Engineered reduction of S-adenosylmethionine alters lignin in sorghum.

O-methyltransferases Bioenergy crop Cell wall Monolignols Saccharification

Journal

Biotechnology for biofuels and bioproducts
ISSN: 2731-3654
Titre abrégé: Biotechnol Biofuels Bioprod
Pays: England
ID NLM: 9918300888906676

Informations de publication

Date de publication:
15 Oct 2024
Historique:
received: 28 05 2024
accepted: 15 09 2024
medline: 16 10 2024
pubmed: 16 10 2024
entrez: 15 10 2024
Statut: epublish

Résumé

Lignin is an aromatic polymer deposited in secondary cell walls of higher plants to provide strength, rigidity, and hydrophobicity to vascular tissues. Due to its interconnections with cell wall polysaccharides, lignin plays important roles during plant growth and defense, but also has a negative impact on industrial processes aimed at obtaining monosaccharides from plant biomass. Engineering lignin offers a solution to this issue. For example, previous work showed that heterologous expression of a coliphage S-adenosylmethionine hydrolase (AdoMetase) was an effective approach to reduce lignin in the model plant Arabidopsis. The efficacy of this engineering strategy remains to be evaluated in bioenergy crops. We studied the impact of expressing AdoMetase on lignin synthesis in sorghum (Sorghum bicolor L. Moench). Lignin content, monomer composition, and size, as well as biomass saccharification efficiency were determined in transgenic sorghum lines. The transcriptome and metabolome were analyzed in stems at three developmental stages. Plant growth and biomass composition was further evaluated under field conditions. Results evidenced that lignin was reduced by 18% in the best transgenic line, presumably due to reduced activity of the S-adenosylmethionine-dependent O-methyltransferases involved in lignin synthesis. The modified sorghum features altered lignin monomer composition and increased lignin molecular weights. The degree of methylation of glucuronic acid on xylan was reduced. These changes enabled a ~20% increase in glucose yield after biomass pretreatment and saccharification compared to wild type. RNA-seq and untargeted metabolomic analyses evidenced some pleiotropic effects associated with AdoMetase expression. The transgenic sorghum showed developmental delay and reduced biomass yields at harvest, especially under field growing conditions. The expression of AdoMetase represents an effective lignin engineering approach in sorghum. However, considering that this strategy potentially impacts multiple S-adenosylmethionine-dependent methyltransferases, adequate promoters for fine-tuning AdoMetase expression will be needed to mitigate yield penalty.

Sections du résumé

BACKGROUND BACKGROUND
Lignin is an aromatic polymer deposited in secondary cell walls of higher plants to provide strength, rigidity, and hydrophobicity to vascular tissues. Due to its interconnections with cell wall polysaccharides, lignin plays important roles during plant growth and defense, but also has a negative impact on industrial processes aimed at obtaining monosaccharides from plant biomass. Engineering lignin offers a solution to this issue. For example, previous work showed that heterologous expression of a coliphage S-adenosylmethionine hydrolase (AdoMetase) was an effective approach to reduce lignin in the model plant Arabidopsis. The efficacy of this engineering strategy remains to be evaluated in bioenergy crops.
RESULTS RESULTS
We studied the impact of expressing AdoMetase on lignin synthesis in sorghum (Sorghum bicolor L. Moench). Lignin content, monomer composition, and size, as well as biomass saccharification efficiency were determined in transgenic sorghum lines. The transcriptome and metabolome were analyzed in stems at three developmental stages. Plant growth and biomass composition was further evaluated under field conditions. Results evidenced that lignin was reduced by 18% in the best transgenic line, presumably due to reduced activity of the S-adenosylmethionine-dependent O-methyltransferases involved in lignin synthesis. The modified sorghum features altered lignin monomer composition and increased lignin molecular weights. The degree of methylation of glucuronic acid on xylan was reduced. These changes enabled a ~20% increase in glucose yield after biomass pretreatment and saccharification compared to wild type. RNA-seq and untargeted metabolomic analyses evidenced some pleiotropic effects associated with AdoMetase expression. The transgenic sorghum showed developmental delay and reduced biomass yields at harvest, especially under field growing conditions.
CONCLUSIONS CONCLUSIONS
The expression of AdoMetase represents an effective lignin engineering approach in sorghum. However, considering that this strategy potentially impacts multiple S-adenosylmethionine-dependent methyltransferases, adequate promoters for fine-tuning AdoMetase expression will be needed to mitigate yield penalty.

Identifiants

pubmed: 39407217
doi: 10.1186/s13068-024-02572-8
pii: 10.1186/s13068-024-02572-8
doi:

Types de publication

Journal Article

Langues

eng

Pagination

128

Informations de copyright

© 2024. The Author(s).

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Auteurs

Yang Tian (Y)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.

Yu Gao (Y)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.

Halbay Turumtay (H)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
Department of Energy System Engineering, Karadeniz Technical University, 61830, Trabzon, Turkey.

Emine Akyuz Turumtay (EA)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
Department of Chemistry, Recep Tayyip Erdogan University, 53100, Rize, Turkey.

Yen Ning Chai (YN)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.

Hemant Choudhary (H)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Department of Bioresource and Environmental Security, Sandia National Laboratories, Livermore, CA, 94550, USA.

Joon-Hyun Park (JH)

Forage Genetics International, West Salem, WI, 54669, USA.

Chuan-Yin Wu (CY)

Forage Genetics International, West Salem, WI, 54669, USA.

Christopher M De Ben (CM)

Department of Plant Sciences, University of California-Davis, Davis, CA, 95616, USA.

Jutta Dalton (J)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.

Katherine B Louie (KB)

Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.

Thomas Harwood (T)

Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.

Dylan Chin (D)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Rausser College of Natural Resources, University of California-Berkeley, Berkeley, CA, 94720, USA.

Khanh M Vuu (KM)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.

Benjamin P Bowen (BP)

Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.

Patrick M Shih (PM)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
Department of Plant and Microbial Biology, University of California-Berkeley, Berkeley, CA, 94720, USA.

Edward E K Baidoo (EEK)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.

Trent R Northen (TR)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.

Blake A Simmons (BA)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.

Robert Hutmacher (R)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
University of California, Agriculture and Natural Resources, Kearney Agricultural Research and Extension Center, Parlier, CA, 93648, USA.

Jackie Atim (J)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
University of California, Agriculture and Natural Resources, Kearney Agricultural Research and Extension Center, Parlier, CA, 93648, USA.

Daniel H Putnam (DH)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Department of Plant Sciences, University of California-Davis, Davis, CA, 95616, USA.

Corinne D Scown (CD)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.
Energy & Biosciences Institute, University of California-Berkeley, Berkeley, CA, 94720, USA.
Energy Analysis and Environmental Impacts Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.

Jenny C Mortimer (JC)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
School of Agriculture, Food, and Wine, University of Adelaide, Glen Osmond, South Australia, Australia.

Henrik V Scheller (HV)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA.
Department of Plant and Microbial Biology, University of California-Berkeley, Berkeley, CA, 94720, USA.

Aymerick Eudes (A)

Joint BioEnergy Institute, Emeryville, CA, 94608, USA. ageudes@lbl.gov.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS 978R4468, Berkeley, CA, 94720, USA. ageudes@lbl.gov.

Classifications MeSH