Augmentation of ethanol production through statistically designed growth and fermentation medium using novel thermotolerant yeast isolates

2017 ◽  
Vol 109 ◽  
pp. 406-421 ◽  
Author(s):  
Richa Arora ◽  
Shuvashish Behera ◽  
Nilesh Kumar Sharma ◽  
Sachin Kumar
EKUILIBIUM ◽  
2012 ◽  
Vol 11 (2) ◽  
Author(s):  
Margono Margono

<p><strong><em>Abstract:</em></strong> <em>Renewable energy necesity have promote research on ethanol production technology. Ethanol is the potential renewable energy substituting gasoline. However, the conventional problem is high price of the ethanol. The objective of this research was to test the performance of alternative process in producing ethanol, i.e. combination of fermentation process with ethanol stripping in trickle bed bioreactor. The experimental was using Saccharomyces cerevisiae FNCC 3012 and sugarcane bagass as bed particle. It was devided into 2 process steps of biofilm development and ethanol production. Biofilm development was done by circulating medium in bioreactor aerobically. Duration of the biofilm development was 24 hours and followed by ethanol production step which was combinating anaerobic fermentation and stripping process using nitrogen. Production process was conducted for 36 hours lifetime. This method resulted biofilm developing in fermentation medium, not on baggas surfaces. Consequently, ethanol production happened in circulated fermentation medium. The productivity of this method of ethanol production process was not better than the conventional process. Neverherless, the experimental showed that the product stripping and fermentation could be done simultaneously. The stripping process increased ethanol product concentration up to 25% higher than in the broth</em>.</p><p> <strong><em>Keywords:</em></strong> <em>ethanol, Saccharomyces cerevisiae FNCC 3012, trickle bed bioreactor, stripping, biofilm</em></p>


2018 ◽  
Vol 49 (2) ◽  
pp. 378-391 ◽  
Author(s):  
Nuttaporn Chamnipa ◽  
Sudarat Thanonkeo ◽  
Preekamol Klanrit ◽  
Pornthap Thanonkeo

2020 ◽  
Author(s):  
Cleiton Dias do Prado ◽  
Gustavo Patricio Lorca Mandrujano ◽  
Jonas Paulino de Souza ◽  
Flavia Beatriz Sgobbi ◽  
Hosana Ribeiro Novaes ◽  
...  

Abstract Background The use of thermotolerant yeast strains can improve the efficiency of ethanol fermentation, allowing fermentation to occur at temperatures higher than 40 °C. This increment in temperature could benefit traditional bio-ethanol production and allow simultaneous saccharification and fermentation (SSF) of starch or lignocellulosic biomass. Results We identified and characterized the physiology of a new thermotolerant strain able to fermentate at 40 °C while producing high yields of ethanol. Our results showed that, in comparison to the industrial yeast CAT-1, our strain was more resistant to various stressors generated during the production of first- and second-generation ethanol, and it also was able to change the pattern of genes involved in sucrose assimilation (SUC2 and AGT1). The formation of secondary products of fermentation was different at 40ºC, with reduced expression of genes involved in the formation of glycerol (GPD2), acetate (ALD6 and ALD4), and acetyl-CoA (ACS2). Conclusion The LBGA-01 strain is a thermotolerant strain that modulates the production of key genes, changing metabolic pathways during high-temperature fermentation, and increasing its tolerance to the high concentration of ethanol, sugar, acetic lactic, acetic acid, furfural and HMF. This indicates that this strain can be used to improve first- and second-generation ethanol production in Brazil.


2009 ◽  
pp. 7-13
Author(s):  
Éva Erdei ◽  
Mónika Molnár ◽  
Gyöngyi Gyémánt ◽  
János Harangi ◽  
János Nagy ◽  
...  

Fermentation at high temperature with application of thermotolerant microorganisms is a technological advantage in bioethanol production. Among the yeasts, K. marxianus has outstanding thermotolarance. The industrial application of the IMB3 strain occurs usually at 45C. The final aim of our project is the genetic modification of the K. marxianus CBS712 strain in order to achieve ethanol production at higher temperature than the currently applied. This requires the characterization of the CBS712 strain, with special attention to the determination of the temperature limit of its growth and the amount of the ethanol produced. The temperature limit of growth was 48C in YPD medium. Elevation of the temperature above 45C led to an exponential drop of the cell viability. Ethanol production was tested in shaking flasks, in MYFM medium, under oxigene limited conditions, applying variable concentrations of glucose (12–20%) and different temperatures (45–47 ºC). Preliminary results have revealed that the elevation of glucose concentration increased the amount of ethanol produced. The amount of ethanol (appr. 5%)+ produced at the highest glucose concentration was not different at the tested temperatures (45, 46 and 47 ºC). The observation indicates the potential in raising the thermotolerance of the strain. 


ScienceAsia ◽  
2014 ◽  
Vol 40 (4) ◽  
pp. 268 ◽  
Author(s):  
Chutima Kaewkrajay ◽  
Tida Dethoup ◽  
Savitree Limtong

mBio ◽  
2015 ◽  
Vol 6 (4) ◽  
Author(s):  
Luis Caspeta ◽  
Jens Nielsen

ABSTRACT A major challenge for the production of ethanol from biomass-derived feedstocks is to develop yeasts that can sustain growth under the variety of inhibitory conditions present in the production process, e.g., high osmolality, high ethanol titers, and/or elevated temperatures (≥40°C). Using adaptive laboratory evolution, we previously isolated seven Saccharomyces cerevisiae strains with improved growth at 40°C. Here, we show that genetic adaptations to high temperature caused a growth trade-off at ancestral temperatures, reduced cellular functions, and improved tolerance of other stresses. Thermotolerant yeast strains showed horizontal displacement of their thermal reaction norms to higher temperatures. Hence, their optimal and maximum growth temperatures increased by about 3°C, whereas they showed a growth trade-off at temperatures below 34°C. Computational analysis of the physical properties of proteins showed that the lethal temperature for yeast is around 49°C, as a large fraction of the yeast proteins denature above this temperature. Our analysis also indicated that the number of functions involved in controlling the growth rate decreased in the thermotolerant strains compared with the number in the ancestral strain. The latter is an advantageous attribute for acquiring thermotolerance and correlates with the reduction of yeast functions associated with loss of respiration capacity. This trait caused glycerol overproduction that was associated with the growth trade-off at ancestral temperatures. In combination with altered sterol composition of cellular membranes, glycerol overproduction was also associated with yeast osmotolerance and improved tolerance of high concentrations of glucose and ethanol. Our study shows that thermal adaptation of yeast is suitable for improving yeast resistance to inhibitory conditions found in industrial ethanol production processes. IMPORTANCE Yeast thermotolerance can significantly reduce the production costs of biomass conversion to ethanol. However, little information is available about the underlying genetic changes and physiological functions required for yeast thermotolerance. We recently revealed the genetic changes of thermotolerance in thermotolerant yeast strains (TTSs) generated through adaptive laboratory evolution. Here, we examined these TTSs’ physiology and computed their proteome stability over the entire thermal niche, as well as their preadaptation to other stresses. Using this approach, we showed that TTSs exhibited evolutionary trade-offs in the ancestral thermal niche, as well as reduced numbers of growth functions and preadaptation to other stresses found in ethanol production processes. This information will be useful for rational engineering of yeast thermotolerance for the production of biofuels and chemicals.


2020 ◽  
Vol 14 (4) ◽  
pp. 121-128
Author(s):  
DAROJATUL ULYA ◽  
◽  
RIKAINDRI ASTUTI ◽  
ANJA MERYANDINI ◽  
◽  
...  

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