期刊论文详细信息
Biotechnology for Biofuels
Cyanobacterial biomass as carbohydrate and nutrient feedstock for bioethanol production by yeast fermentation
K Benedikt Möllers1  David Cannella3  Henning Jørgensen2  Niels-Ulrik Frigaard1 
[1] Department of Biology, University of Copenhagen, Strandpromenaden 5, 3000 Helsingør, Denmark
[2] Department of Chemical and Biochemical Engineering, Technical University of Denmark, Søltofts Plads, Building 229, 2800 Kgs Lyngby, Denmark
[3] Department of Geosciences and Natural Resource Management, University of Copenhagen, Rolighedsvej 23, 1958 Frederiksberg C, Denmark
关键词: Yeast extract;    Saccharomyces;    Microalgae;    Bioethanol;    Cyanobacteria;   
Others  :  792617
DOI  :  10.1186/1754-6834-7-64
 received in 2013-11-06, accepted in 2014-03-27,  发布年份 2014
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【 摘 要 】

Background

Microbial bioconversion of photosynthetic biomass is a promising approach to the generation of biofuels and other bioproducts. However, rapid, high-yield, and simple processes are essential for successful applications. Here, biomass from the rapidly growing photosynthetic marine cyanobacterium Synechococcus sp. PCC 7002 was fermented using yeast into bioethanol.

Results

The cyanobacterium accumulated a total carbohydrate content of about 60% of cell dry weight when cultivated under nitrate limitation. The cyanobacterial cells were harvested by centrifugation and subjected to enzymatic hydrolysis using lysozyme and two alpha-glucanases. This enzymatic hydrolysate was fermented into ethanol by Saccharomyces cerevisiae without further treatment. All enzyme treatments and fermentations were carried out in the residual growth medium of the cyanobacteria with the only modification being that pH was adjusted to the optimal value. The highest ethanol yield and concentration obtained was 0.27 g ethanol per g cell dry weight and 30 g ethanol L-1, respectively. About 90% of the glucose in the biomass was converted to ethanol. The cyanobacterial hydrolysate was rapidly fermented (up to 20 g ethanol L-1 day-1) even in the absence of any other nutrient additions to the fermentation medium.

Conclusions

Cyanobacterial biomass was hydrolyzed using a simple enzymatic treatment and fermented into ethanol more rapidly and to higher concentrations than previously reported for similar approaches using cyanobacteria or microalgae. Importantly, as well as fermentable carbohydrates, the cyanobacterial hydrolysate contained additional nutrients that promoted fermentation. This hydrolysate is therefore a promising substitute for the relatively expensive nutrient additives (such as yeast extract) commonly used for Saccharomyces fermentations.

