Extending the Library of Light‐Dependent Protochlorophyllide Oxidoreductases and their Solvent Tolerance, Stability in Light and Cofactor Flexibility. Issue 16 (28th July 2020)
- Record Type:
- Journal Article
- Title:
- Extending the Library of Light‐Dependent Protochlorophyllide Oxidoreductases and their Solvent Tolerance, Stability in Light and Cofactor Flexibility. Issue 16 (28th July 2020)
- Main Title:
- Extending the Library of Light‐Dependent Protochlorophyllide Oxidoreductases and their Solvent Tolerance, Stability in Light and Cofactor Flexibility
- Authors:
- Schmermund, Luca
Bierbaumer, Sarah
Schein, Viktor K.
Winkler, Christoph K.
Kara, Selin
Kroutil, Wolfgang - Abstract:
- Abstract: Biocatalysis is increasingly used in combination with light to develop new and more sustainable synthetic methods. Thereby, mostly a chemical photocatalyst harvesting the light energy is combined with an established enzymatic reaction, thus the biocatalyst itself does not require the light for its specific reaction. Here we expand the library of an enzyme which requires light for its natural reaction, namely the light‐dependent protochlorophyllide oxidoreductase (LPOR). This enzyme catalyzes the NADPH‐dependent reduction of a C=C in a N ‐heterocycle. Out of five LPORs identified by sequence search, four were found to be well expressible in E. coli and active. Investigating the light intensity, which is an important parameter describing energy input and subsequently may enable fast reaction, it turned out that the four LPORs can stand the maximum light intensity reachable with the equipment used (1450 μmol photons m −2 s −1 ). However, the natural substrate and product were degraded at these conditions, allowing only 15 % of the maximum input (211 μmol photons m −2 s −1 ). Furthermore, the LPORs accepted seven different water miscible solvents with a solvent content of up to 20 % v/v and were active at a pH from 6 to 10. While all LPORs known to date are exclusively NADPH dependent, two LPORs identified here were active also with NADH. The cofactor selectivity could be pinned to three amino acid residues, which interestingly do not directly bind to the cofactor.Abstract: Biocatalysis is increasingly used in combination with light to develop new and more sustainable synthetic methods. Thereby, mostly a chemical photocatalyst harvesting the light energy is combined with an established enzymatic reaction, thus the biocatalyst itself does not require the light for its specific reaction. Here we expand the library of an enzyme which requires light for its natural reaction, namely the light‐dependent protochlorophyllide oxidoreductase (LPOR). This enzyme catalyzes the NADPH‐dependent reduction of a C=C in a N ‐heterocycle. Out of five LPORs identified by sequence search, four were found to be well expressible in E. coli and active. Investigating the light intensity, which is an important parameter describing energy input and subsequently may enable fast reaction, it turned out that the four LPORs can stand the maximum light intensity reachable with the equipment used (1450 μmol photons m −2 s −1 ). However, the natural substrate and product were degraded at these conditions, allowing only 15 % of the maximum input (211 μmol photons m −2 s −1 ). Furthermore, the LPORs accepted seven different water miscible solvents with a solvent content of up to 20 % v/v and were active at a pH from 6 to 10. While all LPORs known to date are exclusively NADPH dependent, two LPORs identified here were active also with NADH. The cofactor selectivity could be pinned to three amino acid residues, which interestingly do not directly bind to the cofactor. Abstract : Biotransformations : The library of light‐dependent protochlorophyllide oxidoreductases (LPORs) was extended and characterized towards solvent tolerance, possible light intensity, pH optimum and cofactor flexibility. NADH dependent LPORs were identified for the first time. … (more)
- Is Part Of:
- ChemCatChem. Volume 12:Issue 16(2020)
- Journal:
- ChemCatChem
- Issue:
- Volume 12:Issue 16(2020)
- Issue Display:
- Volume 12, Issue 16 (2020)
- Year:
- 2020
- Volume:
- 12
- Issue:
- 16
- Issue Sort Value:
- 2020-0012-0016-0000
- Page Start:
- 4044
- Page End:
- 4051
- Publication Date:
- 2020-07-28
- Subjects:
- Biocatalysis -- biotransformations -- C=C reduction -- photocatalysis -- photoenzymes
Catalysis -- Periodicals
541.39505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cctc.202000561 ↗
- Languages:
- English
- ISSNs:
- 1867-3880
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 19179.xml