A Cobalamin‐Dependent Radical SAM Enzyme Catalyzes the Unique Cα‐Methylation of Glutamine in Methyl‐Coenzyme M Reductase. Issue 32 (29th June 2022)
- Record Type:
- Journal Article
- Title:
- A Cobalamin‐Dependent Radical SAM Enzyme Catalyzes the Unique Cα‐Methylation of Glutamine in Methyl‐Coenzyme M Reductase. Issue 32 (29th June 2022)
- Main Title:
- A Cobalamin‐Dependent Radical SAM Enzyme Catalyzes the Unique Cα‐Methylation of Glutamine in Methyl‐Coenzyme M Reductase
- Authors:
- Gagsteiger, Jana
Jahn, Sören
Heidinger, Lorenz
Gericke, Lukas
Andexer, Jennifer N.
Friedrich, Thorsten
Loenarz, Christoph
Layer, Gunhild - Abstract:
- Abstract: Methyl‐coenzyme M reductase, which is responsible for the production of the greenhouse gas methane during biological methane formation, carries several unique posttranslational amino acid modifications, including a 2‐( S )‐methylglutamine. The enzyme responsible for the Cα ‐methylation of this glutamine is not known. Herein, we identify and characterize a cobalamin‐dependent radical SAM enzyme as the glutamine C‐methyltransferase. The recombinant protein from Methanoculleus thermophilus binds cobalamin in a base‐off, His‐off conformation and contains a single [4Fe‐4S] cluster. The cobalamin cofactor cycles between the methyl‐cob(III)alamin, cob(II)alamin and cob(I)alamin states during catalysis and produces methylated substrate, 5′‐deoxyadenosine and S ‐adenosyl‐l ‐homocysteine in a 1 : 1 : 1 ratio. The newly identified glutamine C‐methyltransferase belongs to the class B radical SAM methyltransferases known to catalyze challenging methylation reactions of sp 3 ‐hybridized carbon atoms. Abstract : The enzyme responsible for the unique Cα ‐methylation of a glutamine residue within methyl‐coenzyme M reductase was identified. Biochemical, spectroscopic and mass spectrometric characterization clearly classify the newly identified glutamine C‐methyltransferase as a cobalamin‐dependent radical SAM enzyme and, thus, as a new member of the class B radical SAM methyltransferase family.
- Is Part Of:
- Angewandte Chemie international edition. Volume 61:Issue 32(2022)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 61:Issue 32(2022)
- Issue Display:
- Volume 61, Issue 32 (2022)
- Year:
- 2022
- Volume:
- 61
- Issue:
- 32
- Issue Sort Value:
- 2022-0061-0032-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-06-29
- Subjects:
- MCR Modification -- Metalloproteins -- Methanogenesis -- Radical Reactions -- Radical S-Adenosylmethionine
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.202204198 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22764.xml