综述 |
|
|
|
|
蓝藻光驱固碳合成糖类物质的技术研究进展* |
曾雪霞1,2,3,但玉1,2,3,毛绍名1,2,**(),孙佳慧3,4,5,栾国栋3,4,5,**(),吕雪峰3,4,5 |
1. 中南林业科技大学生命科学与技术学院 长沙 410004 2. 中南林业科技大学林业生物技术湖南省重点实验室 长沙 410004 3. 中国科学院青岛生物能源与过程研究所 中国科学院生物燃料重点实验室 青岛 266101 4. 山东能源研究院 青岛 266101 5. 青岛新能源山东省实验室 青岛 266101 |
|
Research Progress on the Cyanobacterial Photosynthetic Production of Sugars Utilizing Carbon Dioxide |
Xue-xia ZENG1,2,3,Yu DAN1,2,3,Shao-ming MAO1,2,**(),Jia-hui SUN3,4,5,Guo-dong LUAN3,4,5,**(),Xue-feng LV3,4,5 |
1. College of Life Science and Technology, Central South University of Forestry and Technology, Changsha 410004, China 2. Hunan Provincial Key Laboratory of Forestry Biotechnology, Central South University of Forestry & Technology, Changsha 410004, China 3. Key Laboratory of Biofuels, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China 4. Shandong Energy Institute, Qingdao 266101, China 5. Qingdao New Energy Shandong Laboratory, Qingdao 266101, China |
引用本文:
曾雪霞,但玉,毛绍名,孙佳慧,栾国栋,吕雪峰. 蓝藻光驱固碳合成糖类物质的技术研究进展*[J]. 中国生物工程杂志, 2022, 42(7): 90-100.
Xue-xia ZENG,Yu DAN,Shao-ming MAO,Jia-hui SUN,Guo-dong LUAN,Xue-feng LV. Research Progress on the Cyanobacterial Photosynthetic Production of Sugars Utilizing Carbon Dioxide. China Biotechnology, 2022, 42(7): 90-100.
链接本文:
https://manu60.magtech.com.cn/biotech/CN/10.13523/j.cb.2203072
或
https://manu60.magtech.com.cn/biotech/CN/Y2022/V42/I7/90
|
[1] |
Dwek R A. Glycobiology: toward understanding the function of sugars. Chemical Reviews, 1996, 96(2): 683-720.
doi: 10.1021/cr940283b
|
[2] |
Zollner N, Heuckenkamp P U. Sugars and sugar substitutes:introduction. Nutr Metab, 1975, 18: R5-R7.
|
[3] |
Ball S G, Morell M K. From bacterial glycogen to starch: understanding the biogenesis of the plant starch granule. Annual Review of Plant Biology, 2003, 54: 207-233.
doi: 10.1146/annurev.arplant.54.031902.134927
|
[4] |
Zacchi L F, Schulz B L. N-glycoprotein macroheterogeneity: biological implications and proteomic characterization. Glycoconjugate Journal, 2016, 33(3): 359-376.
doi: 10.1007/s10719-015-9641-3
pmid: 26638212
|
[5] |
Taylor M E, Drickamer K. Mammalian sugar-binding receptors: known functions and unexplored roles. The FEBS Journal, 2019, 286(10): 1800-1814.
doi: 10.1111/febs.14759
|
[6] |
Mu W M, Zhang W L, Feng Y H, et al. Recent advances on applications and biotechnological production of d-psicose. Applied Microbiology and Biotechnology, 2012, 94(6): 1461-1467.
doi: 10.1007/s00253-012-4093-1
|
[7] |
Dien B S, Cotta M A, Jeffries T W. Bacteria engineered for fuel ethanol production: current status. Applied Microbiology and Biotechnology, 2003, 63(3): 258-266.
pmid: 13680206
|
[8] |
Sasaki K, Tsuge Y, Kawaguchi H, et al. Sucrose purification and repeated ethanol production from sugars remaining in sweet Sorghum juice subjected to a membrane separation process. Applied Microbiology and Biotechnology, 2017, 101(15): 6007-6014.
doi: 10.1007/s00253-017-8316-3
pmid: 28488116
|
[9] |
Sjölin M, Thuvander J, Wallberg O, et al. Purification of sucrose in sugar beet molasses by utilizing ceramic nanofiltration and ultrafiltration membranes. Membranes, 2019, 10(1): 5.
doi: 10.3390/membranes10010005
|
[10] |
Lynd L R. Overview and evaluation of fuel ethanol from cellulosic biomass: technology, economics, the environment, and policy. Annual Review of Energy and the Environment, 1996, 21: 403-465.
doi: 10.1146/annurev.energy.21.1.403
|
[11] |
Golecha R, Gan J B. Biomass transport cost from field to conversion facility when biomass yield density and road network vary with transport radius. Applied Energy, 2016, 164: 321-331.
doi: 10.1016/j.apenergy.2015.11.070
|
[12] |
Zhang T, Yang J G, Tian C Y, et al. High-yield biosynthesis of glucosylglycerol through coupling phosphorolysis and transglycosylation reactions. Journal of Agricultural and Food Chemistry, 2020, 68(51): 15249-15256.
doi: 10.1021/acs.jafc.0c04851
pmid: 33306378
|
[13] |
Wu Y F, Sun X X, Lin Y H, et al. Establishing a synergetic carbon utilization mechanism for non-catabolic use of glucose in microbial synthesis of trehalose. Metabolic Engineering, 2017, 39: 1-8.
doi: 10.1016/j.ymben.2016.11.001
|
[14] |
Rousseaux C, Gregg W. Interannual variation in phytoplankton primary production at A global scale. Remote Sens, 2013, 6: 1-19.