【 授权许可】

   
2014 Möllers et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Jørgensen H, Kristensen JB, Felby C: Enzymatic conversion of lignocellulose into fermentable sugars: challenges and opportunities. Biofuels Bioprod Biorefin 2007, 1:119-134.
  • [2]Limayem A, Ricke SC: Lignocellulosic biomass for bioethanol production: current perspectives, potential issues and future prospects. Prog Energy Combust Sci 2012, 38:449-467.
  • [3]Mamo G, Faryar R, Karlsson EN: Microbial glycoside hydrolases for biomass utilization in biofuels applications. In Biofuel Technologies. Edited by Gupta VK, Tuohy MG. Heidelberg: Springer; 2013:171-188.
  • [4]Dismukes GC, Carrieri D, Bennette N, Ananyev GM, Posewitz MC: Aquatic phototrophs: efficient alternatives to land-based crops for biofuels. Curr Opin Biotechnol 2008, 19:235-240.
  • [5]Larkum AW, Ross IL, Kruse O, Hankamer B: Selection, breeding and engineering of microalgae for bioenergy and biofuel production. Trends Biotechnol 2012, 30:198-205.
  • [6]Parmar A, Singh NK, Pandey A, Gnansounou E, Madamwar D: Cyanobacteria and microalgae: a positive prospect for biofuels. Bioresour Technol 2011, 102:10163-10172.
  • [7]Jones CS, Mayfield SP: Algae biofuels: versatility for the future of bioenergy. Curr Opin Biotechnol 2012, 23:346-351.
  • [8]Graham J, Wilcox L, Graham L: Algae. 2nd edition. San Francisco: Benjamin Cummings (Pearson); 2009.
  • [9]Abed R, Dobretsov S, Sudesh K: Applications of cyanobacteria in biotechnology. J Appl Microbiol 2009, 106:1-12.
  • [10]Rosgaard L, de Porcellinis AJ, Jacobsen JH, Frigaard N-U, Sakuragi Y: Bioengineering of carbon fixation, biofuels, and biochemicals in cyanobacteria and plants. J Biotechnol 2012, 162:134-147.
  • [11]Wang B, Wang J, Zhang W, Meldrum DR: Application of synthetic biology in cyanobacteria and algae. Front Microbiol 2012, 3:344.
  • [12]John RP, Anisha G, Nampoothiri KM, Pandey A: Micro and macroalgal biomass: a renewable source for bioethanol. Bioresour Technol 2011, 102:186-193.
  • [13]Aikawa S, Joseph A, Yamada R, Izumi Y, Yamagishi T, Matsuda F, Kawai H, Chang J-S, Hasunuma T, Kondo A: Direct conversion of Spirulina to ethanol without pretreatment or enzymatic hydrolysis processes. Energy Environ Sci 2013, 6:1844-1849.
  • [14]Hoiczyk E, Hansel A: Cyanobacterial cell walls: news from an unusual prokaryotic envelope. J Bacteriol 2000, 182:1191-1199.
  • [15]Domozych DS: Algal cell walls. In eLS. Chichester: John Wiley and Sons; 2011.
  • [16]Allen MM: Cyanobacterial cell inclusions. Annu Rev Microbiol 1984, 38:1-25.
  • [17]Ball SG, Morell MK: From bacterial glycogen to starch: understanding the biogenesis of the plant starch granule. Annu Rev Plant Biol 2003, 54:207-233.
  • [18]Ball S, Colleoni C, Cenci U, Raj JN, Tirtiaux C: The evolution of glycogen and starch metabolism in eukaryotes gives molecular clues to understand the establishment of plastid endosymbiosis. J Exp Bot 2011, 62:1775-1801.
  • [19]Choi SP, Nguyen MT, Sim SJ: Enzymatic pretreatment of Chlamydomonas reinhardtii biomass for ethanol production. Bioresour Technol 2010, 101:5330-5336.
  • [20]Harun R, Danquah MK, Forde GM: Microalgal biomass as a fermentation feedstock for bioethanol production. J Chem Technol Biotechnol 2010, 85:199-203.
  • [21]Harun R, Danquah MK: Influence of acid pre-treatment on microalgal biomass for bioethanol production. Process Biochem 2011, 46:304-309.
  • [22]Harun R, Jason W, Cherrington T, Danquah MK: Exploring alkaline pre-treatment of microalgal biomass for bioethanol production. Appl Energy 2011, 88:3464-3467.
  • [23]Van Baalen C: Studies on marine blue-green algae. Bot Mar 1962, 4:129-139.
  • [24]Stevens S Jr, Balkwill D, Paone D: The effects of nitrogen limitation on the ultrastructure of the cyanobacterium Agmenellum quadruplicatum. Arch Microbiol 1981, 130:204-212.
  • [25]Stevens SE, Paone DA, Balkwill DL: Accumulation of cyanophycin granules as a result of phosphate limitation in Agmenellum quadruplicatum. Plant Physiol 1981, 67:716-719.
  • [26]Beck C, Knoop H, Axmann IM, Steuer R: The diversity of cyanobacterial metabolism: genome analysis of multiple phototrophic microorganisms. BMC Genomics 2012, 13:56. BioMed Central Full Text
  • [27]Luque I, Forchhammer K: Nitrogen assimilation and C/N balance sensing. In The cyanobacteria: molecular biology, genomics and evolution. Edited by Herrero A, Flores E. Norfolk: Caister Academic Press; 2008:335-382.
  • [28]Schwarz R, Forchhammer K: Acclimation of unicellular cyanobacteria to macronutrient deficiency: emergence of a complex network of cellular responses. Microbiology 2005, 151:2503-2514.
