Rational design of flavoprotein oxidases for biocatalytic valorization of lignin-derived monomers Article Swipe
Biocatalytic valorization of lignin-derived phenolic compounds has emerged as a promising biorefinery strategy in the challenging production of value-added fine chemicals. VAO(vanillyl alcohol oxidase)-type oxidases are promising biocatalysts for modifying lignin-derived phenols. Mechanistic studies on the prototype VAO have revealed that a pivotal product intermediate, a quinone methide, is transiently formed and allows several different oxidation reactions. The work described in this thesis aimed to develop robust VAO-type enzymes that selectively oxidize different lignin-derived phenols into valuable chemicals. For this, eugenol oxidase has been comprehensively investigated for tuning the stability, chemoselectivity and activity through sequence-, structure- and computation-aided enzyme engineering. Whole-cell or enzyme cascade reactions were developed to generate high value compounds starting from lignin-derived alkylphenols. Besides, a novel approach for performing biocatalytic oxidative amination via an “enzyme-trapped quinone methide” was developed. This expands the catalytic repertoire of VAO-type oxidases and offers new opportunities for upgrading lignin.
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Metadata
- Type
- dissertation
- Language
- en
- Landing Page
- https://doi.org/10.33612/diss.651654408
- https://research.rug.nl/files/651654410/Complete_thesis.pdf
- OA Status
- gold
- References
- 141
- Related Works
- 10
- OpenAlex ID
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Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4377018824Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.33612/diss.651654408Digital Object Identifier
- Title
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Rational design of flavoprotein oxidases for biocatalytic valorization of lignin-derived monomersWork title
- Type
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dissertationOpenAlex work type
- Language
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enPrimary language
- Publication year
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2023Year of publication
- Publication date
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2023-05-09Full publication date if available
- Authors
-
Yiming GuoList of authors in order
- Landing page
-
https://doi.org/10.33612/diss.651654408Publisher landing page
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https://research.rug.nl/files/651654410/Complete_thesis.pdfDirect link to full text PDF
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YesWhether a free full text is available
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goldOpen access status per OpenAlex
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https://research.rug.nl/files/651654410/Complete_thesis.pdfDirect OA link when available
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Lignin, Chemistry, Quinone methide, Organic chemistry, Biorefinery, Phenols, Monolignol, Enzyme, Combinatorial chemistry, Quinone, Biosynthesis, Raw materialTop concepts (fields/topics) attached by OpenAlex
- Cited by
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0Total citation count in OpenAlex
- References (count)
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141Number of works referenced by this work
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10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.starting | 112 |
| abstract_inverted_index.strategy | 12 |
| abstract_inverted_index.valuable | 76 |
| abstract_inverted_index.amination | 124 |
| abstract_inverted_index.catalytic | 135 |
| abstract_inverted_index.compounds | 5, 111 |
| abstract_inverted_index.described | 59 |
| abstract_inverted_index.developed | 106 |
| abstract_inverted_index.different | 54, 72 |
| abstract_inverted_index.modifying | 29 |
| abstract_inverted_index.oxidation | 55 |
| abstract_inverted_index.oxidative | 123 |
| abstract_inverted_index.promising | 10, 26 |
| abstract_inverted_index.prototype | 36 |
| abstract_inverted_index.reactions | 104 |
| abstract_inverted_index.upgrading | 145 |
| abstract_inverted_index.Whole-cell | 100 |
| abstract_inverted_index.chemicals. | 20, 77 |
| abstract_inverted_index.developed. | 131 |
| abstract_inverted_index.methide” | 129 |
| abstract_inverted_index.performing | 121 |
| abstract_inverted_index.production | 16 |
| abstract_inverted_index.reactions. | 56 |
| abstract_inverted_index.repertoire | 136 |
| abstract_inverted_index.sequence-, | 94 |
| abstract_inverted_index.stability, | 89 |
| abstract_inverted_index.structure- | 95 |
| abstract_inverted_index.Mechanistic | 32 |
| abstract_inverted_index.biorefinery | 11 |
| abstract_inverted_index.challenging | 15 |
| abstract_inverted_index.selectively | 70 |
| abstract_inverted_index.transiently | 49 |
| abstract_inverted_index.value-added | 18 |
| abstract_inverted_index.Biocatalytic | 0 |
| abstract_inverted_index.VAO(vanillyl | 21 |
| abstract_inverted_index.biocatalysts | 27 |
| abstract_inverted_index.biocatalytic | 122 |
| abstract_inverted_index.engineering. | 99 |
| abstract_inverted_index.investigated | 85 |
| abstract_inverted_index.valorization | 1 |
| abstract_inverted_index.alkylphenols. | 115 |
| abstract_inverted_index.intermediate, | 44 |
| abstract_inverted_index.opportunities | 143 |
| abstract_inverted_index.oxidase)-type | 23 |
| abstract_inverted_index.lignin-derived | 3, 30, 73, 114 |
| abstract_inverted_index.comprehensively | 84 |
| abstract_inverted_index.chemoselectivity | 90 |
| abstract_inverted_index.computation-aided | 97 |
| abstract_inverted_index.“enzyme-trapped | 127 |
| cited_by_percentile_year | |
| corresponding_author_ids | https://openalex.org/A5017006950 |
| countries_distinct_count | 0 |
| institutions_distinct_count | 1 |
| citation_normalized_percentile |