期刊论文详细信息
Biotechnology for Biofuels
Impact of osmotic stress and ethanol inhibition in yeast cells on process oscillation associated with continuous very-high-gravity ethanol fermentation
Liang Wang1  Xin-Qing Zhao1  Chuang Xue1  Feng-Wu Bai2 
[1] School of Life Sciences and Biotechnology, Dalian University of Technology, 2 Linggong Rd., Dalian 116023, China
[2] School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 800 Dongchuan Rd., Shanghai 200240, China
关键词: Ethanol inhibition;    Osmotic stress;    Process oscillation;    Saccharomyces cerevisiae;    VHG fermentation;   
Others  :  797902
DOI  :  10.1186/1754-6834-6-133
 received in 2013-05-25, accepted in 2013-08-21,  发布年份 2013
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【 摘 要 】

Background

VHG fermentation is a promising process engineering strategy aiming at improving ethanol titer, and thus saving energy consumption for ethanol distillation and distillage treatment. However, sustained process oscillation was observed during continuous VHG ethanol fermentation, which significantly affected ethanol fermentation performance of the system.

Results

Sustained process oscillation was investigated in continuous VHG ethanol fermentation, and stresses exerted on yeast cells by osmotic pressure from unfermented sugars and ethanol inhibition developed within the fermentation system were postulated to be major factors triggering this phenomenon. In this article, steady state was established for continuous ethanol fermentation with LG medium containing 120 g/L glucose, and then 160 g/L non-fermentable xylose was supplemented into the LG medium to simulate the osmotic stress on yeast cells under the VHG fermentation condition, but the fermentation process was still at steady state, indicating that the impact of osmotic stress on yeast cells was not the main reason for the process oscillation. However, when 30 g/L ethanol was supplemented into the LG medium to simulate the ethanol inhibition in yeast cells under the VHG fermentation condition, process oscillation was triggered, which was augmented with extended oscillation period and exaggerated oscillation amplitude as ethanol supplementation was increased to 50 g/L, but the process oscillation was gradually attenuated when the ethanol supplementations were stopped, and the steady state was restored. Furthermore, gas stripping was incorporated into the continuous VHG fermentation system to in situ remove ethanol produced by Saccharomyces cerevisiae, and the process oscillation was also attenuated, but restored after the gas stripping was interrupted.

Conclusions

Experimental results indicated that ethanol inhibition rather than osmotic stress on yeast cells is one of the main factors triggering the process oscillation under the VHG fermentation condition, and in the meantime gas stripping was validated to be an effective strategy for attenuating the process oscillation.

