 | ||
300 | |a 1 electronic resource (142 p.) | ||
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506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
520 | |a Biocatalysis, the application of enzymes as catalysts for chemical synthesis, has become an increasingly valuable tool for the synthetic chemist. Enzymatic transformations carried out by enzymes or whole-cell catalysts are used for the production of a wide variety of compounds ranging from bulk to fine chemicals. The primary consideration for the incorporation of biotransformation in a synthetic sequence is regio- and stereocontrol that can be achieved with enzyme-catalyzed reactions. Biotransformations are thus becoming accepted as a method for generating optically pure compounds as well as for developing efficient routes to target compounds. This Special Issue aims to address the main applications of biocatalysts, isolated enzymes, and whole microorganisms in the synthesis of bioactive compounds and their precursors. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Research & information: general |2 bicssc | |
650 | 7 | |a Biology, life sciences |2 bicssc | |
653 | |a 8-hydroxydaidzein | ||
653 | |a stable | ||
653 | |a soluble | ||
653 | |a anti-inflammation | ||
653 | |a amylosucrase | ||
653 | |a Deinococcus geothermalis | ||
653 | |a coumarin | ||
653 | |a biotransformation | ||
653 | |a filamentous fungi | ||
653 | |a selective hydroxylation | ||
653 | |a bromination | ||
653 | |a chlorination | ||
653 | |a pharmaceuticals | ||
653 | |a active agent synthesis | ||
653 | |a biocatalysis | ||
653 | |a haloperoxidase | ||
653 | |a halogenase | ||
653 | |a glycosyltransferase | ||
653 | |a Glycine max (L.) Merr. | ||
653 | |a HPLC/MS | ||
653 | |a isoflavone aglycone-rich extract | ||
653 | |a isoflavone α-glucoside | ||
653 | |a alkene cleavage | ||
653 | |a aryl alkenes | ||
653 | |a basidiomycota | ||
653 | |a carotene degradation | ||
653 | |a dye-decolorizing peroxidase (DyP) | ||
653 | |a manganese | ||
653 | |a Komagataella pfaffii | ||
653 | |a Pleurotus sapidus | ||
653 | |a monoterpenes | ||
653 | |a limonene | ||
653 | |a glycerol | ||
653 | |a mevalonate pathway | ||
653 | |a reaction engineering | ||
653 | |a bioprocess | ||
653 | |a biocatalyst | ||
653 | |a two-liquid phase fermentation | ||
653 | |a in situ product removal | ||
653 | |a lipase | ||
653 | |a unsaturated fatty acid | ||
653 | |a oxidative cleavage | ||
653 | |a oxidation | ||
653 | |a adaptation | ||
653 | |a UV/NTG mutagenesis | ||
653 | |a psychrotrophs | ||
653 | |a terpenes | ||
856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/3150 |7 0 |z DOAB: download the publication |
856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/69357 |7 0 |z DOAB: description of the publication |