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Title: Directed plant cell-wall accumulation of iron: Embedding co-catalyst for efficient biomass conversion

Abstract

Plant lignocellulosic biomass is an abundant, renewable feedstock for the production of biobased fuels and chemicals. Previously, we showed that iron can act as a co-catalyst to improve the deconstruction of lignocellulosic biomass. However, directly adding iron catalysts into biomass prior to pretreatment is diffusion limited, and increases the cost of biorefinery operations. Recently, we developed a new strategy for expressing iron-storage protein ferritin intracellularly to accumulate iron as a catalyst for the downstream deconstruction of lignocellulosic biomass. In this study, we extend this approach by fusing the heterologous ferritin gene with a signal peptide for secretion into Arabidopsis cell walls (referred to here as FerEX).

Authors:
 [1];  [2];  [1];  [1];  [3];  [4];  [4];  [5];  [6];  [6];  [3];  [1];  [1]; ORCiD logo [1]
+ Show Author Affiliations
  1. National Renewable Energy Lab. (NREL), Golden, CO (United States)
  2. USDA Forest Service, Madison, WI (United States)
  3. Purdue Univ., West Lafayette, IN (United States)
  4. Argonne National Lab. (ANL), Argonne, IL (United States)
  5. National Renewable Energy Lab. (NREL), Golden, CO (United States); Michigan State Univ., East Lansing, MI (United States)
  6. Univ. of Maryland, College Park, MD (United States)
Publication Date:
Research Org.:
National Renewable Energy Laboratory (NREL), Golden, CO (United States); Energy Frontier Research Centers (EFRC) (United States). Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio); Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES); US Department of Agriculture (USDA)
OSTI Identifier:
1331239
Alternate Identifier(s):
OSTI ID: 1377621
Report Number(s):
NREL/JA-2700-67070
Journal ID: ISSN 1754-6834
Grant/Contract Number:  
AC36-08GO28308; SC000997; AC02-06CH11357
Resource Type:
Accepted Manuscript
Journal Name:
Biotechnology for Biofuels
Additional Journal Information:
Journal Volume: 9; Journal Issue: 1; Journal ID: ISSN 1754-6834
Publisher:
BioMed Central
Country of Publication:
United States
Language:
English
Subject:
09 BIOMASS FUELS; ferritin; iron co-catalyst; iron accumulation; transgenic Arabidopsis; biomass; high-throughput hot-water pretreatment; saccharification; sugar release; Perls' Prussian blue staining; X-ray fluorescence microscopy; Perls’ Prussian blue staining; Transgenic Arabidopsis

Citation Formats

Lin, Chien -Yuan, Jakes, Joseph E., Donohoe, Bryon S., Ciesielski, Peter N., Yang, Haibing, Gleber, Sophie -Charlotte, Vogt, Stefan, Ding, Shi -You, Peer, Wendy A., Murphy, Angus S., McCann, Maureen C., Himmel, Michael E., Tucker, Melvin P., and Wei, Hui. Directed plant cell-wall accumulation of iron: Embedding co-catalyst for efficient biomass conversion. United States: N. p., 2016. Web. doi:10.1186/s13068-016-0639-2.
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Lin, Chien -Yuan, Jakes, Joseph E., Donohoe, Bryon S., Ciesielski, Peter N., Yang, Haibing, Gleber, Sophie -Charlotte, Vogt, Stefan, Ding, Shi -You, Peer, Wendy A., Murphy, Angus S., McCann, Maureen C., Himmel, Michael E., Tucker, Melvin P., & Wei, Hui. Directed plant cell-wall accumulation of iron: Embedding co-catalyst for efficient biomass conversion. United States. https://doi.org/10.1186/s13068-016-0639-2
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Lin, Chien -Yuan, Jakes, Joseph E., Donohoe, Bryon S., Ciesielski, Peter N., Yang, Haibing, Gleber, Sophie -Charlotte, Vogt, Stefan, Ding, Shi -You, Peer, Wendy A., Murphy, Angus S., McCann, Maureen C., Himmel, Michael E., Tucker, Melvin P., and Wei, Hui. Fri . "Directed plant cell-wall accumulation of iron: Embedding co-catalyst for efficient biomass conversion". United States. https://doi.org/10.1186/s13068-016-0639-2. https://www.osti.gov/servlets/purl/1331239.
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@article{osti_1331239,
title = {Directed plant cell-wall accumulation of iron: Embedding co-catalyst for efficient biomass conversion},
author = {Lin, Chien -Yuan and Jakes, Joseph E. and Donohoe, Bryon S. and Ciesielski, Peter N. and Yang, Haibing and Gleber, Sophie -Charlotte and Vogt, Stefan and Ding, Shi -You and Peer, Wendy A. and Murphy, Angus S. and McCann, Maureen C. and Himmel, Michael E. and Tucker, Melvin P. and Wei, Hui},
abstractNote = {Plant lignocellulosic biomass is an abundant, renewable feedstock for the production of biobased fuels and chemicals. Previously, we showed that iron can act as a co-catalyst to improve the deconstruction of lignocellulosic biomass. However, directly adding iron catalysts into biomass prior to pretreatment is diffusion limited, and increases the cost of biorefinery operations. Recently, we developed a new strategy for expressing iron-storage protein ferritin intracellularly to accumulate iron as a catalyst for the downstream deconstruction of lignocellulosic biomass. In this study, we extend this approach by fusing the heterologous ferritin gene with a signal peptide for secretion into Arabidopsis cell walls (referred to here as FerEX).},
doi = {10.1186/s13068-016-0639-2},
journal = {Biotechnology for Biofuels},
number = 1,
volume = 9,
place = {United States},
year = {Fri Oct 21 00:00:00 EDT 2016},
month = {Fri Oct 21 00:00:00 EDT 2016}
}
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Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record
https://doi.org/10.1186/s13068-016-0639-2
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Cited by: 12 works
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Figures / Tables:

Fig. 1 Fig. 1: Plant growth images for representative transgenic plants and their Western blot analyses. a Iron‑fertilized empty vector (EV) transgenic control and the transgenic lines expressing heterologous ferritin secreted extracellularly (FerEX). b Plant heights and shoot dry weights (DWs) of the iron‑fertilized EV and FerEX plants at the senescent stage.more » The percentage values inside the brackets are the increases in height or shoot biomass in FerEX lines compared with the EV control. Values are presented as the mean (±SE) of nine plants for each of the lines. * indicates statistical significance of $p$ < 0.05. c PCR analysis of genomic DNA extracted from FerEX, confirming the integration of ferritin transgene into the genome of the transgenic Arabidopsis lines. d Western blotting of ferritin expression levels in cell‑wall protein extracts of plant lines after SDS‑PAGE, using polyclonal anti‑soybean ferritin antibody. e Western blotting of ferritin expression levels in cell‑wall protein extracts of plant lines after native‑PAGE, using polyclonal anti‑soybean ferritin antibody. The illustrated transgenic lines: FerEX(1) and (2) represent FerEX‑8a and ‑10g, respectively« less
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