  • [29]Sauer J, Schreiber U, Schmid R, Völker U, Forchhammer K: Nitrogen starvation-induced chlorosis in Synechococcus PCC 7942. Low-level photosynthesis as a mechanism of long-term survival. Plant Physiol 2001, 126:233-243.
  • [30]Paone DA, Stevens SE: Nitrogen starvation and the regulation of glutamine synthetase in Agmenellum quadruplicatum. Plant Physiol 1981, 67:1097-1100.
  • [31]Hasunuma T, Kikuyama F, Matsuda M, Aikawa S, Izumi Y, Kondo A: Dynamic metabolic profiling of cyanobacterial glycogen biosynthesis under conditions of nitrate depletion. J Exp Bot 2013, 64:2943-2954.
  • [32]Guerra LT, Xu Y, Bennette N, McNeely K, Bryant DA, Dismukes GC: Natural osmolytes are much less effective substrates than glycogen for catabolic energy production in the marine cyanobacterium Synechococcus sp. strain PCC 7002. J Biotechnol 2013, 166:65-75.
  • [33]Gründel M, Scheunemann R, Lockau W, Zilliges Y: Impaired glycogen synthesis causes metabolic overflow reactions and affects stress responses in the cyanobacterium Synechocystis sp. PCC 6803. Microbiology 2012, 158:3032-3043.
  • [34]Hickman JW, Kotovic KM, Miller C, Warrener P, Kaiser B, Jurista T, Budde M, Cross F, Roberts JM, Carleton M: Glycogen synthesis is a required component of the nitrogen stress response in Synechococcus elongatus PCC 7942. Algal Research 2013, 2:98-106.
  • [35]Xu Y, Tiago Guerra L, Li Z, Ludwig M, Charles Dismukes G, Bryant DA: Altered carbohydrate metabolism in glycogen synthase mutants of Synechococcus sp. strain PCC 7002: cell factories for soluble sugars. Metab Eng 2013, 16:56-67.
  • [36]Kollman VH, Hanners JL, London RE, Adame EG, Walker TE: Photosynthetic preparation and characterization of 13C-labeled carbohydrates in Agmenellum quadruplicatum. Carbohydr Res 1979, 73:193-202.
  • [37]Mahlmann DM, Jahnke J, Loosen P: Rapid determination of the dry weight of single, living cyanobacterial cells using the Mach-Zehnder double-beam interference microscope. Eur J Phycol 2008, 43:355-364.
  • [38]Geider R, La Roche J: Redfield revisited: variability of C: N: P in marine microalgae and its biochemical basis. Eur J Phycol 2002, 37:1-17.
  • [39]Schlegel HG: General Microbiology. Cambridge: Cambridge University Press; 1993.
  • [40]Koch AL: Growth measurement. In Methods for General and Molecular Bacteriology. Edited by Gerhardt P, Murray RGE, Wood WA, Krieg NR. Washington, D.C: American Society for Microbiology; 1994:248-277.
  • [41]Berliner MD, Neely-Fisher D, Rosen B, Fisher R: Spheroplast induction in Anabaena variabilis Kütz and A. azollae stras. Protoplasma 1987, 139:36-40.
  • [42]Sluiter AD, Hames BR, Ruiz RO, Scarlata C, Sluiter JB, Templeton DW, Crocker D: Determination of Structural Carbohydrates and Lignin in Biomass, Technical report NREL/TP-510-42618. National Renewable Energy Laboratory: Golden, Colorado; 2008.
  • [43]Chan-u-tit P, Laopaiboon L, Jaisil P, Laopaiboon P: High level ethanol production by nitrogen and osmoprotectant supplementation under very high gravity fermentation conditions. Energies 2013, 6:884-899.
  • [44]Jones AM, Ingledew W: Fuel alcohol production: appraisal of nitrogenous yeast foods for very high gravity wheat mash fermentation. Process Biochem 1994, 29:483-488.
  • [45]Jørgensen H: Effect of nutrients on fermentation of pretreated wheat straw at very high dry matter content by Saccharomyces cerevisiae. Appl Biochem Biotechnol 2009, 153:44-57.
  • [46]Pereira FB, Guimarães PM, Teixeira JA, Domingues L: Optimization of low-cost medium for very high gravity ethanol fermentations by Saccharomyces cerevisiae using statistical experimental designs. Bioresour Technol 2010, 101:7856-7863.
  • [47]Devantier R, Pedersen S, Olsson L: Characterization of very high gravity ethanol fermentation of corn mash. Effect of glucoamylase dosage, pre-saccharification and yeast strain. Appl Microbiol Biotechnol 2005, 68:622-629.
  • [48]Stevens S, Patterson C, Myers J: The production of hydrogen peroxide by blue‒green algae: a survey. J Phycol 1973, 9:427-430.
  • [49]Verduyn C, Postma E, Scheffers WA, Van Dijken JP: Effect of benzoic acid on metabolic fluxes in yeasts: a continuous‒culture study on the regulation of respiration and alcoholic fermentation. Yeast 1992, 8:501-517.
  • [50]Dubois M, Gilles KA, Hamilton JK, Rebers P, Smith F: Colorimetric method for determination of sugars and related substances. Anal Chem 1956, 28:350-356.
  • [51]Cannella D, Jørgensen H: Do new cellulolytic enzyme preparations affect the industrial strategies for high solids lignocellulosic ethanol production? Biotechnol Bioeng 2013, 111:59-68.
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