Evidence map›Paper›PMID 27279899›Full record

ArticleBiotechnology for biofuels2015

Anaerobic detoxification of acetic acid in a thermophilic ethanologen.

A Joe Shaw, Bethany B Miller, Stephen R Rogers, William R Kenealy, Alex Meola, Ashwini Bhandiwad, W Ryan Sillers, Indraneel Shikhare, David A Hogsett, Christopher D Herring

Open access · goldAbstract read
In one paragraph

Article in Biotechnology for biofuels, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 34 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

A Joe ShawMascoma Corporation, Lebanon, NH 03766 USA ; Novogy Inc., 85 Bolton St, Cambridge, MA 02140 USA.
Bethany B MillerMascoma Corporation, Lebanon, NH 03766 USA.
Stephen R RogersMascoma Corporation, Lebanon, NH 03766 USA.
William R KenealyMascoma Corporation, Lebanon, NH 03766 USA ; Verdezyne Inc., 2715 Loker Avenue West, Carlsbad, CA 92010 USA.
Alex MeolaMascoma Corporation, Lebanon, NH 03766 USA.
Ashwini BhandiwadThayer School of Engineering, Dartmouth College, Hanover, NH 03755 USA ; Energy Biosciences Institute, 2151 Berkeley Way, Berkeley, CA 94704 USA.
W Ryan SillersMascoma Corporation, Lebanon, NH 03766 USA ; Myriant Corporation, 66 Cummings Park, Woburn, MA 01801 USA.
Indraneel ShikhareMascoma Corporation, Lebanon, NH 03766 USA.
David A HogsettMascoma Corporation, Lebanon, NH 03766 USA ; OPX Biotechnologies Inc., 2425 55th Street, Boulder, CO 80301 USA.
Christopher D HerringMascoma Corporation, Lebanon, NH 03766 USA ; Thayer School of Engineering, Dartmouth College, Hanover, NH 03755 USA.
Dartmouth College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe liberation of acetate from hemicellulose negatively impacts fermentations of cellulosic biomass, limiting the concentrations of substrate that can be effectively processed. Solvent-producing bacteria have the capacity to convert acetate to the less toxic product acetone, but to the best of our knowledge, this trait has not been transferred to an organism that produces ethanol at high yield.

resultsWe have engineered a five-step metabolic pathway to convert acetic acid to acetone in the thermophilic anaerobe Thermoanaerobacterium saccharolyticum. The first steps of the pathway, a reversible conversion of acetate to acetyl-CoA, are catalyzed by the native T. saccharolyticum enzymes acetate kinase and phosphotransacetylase. ack and pta normally divert 30% of catabolic carbon flux to acetic acid; however, their re-introduction in evolved ethanologen strains resulted in virtually no acetic acid production. Conversion between acetic acid and acetyl-CoA remained active, as evidenced by rapid (13)C label transfer from exogenous acetate to ethanol. Genomic re-sequencing of six independently evolved ethanologen strains showed convergent mutations in the hfs hydrogenase gene cluster, which when transferred to wildtype T. saccharolyticum conferred a low acid production phenotype. Thus, the mutated hfs genes effectively separate acetic acid production and consumption from central metabolism, despite their intersecting at the common intermediate acetyl-CoA. To drive acetic acid conversion to a less inhibitory product, the enzymes thiolase, acetoacetate:acetate CoA-transferase, and acetoacetate decarboxylase were assembled in T. saccharolyticum with genes from thermophilic donor organisms that do not natively produce acetone. The resultant strain converted acetic acid to acetone and ethanol while maintaining a metabolic yield of 0.50 g ethanol per gram carbohydrate.

conclusionsConversion of acetic acid to acetone results in improved ethanol productivity and titer and is an attractive low-cost solution to acetic acid inhibition.

Indexed as

Acetate detoxificationCellulosic ethanolInhibitorsMetabolic engineering

Identifiers

PMID27279899
PMCPMC4898469
OpenAlexW1543189950

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.