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Plant biomass degradation supported by non-enzymatic proteins

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Lignocellulosic biomass, rich in potential carbon sources and value added products, has been intensively investigated in scope of its costefficient and effective decomposition. Many methods were developed, physicochemical or biological. Nevertheless, they are either expensive, inefficient or pose threat to the environment. Recently discovered proteins, lacking any hydrolytic activity, can be a key to solve problems associated with a slow process of enzymatical, eco-friendly degradation. These proteins belong to three related groups – swollenins, expansins and loosenins. Using different molecular mechanisms, they disrupt hydrogen bonds within cellulose chains, enabling enzymes to perform hydrolysis leading to decomposition of lignocellulosic complex.
Rocznik
Strony
71--81
Opis fizyczny
Bibliogr. 28 poz., il. (w tym kolor.)
Twórcy
autor
  • Institute of General Food Chemistry, Lodz University of Technology, Stefanowskiego 4/10, 90-924 Lodz
  • Institute of Technical Biochemistry, Lodz University of Technology, Stefanowskiego 4/10, 90-924 Lodz
autor
  • Institute of General Food Chemistry, Lodz University of Technology, Stefanowskiego 4/10, 90-924 Lodz
Bibliografia
  • 1. Shen Y, Yu S, Ge S. Hydrothermal carbonization of medical wastes and lignocellulosic biomass for solid fuel production from lab-scale to pilot-scale. Energy 2017, 118:312-323.
  • 2. Zhao X, Liu W, Deng Y, Zhu JY. Low-temperature microbial and direct conversion of lignocellulosic biomass to electricity: Advances and challenges. Renew Sustainable Energy Rev. 2017, 71:268-282.
  • 3. Morgan HM, Bu Q, Liang J. A review of catalytic microwave pyrolysis of lignocellulosic biomass for value-added fuel and chemicals. Bioresour Technol 2017, 230:112-121.
  • 4. Nilsson RLK, Holgren M, Madavi B. Adaptability of Trametes versicolor to the lignocellulosic inhibitors furfural, HMF, phenol and levulinic acid during ethanol fermentation. Biomass Bioenergy 2016, 90:95-100.
  • 5. Lee HJ, Lim WS, Lee JW. Improvement of ethanol fermentation from lignocellulosic hydrolysates by the removal of inhibitors. J Ind Eng Chem 2013, 19:2010-2015.
  • 6. Mattila H, Kuuskeri J, Lundell T. Single-step, single-organism bioethanol production and bioconversion of lignocellulose waste materials by phlebioid fungal species. Bioresour Technol2017, 225:254-261.
  • 7. Cai C, Xueqing Q. Using polyvinylpyrrolidone to enhance the enzymatic hydrolysis of lignocelluloses by reducing the cellulase non-productive adsorption on lignin. Bioresour Technol 2017, 227:74-81.
  • 8. Voet ED, Voet JD, Pratt CW. Fundamentals of Biochemistry. John Wiley & Sons, USA, 1999, pp. 204-205.
  • 9. Sun Y, Cheng J. Hydrolysis of lignocellulosic materials for ethanol production: a review. Bioresour Technol 2002, 83:1-11.
  • 10. Gleice G, Denilson A. Obtaining xanthan gum impregnated with cellulose microfibrils derived from sugarcane bagasse. Materials Today: proceedings 2015, 2:389-398.
  • 11. Xiang Q, Kim JS, Lee YY. A comprehensive kinetic model for dilute-acid hydrolysis of cellulose. Appl Biochem Biotechnol 2003, 105-108:337-340.
  • 12. Habibi, Y, Lucia LA, Rojas OJ. Cellulose nanocrystals: chemistry, self-assembly, and applications. Chem Rev 2010, 110:3479-3500.
  • 13. Boerjan W, Ralph J, Baucher M. Lignin biosynthesis. Ann Rev Plant Biol 2003, 54:519-546.
  • 14. Galbe M, Zacchi G. Pretreatment of lignocellulosic materials for efficient bioethanol production. Adv Biochem Engin/Biotechn 2007, 108:41-65.
  • 15. Chaturvedi V, Verma P. An overview of key pretreatment processes employed for bioconversion of lignocellulosic biomass into biofuels and value added products. Biotech 2013, 3:415-431.
  • 16. Cosgrove D, Cell wall loosening by expansins. Plant Physiol 1998, 118:333-339.
  • 17. Cosgrove D, Loosening of plant cell wall by expansins. Nature 2000, 407:321-326.
  • 18. Wei W, Yang C, Luo J, Lu C, Wu Y, Yuan S. Synergism between cucumber α-expansin, fungal endoglucanase and pectin lyase. J Plant Physiol 2010, 167:1204-1210.
  • 19. Bunterngsook B, Eurwilaichitr L. Binding characteristics and synergistic effects of bacterial expansins on cellulosic and hemicellulosic substrates. Bioresour Technol 2015, 176:129-135.
  • 20. Shan Z, Yang-yang H. The involvement of expansins in response to water stress during leaf development in wheat. J Plant Physiol 2015, 183:64-74.
  • 21. http://www.personal.psu.edu/fsl/ExpCentral/index.htm
  • 22. Cosgrove D. Plant expansins: diversity and interactions with plant cell walls. Curr Opin Plant Biol 2015, 25:162-172.
  • 23. Saloheimo M, Paloheimo M. Swollenin, a Trichoderma reesei protein with sequence similarity to the plant expansins, exhibits disruption activity on cellulosic materials. Eur J Biochem 2002, 267:4202-4211.
  • 24. Andberg M, Penttila M, Saloheimo M. Swollenin from Trichoderma reesei exhibits hydrolytic activity against cellulosic substrates with features of both endoglucanases and cellobiohydrolases. Biores Technol 2015, 181:105-113.
  • 25. Georgelis N, Nikolaidis N, Cosgrove D. Biochemical analysis of expansin-like proteins from microbes. Carbohydr Polym 2015, 181:105-113.
  • 26. Bocchini-Martins DA, Alves do Prado HF, Leite-Ribeiro RS. Agroindustrial Wastes as Substrates for Microbial Enzymes Production and Source of Sugar for Bioethanol Production. Volume II, Chapter 18. Intech 2011, pp. 319-360.
  • 27. Quiroz-Castaneda R, Anaya-Martinez C, Loosenin, a novel protein with cellulosedisrupting activity from Bjerkandera adusta. Microb Cell Factories 2011, 10:8.
  • 28. Gourlay K, Hu J, Arantes V. Swollenin aids in the amorphogenesis step during the enzymatic hydrolysis of pretreated biomass. Bioresour Technol, 2013, 142:498-503.
Uwagi
Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę (zadania 2017).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-3928bf14-8010-4d61-b671-189ad08fa4d2
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