scholarly journals Novel Propagation Strategy of Saccharomyces cerevisiae for Enhanced Xylose Metabolism during Fermentation on Softwood Hydrolysate

Fermentation ◽  
2021 ◽  
Vol 7 (4) ◽  
pp. 288
Author(s):  
Andreea Cristina Dobrescu ◽  
Henrique César Teixeira Veras ◽  
Cristiano Varrone ◽  
Jan Dines Knudsen

An economically viable production of second-generation bioethanol by recombinant xylose-fermenting Saccharomyces cerevisiae requires higher xylose fermentation rates and improved glucose–xylose co-consumption. Moreover, xylose-fermenting S. cerevisiae recognises xylose as a non-fermentable rather than a fermentable carbon source, which might partly explain why xylose is not fermented into ethanol as efficiently as glucose. This study proposes propagating S. cerevisiae on non-fermentable carbon sources to enhance xylose metabolism during fermentation. When compared to yeast grown on sucrose, cells propagated on a mix of ethanol and glycerol in shake flasks showed up to 50% higher xylose utilisation rate (in a defined xylose medium) and a double maximum fermentation rate, together with an improved C5/C6 co-consumption (on an industrial softwood hydrolysate). Based on these results, an automated propagation protocol was developed, using a fed-batch approach and the respiratory quotient to guide the ethanol and glycerol-containing feed. This successfully produced 71.29 ± 0.91 g/L yeast with an average productivity of 1.03 ± 0.05 g/L/h. These empirical findings provide the basis for the design of a simple, yet effective yeast production strategy to be used in the second-generation bioethanol industry for increased fermentation efficiency.

2017 ◽  
Vol 83 (11) ◽  
Author(s):  
Jeroen G. Nijland ◽  
Hyun Yong Shin ◽  
Leonie G. M. Boender ◽  
Paul P. de Waal ◽  
Paul Klaassen ◽  
...  

ABSTRACT Engineering Saccharomyces cerevisiae for the utilization of pentose sugars is an important goal for the production of second-generation bioethanol and biochemicals. However, S. cerevisiae lacks specific pentose transporters, and in the presence of glucose, pentoses enter the cell inefficiently via endogenous hexose transporters (HXTs). By means of in vivo engineering, we have developed a quadruple hexokinase deletion mutant of S. cerevisiae that evolved into a strain that efficiently utilizes d-xylose in the presence of high d-glucose concentrations. A genome sequence analysis revealed a mutation (Y353C) in the general corepressor CYC8, or SSN6, which was found to be responsible for the phenotype when introduced individually in the nonevolved strain. A transcriptome analysis revealed altered expression of 95 genes in total, including genes involved in (i) hexose transport, (ii) maltose metabolism, (iii) cell wall function (mannoprotein family), and (iv) unknown functions (seripauperin multigene family). Of the 18 known HXTs, genes for 9 were upregulated, especially the low or nonexpressed HXT10, HXT13, HXT15, and HXT16. Mutant cells showed increased uptake rates of d-xylose in the presence of d-glucose, as well as elevated maximum rates of metabolism (V max) for both d-glucose and d-xylose transport. The data suggest that the increased expression of multiple hexose transporters renders d-xylose metabolism less sensitive to d-glucose inhibition due to an elevated transport rate of d-xylose into the cell. IMPORTANCE The yeast Saccharomyces cerevisiae is used for second-generation bioethanol formation. However, growth on xylose is limited by pentose transport through the endogenous hexose transporters (HXTs), as uptake is outcompeted by the preferred substrate, glucose. Mutant strains were obtained with improved growth characteristics on xylose in the presence of glucose, and the mutations mapped to the regulator Cyc8. The inactivation of Cyc8 caused increased expression of HXTs, thereby providing more capacity for the transport of xylose, presenting a further step toward a more robust process of industrial fermentation of lignocellulosic biomass using yeast.


2013 ◽  
Vol 6 (1) ◽  
pp. 168 ◽  
Author(s):  
Lorenzo Favaro ◽  
Marina Basaglia ◽  
Alberto Trento ◽  
Eugéne Van Rensburg ◽  
Maria García-Aparicio ◽  
...  

2009 ◽  
Vol 25 ◽  
pp. S263
Author(s):  
C. Kasavi ◽  
I. Finore ◽  
B. Nicolaus ◽  
E. Toksoy Oner ◽  
B. Kirdar ◽  
...  

2021 ◽  
Author(s):  
Marcello Lima Bertuci ◽  
Mariane Daniella da Silva ◽  
João Pedro Cano ◽  
Crispin Humberto Garcia Cruz

Abstract The production of an alternative form of fuel that replaces fossil fuels has been increasingly studied due to the environmental impacts generated by its excessive use, as well as the depletion of these fossil energy sources. Ethanol obtained from the crushing of sugar cane has been used as a substitute for these fuels, mainly in the automotive area. However, alternative sources are being studied to produce the so called second generation bioethanol. This would avoid competition for food producing agricultural areas and agroindustrial waste is a great source for obtaining it. In general, these residues are not always completely reused and are disposed of inappropriately in the environment, becoming contaminants. Therefore, the use of agroindustrial waste can become a renewable source of energy, in addition to reducing environmental impacts. The objective of this work is to produce second generation bioethanol as an alternative to the one currently used, using the rice husk hydrolyzate by the consortium formed by Saccharomyces cerevisiae and Pachysolen tannophilus . For this, an acid hydrolysis was performed with 2% sulfuric acid during 10 minutes of heating in an autoclave, after which the hydrolyzate was detoxified with the use of activated carbon. The crude and detoxified hydrolysates were used as a substrate for the fermentation medium with an initial concentration of 50 mg/mL of reducing sugars. The fermentation process with the use of both yeasts in the crude hydrolyzate medium, in the detoxified medium and in a synthetic medium composed of glucose, was carried out for 24 h, 30º C, 0 rpm and pH 6.5.The best results for the ethanol production of Saccharomyces cerevisiae was the synthetic medium with 20.6 mg/mL. For the yeast Pachysolen tannophilus , its highest production was in a synthetic medium with 11.67 mg/mL. The intercropping of the two yeasts proved to be efficient with a greater ethanol production reaching 21.5 mg/mL, the hydrolyzed and detoxified media showed great potential for ethanol production both in intercropping and in monoculture


2016 ◽  
Vol 220 ◽  
pp. 161-167 ◽  
Author(s):  
Cátia V.T. Mendes ◽  
Crispin H.G. Cruz ◽  
Diana F.N. Reis ◽  
M. Graça V.S. Carvalho ◽  
Jorge M.S. Rocha

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