HEИндивидуална стипендия2025–2027

YcascadE · Design and creation of a yeast platform for synthesis of chiral amines by enzymatic cascades

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

Период
2025-03-01 → 2027-02-28
Финансиране от ЕС
203 464 €
Участници
1
Схема
HORIZON-TMA-MSCA-PF-EF

Линиите свързват координатора с партньорите.

Накратко на български

Дрожди от вида Saccharomyces cerevisiae се модифицират генетично, за да превръщат естествени аминокиселини в хирални амини и аминоалкохоли. Тези вещества са важни междинни продукти при производството на лекарства, торове и специализирани химикали.

Този кратък обзор е генериран от изкуствен интелект

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

Цел на проекта

The development of green and robust technologies for the conversion of renewable feedstock into high-value chemicals is of great interest and challenging for the chemical industry. Although L-α-amino acids can be sustainably produced from renewable feedstock by fermentation, these amino acids are rarely being used as starting material for the chemical synthesis of high-value chiral molecules due to the lack of efficient and highly selective biocatalytic methodologies . In this project, I will design and develop a modular approach for biocatalysis in vivo enabling the conversion of natural amino acids into enantiopure alpha-chiral amines and amino-alcohols, which are important intermediates or final products for the pharmaceutical, agrochemical and fine chemical industries. Saccharomyces cerevisiae will be selected as the host organism for the biocatalytic pathway because its genome is well-known, is suitable for large scale operation, and will allow to obtain higher productivity than using bacterial strains. A library of integrative plasmids expressing the enzymes will be constructed and transformed to S. cerevisiae to obtain a yeast cell factory. The system will be optimized both on the genetic level and on the bioprocess level. The working plan will include an interdisciplinary approach involving molecular biology techniques together with metabolic engineering as well as optimization of conditions for biotransformation. Additionally, analytical chemistry methodologies for determination of yield, purity and enantiomeric excess of the products and intermediates will be required. While the state-of-the-art proves the feasibility of the project, by using our proposed approach with resting S. cerevisiae cells, we expect to make a major break-through in the field in terms of increase productivity (e.g., space-yield; space-time-yield; total yields from substrate) and, moreover, a wider applicability of the resulting platform due to the modularity approach.

Оригинален текст от CORDIS (на английски).

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Връзки

Данни: CORDIS, © Европейски съюз