【 授权许可】

   
2013 Wang et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Bai FW, Anderson WA, Moo-Young M: Ethanol fermentation technologies from sugar and starch feedstocks. Biotechnol Adv 2008, 26:89-105.
  • [2]Sánchez ÓJ, Cardona CA: Trends in biotechnological production of fuel ethanol from different feedstocks. Bioresour Technol 2008, 99:5270-5295.
  • [3]Meredith J: Dryhouse design: focusing on reliability and return on investment. In The alcohol textbook. Edited by Jacques KA, Lyons TP, Kelsall DR. Nottingham: Nottingham University Press; 2003:255-361.
  • [4]Bayrock DP, Ingledew WM: Application of multistage continuous fermentation for production of fuel alcohol by very-high-gravity fermentation technology. J Ind Microbiol Biotechnol 2001, 27:87-93.
  • [5]Bai FW, Chen LJ, Anderson WA, Moo-Young M: Parameter oscillations in a very high gravity medium continuous ethanol fermentation and their attenuation on a multistage packed column bioreactor system. Biotechnol Bioeng 2004, 88:558-566.
  • [6]Chance B, Estabrook RW, Ghosh A: Damped sinusoidal oscillations of cytoplasmic reduced pyridine nucleotide in yeast cells. Proc Natl Acad Sci USA 1964, 51:1244-1251.
  • [7]Ghosh A, Chance B: Oscillations of glycolytic intermediates in yeast cells. Biochem Biophys Res Commun 1964, 16:174-181.
  • [8]Higgins J: A chemical mechanism for oscillation of glycolytic intermediates in yeast cells. Proc Natl Acad Sci USA 1964, 51:989-994.
  • [9]Richard P, Bakker BM, Teusink B, Van Dam K, Westerhoff HV: Acetaldehyde mediates the synchronization of sustained glycolytic oscillations in populations of yeast cells. Eur J Biochem 1996, 235:238-241.
  • [10]Wolf J, Passarge J, Somsen OJ, Snoep JL, Heinrich R, Westerhoff HV: Transduction of intracellular and intercellular dynamics in yeast glycolytic oscillations. Biophys J 2000, 78:1145-1153.
  • [11]Reijenga KA, Snoep JL, Diderich JA, van Verseveld HW, Westerhoff HV, Teusink B: Control of glycolytic dynamics by hexose transport in Saccharomyces cerevisiae. Biophys J 2001, 80:626-634.
  • [12]Chen CI, McDonald KA, Bisson L: Oscillatory behavior of Saccharomyces cerevisiae in continuous culture: I. Effects of pH and nitrogen levels. Biotechnol Bioeng 1990, 36:19-27.
  • [13]Chen CI, McDonald KA: Oscillatory behavior of Saccharomyces cerevisiae in continuous culture: II. Analysis of cell synchronization and metabolism. Biotechnol Bioeng 1990, 36:28-38.
  • [14]Murray DB, Klevecz RR, Lloyd D: Generation and maintenance of synchrony in Saccharomyces cerevisiae continuous culture. Exp Cell Res 2003, 287:10-15.
  • [15]Satroutdinov AD, Kuriyama H, Kobayashi H: Oscillatory metabolism of Saccharomyces cerevisiae in continuous culture. FEMS Microbiol Lett 1992, 98:261-268.
  • [16]Duboc P, Marison I, von Stockar U: Physiology of Saccharomyces cerevisiae during cell cycle oscillations. J Biotechnol 1996, 51:57-72.
  • [17]Patnaik PR: Oscillatory metabolism of Saccharomyces cerevisiae: an overview of mechanisms and models. Biotechnol Adv 2003, 21:183-192.
  • [18]Devantier R, Scheithauer B, Villas-Bôas SG, Pedersen S, Olsson L: Metabolite profiling for analysis of yeast stress response during very high gravity ethanol fermentations. Biotechnol Bioeng 2005, 90:703-714.
  • [19]Stanley D, Bandara A, Fraser S, Chambers PJ, Stanley GA: The ethanol stress response and ethanol tolerance of Saccharomyces cerevisiae. J Appl Microbiol 2010, 109:13-24.
  • [20]Wang ZX, Zhuge J, Fang H, Prior BA: Glycerol production by microbial fermentation: a review. Biotechnol Adv 2001, 19:201-223.
  • [21]Li LL, Ye YR, Pan L, Zhu Y, Zheng SP, Lin Y: The induction of trehalose and glycerol in Saccharomyces cerevisiae in response to various stresses. Biochem Biophys Res Commun 2009, 387:778-783.
  • [22]Vriesekoop F, Haass C, Pamment NB: The role of acetaldehyde and glycerol in the adaption to ethanol stress of Saccharomyces cerevisiae and other yeasts. FEMS Yeast Res 2009, 9:365-371.
  • [23]Daugulis AJ, McLellan PJ, Li J: Experimental investigation and modeling of oscillatory behavior in the continuous culture of Zymomonas mobilis. Biotechnol Bioeng 1997, 56:99-105.
  • [24]Thomas KC, Hynes SH, Ingledew WM: Practical and theoretical considerations in the production of high concentrations of alcohol by fermentation. Process Biochem 1996, 31:321-331.
  • [25]Lee KJ, Tribe DE, Rogers PL: Ethanol production by Zymomonas mobilis in continuous culture at high glucose concentrations. Biotechnol Lett 1979, 1:421-426.
  • [26]Bai FW, Ge XM, Anderson WA, Moo-Young M: Parameter oscillation attenuation and mechanism exploration for continuous VHG ethanol fermentation. Biotechnol Bioeng 2009, 102:113-121.
  • [27]Csonka LN: Physiological and genetic responses of bacteria to osmotic stress. Microbiol Mol Biol Rev 1989, 53:121-147.
  • [28]Bai FW, Chen LJ, Zhang Z, Anderson WA, Moo-Young M: Continuous ethanol production and evaluation of yeast cell lysis and viability loss under very high gravity medium conditions. J Biotechnol 2004, 110:287-293.
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