Enzymes and Biocatalysis
Enzymes, also known as biocatalysts, are proteins produced by living cells and found in a wide range of species, including animals, plants, and microorganisms. Due to their specificity, enzymes are often widely used to catalyze various chemical reactions as proficient biocatalysts in many applicatio...
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Format: | Electronic Book Chapter |
Language: | English |
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Basel
MDPI - Multidisciplinary Digital Publishing Institute
2022
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Online Access: | DOAB: download the publication DOAB: description of the publication |
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072 | 7 | |a GP |2 bicssc | |
072 | 7 | |a PS |2 bicssc | |
100 | 1 | |a Kuo, Chia-Hung |4 edt | |
700 | 1 | |a Huang, Chun-Yung |4 edt | |
700 | 1 | |a Shieh, Chwen-Jen |4 edt | |
700 | 1 | |a Dong, Cheng-Di |4 edt | |
700 | 1 | |a Kuo, Chia-Hung |4 oth | |
700 | 1 | |a Huang, Chun-Yung |4 oth | |
700 | 1 | |a Shieh, Chwen-Jen |4 oth | |
700 | 1 | |a Dong, Cheng-Di |4 oth | |
245 | 1 | 0 | |a Enzymes and Biocatalysis |
260 | |a Basel |b MDPI - Multidisciplinary Digital Publishing Institute |c 2022 | ||
300 | |a 1 electronic resource (244 p.) | ||
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506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
520 | |a Enzymes, also known as biocatalysts, are proteins produced by living cells and found in a wide range of species, including animals, plants, and microorganisms. Due to their specificity, enzymes are often widely used to catalyze various chemical reactions as proficient biocatalysts in many applications. Since enzymes are proteins, they are easily denatured and lose their activity under unfavorable conditions of the surrounding environment. Therefore, in order to prolong the activity of and increase the stability of enzymes, immobilization technology is commonly used for improving the overall efficiency of enzyme catalysis. Recent developments in the discovery of stable enzymes have expanded their uses to encompass organic synthesis and the production of specialized chemicals, pharmaceutical intermediates, and agrochemicals. In order to improve enzyme performance, microbial screening or gene cloning is generally used. It is also common for enzyme studies to use a particular medium for microbiological fermentation in order to produce enzymes. This Special Issue shows that enzymes and biocatalysis have found numerous applications in various fields. These applications include the production of APIs, wastewater treatment, transformation of health ingredients, laundry detergent, fortification of feed, and biocementation. Moreover, there are also studies focusing on the immobilization and production procedures of enzymes. Finally, an extensive review of metagenomics studies related to water and soil has also been included. | ||
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 enzyme identification | ||
653 | |a flavin-dependent halogenases | ||
653 | |a bromination | ||
653 | |a metagenome screening | ||
653 | |a bacterial consortia of Botryococcus braunii | ||
653 | |a bioinformatics | ||
653 | |a animal nutrition | ||
653 | |a enzyme | ||
653 | |a animal feed | ||
653 | |a zootechnical additive | ||
653 | |a digestibility | ||
653 | |a antinutritional factors | ||
653 | |a Aspergillus | ||
653 | |a protease | ||
653 | |a sequential fermentation | ||
653 | |a kinetics | ||
653 | |a thermodynamics | ||
653 | |a lipase | ||
653 | |a immobilization | ||
653 | |a Aspergillus japonicus | ||
653 | |a montmorillonite KSF | ||
653 | |a Bambusa oldhamii | ||
653 | |a phenylalanine ammonia-lyase | ||
653 | |a phenylalanine/tyrosine ammonia-lyase | ||
653 | |a substrate specificity | ||
653 | |a plant secondary metabolism | ||
653 | |a phenylpropanoid | ||
653 | |a small molecule | ||
653 | |a dynamic kinetic resolution | ||
653 | |a levetiracetam | ||
653 | |a nitrile hydratase | ||
653 | |a amino amide | ||
653 | |a amino nitrile | ||
653 | |a HCV | ||
653 | |a NS3 | ||
653 | |a protein expression | ||
653 | |a diagnosis | ||
653 | |a helicase | ||
653 | |a biocatalyst | ||
653 | |a cyanide hydratase | ||
653 | |a nitrilase | ||
653 | |a Exidia glandulosa | ||
653 | |a industrial effluent | ||
653 | |a cokemaking | ||
653 | |a electroplating | ||
653 | |a wastewater treatment | ||
653 | |a free cyanide | ||
653 | |a formamide | ||
653 | |a α-amylase | ||
653 | |a pullulanase | ||
653 | |a Clavispora lusitaniae | ||
653 | |a purification | ||
653 | |a enzyme characterization | ||
653 | |a adsorption of protein mixtures | ||
653 | |a BEICP | ||
653 | |a EICP | ||
653 | |a MICP | ||
653 | |a hydrophobic soils | ||
653 | |a Sporosarcina pasteurii | ||
653 | |a soil | ||
653 | |a water | ||
653 | |a metagenomics | ||
653 | |a enzymes | ||
653 | |a biodiversity | ||
653 | |a docosahexaenoic acid ethyl ester | ||
653 | |a eicosapentaenoic acid ethyl ester | ||
653 | |a packed-bed reactor | ||
653 | |a ultrasonication | ||
653 | |a mass transfer | ||
653 | |a solvent-free | ||
653 | |a ethyl acetate | ||
653 | |a trypsin | ||
653 | |a calcium-binding | ||
653 | |a enzyme engineering | ||
653 | |a n/a | ||
856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/6207 |7 0 |z DOAB: download the publication |
856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/93779 |7 0 |z DOAB: description of the publication |