Evidence map›Paper›PMID 26697108›Full record

ArticleBiotechnology for biofuels2015

Short-term adaptation during propagation improves the performance of xylose-fermenting Saccharomyces cerevisiae in simultaneous saccharification and co-fermentation.

Fredrik Nielsen, Elia Tomás-Pejó, Lisbeth Olsson, Ola Wallberg

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 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Automated yeast cultivation control using a biosensor and flow cytometry.Journal of industrial microbiology & biotechnology · 2024
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  10. Genomic and transcriptomic analysis ofBiotechnology for biofuels · 2020
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  13. Physiological mechanism of improved tolerance ofBiotechnology for biofuels · 2019
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  14. Seed culture pre-adaptation ofBiotechnology for biofuels · 2019
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  15. Augmenting Pentose Utilization and Ethanol Production of NativeFrontiers in bioengineering and biotechnology · 2018
    Article
  16. Review
  17. Increased lignocellulosic inhibitor tolerance ofBiotechnology for biofuels · 2017
    Article
  18. Article
  19. Biotechnology for biofuels · 2017
    Article
  20. Article
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

4 authors at 2 institutions in 1 country.

Fredrik NielsenDepartment of Chemical Engineering, Lund University, P.O. Box 124, 221 00 Lund, Sweden.ORCID 0000-0002-8988-0336
Elia Tomás-PejóDepartment of Biology and Biological Engineering, Industrial Biotechnology, Chalmers University of Technology, SE-412 96 Göteborg, Sweden ; Unit of Biotechnological Processes for Energy Production, IMDEA Energy, 28935 Móstoles, Spain.
Lisbeth OlssonDepartment of Biology and Biological Engineering, Industrial Biotechnology, Chalmers University of Technology, SE-412 96 Göteborg, Sweden.
Ola WallbergDepartment of Chemical Engineering, Lund University, P.O. Box 124, 221 00 Lund, Sweden.
Chalmers University of Technology · SELund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInhibitors that are generated during thermochemical pretreatment and hydrolysis impair the performance of microorganisms during fermentation of lignocellulosic hydrolysates. In omitting costly detoxification steps, the fermentation process relies extensively on the performance of the fermenting microorganism. One attractive option of improving its performance and tolerance to microbial inhibitors is short-term adaptation during propagation. This study determined the influence of short-term adaptation on the performance of recombinant Saccharomyces cerevisiae in simultaneous saccharification and co-fermentation (SSCF). The aim was to understand how short-term adaptation with lignocellulosic hydrolysate affects the cell mass yield of propagated yeast and performance in subsequent fermentation steps. The physiology of propagated yeast was examined with regard to viability, vitality, stress responses, and upregulation of relevant genes to identify any links between the beneficial traits that are promoted during adaptation and overall ethanol yields in co-fermentation.

resultsThe presence of inhibitors during propagation significantly improved fermentation but lowered cell mass yield during propagation. Xylose utilization of adapted cultures was enhanced by increasing amounts of hydrolysate in the propagation. Ethanol yields improved by over 30 % with inhibitor concentrations that corresponded to ≥2.5 % water-insoluble solids (WIS) load during the propagation compared with the unadapted culture. Adaptation improved cell viability by >10 % and increased vitality by >20 %. Genes that conferred resistance against inhibitors were upregulated with increasing amounts of inhibitors during the propagation, but the adaptive response was not associated with improved ethanol yields in SSCF. The positive effects in SSCF were observed even with adaptation at inhibitor concentrations that corresponded to 2.5 % WIS. Higher amounts of hydrolysate in the propagation feed further improved the fermentation but increased the variability in fermentation outcomes and resulted in up to 20 % loss of cell mass yield.

conclusionsShort-term adaptation during propagation improves the tolerance of inhibitor-resistant yeast strains to inhibitors in lignocellulosic hydrolysates and improves their ethanol yield in fermentation and xylose-fermenting capacity. A low amount of hydrolysate (corresponding to 2.5 % WIS) is optimal, whereas higher amounts decrease cell mass yield during propagation.

Indexed as

Co-fermentationLignocellulosePre-adaptationPropagationXyloseYeast

Identifiers

PMID26697108
PMCPMC4687142
OpenAlexW2212178179

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.