Evidence map›Paper›PMID 33292417›Full record

ArticleBiotechnology for biofuels2020

Promoting the co-utilisation of glucose and xylose in lignocellulosic ethanol fermentations using a data-driven feed-back controller.

Pau Cabaneros Lopez, Isuru Abeykoon Udugama, Sune Tjalfe Thomsen, Christoph Bayer, Helena Junicke, Krist V Gernaey

Abstract read
In one paragraph

Article in Biotechnology for biofuels, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Pau Cabaneros LopezDepartment of Chemical and Biochemical Engineering, PROSYS Research Center, Technical University of Denmark (DTU), Building 228A, 2800, Lyngby, Denmark.ORCID http://orcid.org/0000-0003-2372-5082
Isuru Abeykoon UdugamaDepartment of Chemical and Biochemical Engineering, PROSYS Research Center, Technical University of Denmark (DTU), Building 228A, 2800, Lyngby, Denmark.
Sune Tjalfe ThomsenDepartment of Geosciences and Natural Resource Management, University of Copenhagen, Frederiksberg C, Denmark.
Christoph BayerFaculty of Process Engineering, Technische Hochschule Nürenberg, Nürenberg, Germany.
Helena JunickeDepartment of Chemical and Biochemical Engineering, PROSYS Research Center, Technical University of Denmark (DTU), Building 228A, 2800, Lyngby, Denmark.
Krist V GernaeyDepartment of Chemical and Biochemical Engineering, PROSYS Research Center, Technical University of Denmark (DTU), Building 228A, 2800, Lyngby, Denmark. kvg@kt.dtu.dk.

Funding

Danish Council for Independent Research 7017-00175AEnergy Development and Demonstration Program 64015-0642H2020 Marie Skłodowska-Curie Actions 713683Novo Nordisk Fonden NNF17SA0031362
6 · The paper itself

Abstract

backgroundThe diauxic growth of Saccharomyces cerevisiae on glucose and xylose during cellulose-to-ethanol processes extends the duration of the fermentation and reduces productivity. Despite the remarkable advances in strain engineering, the co-consumption of glucose and xylose is still limited due to catabolite repression. This work addresses this challenge by developing a closed-loop controller that is capable of maintaining the glucose concentration at a steady set-point during fed-batch fermentation. The suggested controller uses a data-driven model to measure the concentration of glucose from 'real-time' spectroscopic data. The concentration of glucose is then automatically controlled using a control scheme that consists of a proportional, integral, differential (PID) algorithm and a supervisory layer that manipulates the feed-rates to the reactor accounting for the changing dynamics of fermentation.

resultsThe PID parameters and the supervisory layer were progressively improved throughout four fed-batch lignocellulosic-to-ethanol fermentations to attain a robust controller able of maintaining the glucose concentration at the pre-defined set-points. The results showed an increased co-consumption of glucose and xylose that resulted in volumetric productivities that are 20-33% higher than the reference batch processes. It was also observed that fermentations operated at a glucose concentration of 10 g/L were faster than those operated at 4 g/L, indicating that there is an optimal glucose concentration that maximises the overall productivity.

conclusionsPromoting the simultaneous consumption of glucose and xylose in S. cerevisiae is critical to increase the productivity of lignocellulosic ethanol processes, but also challenging due to the strong catabolite repression of glucose on the uptake of xylose. Operating the fermentation at low concentrations of glucose allows reducing the effects of the catabolite repression to promote the co-consumption of the two carbon sources. However, S. cerevisiae is very sensitive to changes in the glucose concentration and deviations from a set-point result in notable productivity losses. The controller structure developed and implemented in this work illustrates how combining data-driven measurements of the glucose concentration and a robust yet effective PID-based supervisory control allowed tight control of the concentration of glucose to adjust it to the metabolic requirements of the cell culture that can unlock tangible gains in productivities.

Identifiers

PMID33292417
PMCPMC7672843

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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.