H2020Индивидуална стипендия2019–2021

Monopoly · Baeyer Villiger Monooxygenases as Biocatalytic Parts for Monomers of New Lactone-based Polymeric Materials

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период
2019-07-15 → 2021-10-09
Финансиране от ЕС
224 934 €
Участници
1
Схема
MSCA-IF

Линиите свързват координатора с партньорите.

Накратко на български

Ензимите BVMO се изследват като инструменти за превръщане на кетони в лактони, които служат за създаване на полимерни материали. Този процес опростява синтеза, избягва страничните продукти и позволява работа при по-меки условия.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Baeyer Villiger Monooxygenases as Biocatalytic Parts for Monomers of New Lactone-based Polymeric Materials

Baeyer-Villiger monooxygenases (BVMOs) are flavoenzymes and belong to the class of oxidoreductases. They catalyse the oxidation of linear, cyclic and aromatic ketones to the corresponding esters or lactones, highly similar to the chemical Baeyer-Villiger oxidation. During the enzymatic oxidation, one atom of molecular oxygen is incorporated into a carbon-carbon bond of a non-activated ketone. Lactones can be produced biocatalytically using Baeyer–Villiger monooxygenases (BVMOs), which are members of a diverse class of flavoprotein monooxygenases. The use of protecting groups and formation of by-products can be avoided in enzymatic processes, simplifying synthesis. BVMOs can show excellent stereoselectivity, and react under relatively mild conditions. Oxidation of ketones by BVMOs, however, is often regio-divergent, generating two lactone products with some substrates. The isomers are produced via migration of the nucleophilic carbon centre, to form the ‘normal’ and ‘abnormal’ isomer, respectively. In Monopoly, we aimed to gain a deeper understanding from a structural/engineering perspective of enzyme catalysis in relation to lactone production by new members of the BVMO family. The overall aim of this Marie Curie CAR fellowship programme is therefore to exploit enzyme kinetics, biocatalysis, structure determination, biophysical analysis and modelling as enabling disciplines to build a tool kit of novel Bayer Villiger monooxygenases as part of a self-consistent Design-Build-Test cycle. Biomaterials composed of lactone monomers have been used to produce polyurethanes. For example, the synthesis of poly--caprolactones takes place via ring-opening polymerisation (ROP) of a monomeric -caprolactones. Additionally, ketal lactones (oxo-carboxylic ketals) are useful in the production of surfactants, plasticisers, solvents and polymers. Monopoly will lead to the development of new lactone monomers from which new polymers could be generated with improved properties and novel applications, especially in the healthcare arena. Biodegradable poly-lactone materials derived from petrochemical routes are already used widely in industry (e.g. speciality polyurethanes, additives, plasticisers), dentistry (as Resilon composites in splints and fillings) and healthcare (e.g. scaffolds for tissue engineering, drug delivery, bio-adhesives and orthopaedic castings). The sustainable production of monomers for these and related polymers is likely to impact in these areas, especially in the healthcare and dentistry markets where high quality/low volume products are sought.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Recent advances in the development of both experimental and computational protein engineering tools have enabled a number of further successes in the development of biocatalysts ready for large-scale applications.The production of monomers from cheap, readily available components (e.g. terpenoids) for sustainable biopolymer synthesis is a growing area of interest. Biomaterials composed of lactone monomers have been used to produce polyurethanes.The present research proposal is focused on the deep understanding of catalysis by newly identified BVMO enzymes, realized through detailed structural and functional analysis of enzyme mechanisms and substrate/coenzyme recognition. This project will involve multidisciplinary training, with clear objectives in the technical areas of synthetic biology, proteomics, structural biology and biophysical chemistry. This project will allow me to work on structure/function relationship of proteins and to extend my knowledge in metabolic pathway engineering especially in understanding of monooxygenases.The objective will be to identify new Baeyer Villiger monooxygenases biocatalysts that have the appropriate biocatalytic and stability characteristics to enable lactone monomer synthesis. The methods would generate novel structural and biocatalytic data to provide a comprehensive toolkit of flavin-dependent BayerVilliger monooxygenases that are suitable for exploitation in lactone monomer synthesis. These new biocatalysts will be used to construct new strains of E. coli that are capable of producing the target lactone monomers in high yield. The immediate outcomes will be new structural information (native and variant forms of the enzymes); new biocatalytic parameters (reactivity profiles with target substrates; stereoselectivity; conversion; stability; coenzyme specificities) and new lactone producing strains generated from existing monoterpene producing E. coli strains.

Оригинален текст от CORDIS (на английски).

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Данни: CORDIS, © Европейски съюз