doi: 10.3390/rs6010001
|
[15] |
Flombaum P, Gallegos J L, Gordillo R A, et al. Present and future global distributions of the marine Cyanobacteria Prochlorococcus and Synechococcus. Proceedings of the National Academy of Sciences of the United States of America, 2013, 110(24): 9824-9829.
|
[16] |
Dexter J, Armshaw P, Sheahan C, et al. The state of autotrophic ethanol production in Cyanobacteria. Journal of Applied Microbiology, 2015, 119(1): 11-24.
doi: 10.1111/jam.12821
pmid: 25865951
|
[17] |
Angermayr S A, van der Woude A D, Correddu D, et al. Exploring metabolic engineering design principles for the photosynthetic production of lactic acid by Synechocystis sp.PCC6803. Biotechnology for Biofuels, 2014, 7: 99.
|
[18] |
Gao X, Gao F, Liu D, et al. Engineering the methylerythritol phosphate pathway in cyanobacteria for photosynthetic isoprene production from CO2. Energy & Environmental Science, 2016, 9(4): 1400-1411.
|
[19] |
Hendry J I, Prasannan C, Ma F F, et al. Rerouting of carbon flux in a glycogen mutant of cyanobacteria assessed via isotopically non-stationary 13C metabolic flux analysis. Biotechnology and Bioengineering, 2017, 114(10): 2298-2308.
doi: 10.1002/bit.26350
pmid: 28600876
|
[20] |
Levi C, Preiss J. Regulatory properties of the ADP-glucose pyrophosphorylase of the blue-green bacterium Synechococcus 6301. Plant Physiology, 1976, 58(6): 753-756.
doi: 10.1104/pp.58.6.753
pmid: 16659760
|
[21] |
Feng Y Y, Yao M D, Wang Y, et al. Advances in engineering UDP-sugar supply for recombinant biosynthesis of glycosides in microbes. Biotechnology Advances, 2020, 41: 107538.
doi: 10.1016/j.biotechadv.2020.107538
|
[22] |
Du W, Liang F Y, Duan Y K, et al. Exploring the photosynthetic production capacity of sucrose by cyanobacteria. Metabolic Engineering, 2013, 19: 17-25.
doi: 10.1016/j.ymben.2013.05.001
|
[23] |
Preiss J, Romeo T. Molecular biology and regulatory aspects of glycogen biosynthesis in bacteria. Progress in Nucleic Acid Research and Molecular Biology, 1994, 47: 299-329.
pmid: 8016324
|
[24] |
Guerra L T, Xu Y, Bennette N, et al. Natural osmolytes are much less effective substrates than glycogen for catabolic energy production in the marine cyanobacterium Synechococcus sp.strain PCC 7002. Journal of Biotechnology, 2013, 166(3): 65-75.
doi: 10.1016/j.jbiotec.2013.04.005
pmid: 23608552
|
[25] |
Stal L J, Moezelaar R. Fermentation in cyanobacteria1. FEMS Microbiology Reviews, 1997, 21(2): 179-211.
|
[26] |
Nakamura Y, Takahashi J I, Sakurai A, et al. Some cyanobacteria synthesize semi-amylopectin type α-polyglucans instead of glycogen. Plant and Cell Physiology, 2005, 46(3): 539-545.
doi: 10.1093/pcp/pci045
|
[27] |
Luan G D, Zhang S S, Wang M, et al. Progress and perspective on cyanobacterial glycogen metabolism engineering. Biotechnology Advances, 2019, 37(5): 771-786.
doi: 10.1016/j.biotechadv.2019.04.005
|
[28] |
Aikawa S, Izumi Y, Matsuda F, et al. Synergistic enhancement of glycogen production in Arthrospira platensis by optimization of light intensity and nitrate supply. Bioresource Technology, 2012, 108: 211-215.
doi: 10.1016/j.biortech.2012.01.004
|
[29] |
Aikawa S, Nishida A, Ho S H, et al. Glycogen production for biofuels by the euryhaline cyanobacteria Synechococcus sp. strain PCC 7002 from an oceanic environment. Biotechnology for Biofuels, 2014, 7: 88.
doi: 10.1186/1754-6834-7-88
|
[30] |
Yu J J, Liberton M, Cliften P F, et al. Synechococcus elongatus UTEX 2973, a fast growing cyanobacterial chassis for biosynthesis using light and CO2. Scientific Reports, 2015, 5: 8132.
doi: 10.1038/srep08132
|
[31] |
Song K, Tan X M, Liang Y J, et al. The potential of Synechococcus elongatus UTEX 2973 for sugar feedstock production. Applied Microbiology and Biotechnology, 2016, 100(18): 7865-7875.
doi: 10.1007/s00253-016-7510-z
pmid: 27079574
|
[32] |
Brown A D, Simpson J R. Water relations of sugar-tolerant yeasts: the role of intracellular polyols. Journal of General Microbiology, 1972, 72(3): 589-591.
pmid: 4404634
|
[33] |
Hagemann M. Molecular biology of cyanobacterial salt acclimation. FEMS Microbiology Reviews, 2011, 35(1): 87-123.
doi: 10.1111/j.1574-6976.2010.00234.x
pmid: 20618868
|
[34] |
MacKay M A, Norton R S, Borowitzka L J. Organic osmoregulatory solutes in cyanobacteria. Microbiology, 1984, 130(9): 2177-2191.
doi: 10.1099/00221287-130-9-2177
|
[35] |
Reed R H, Stewart W D P. Osmotic adjustment and organic solute accumulation in unicellular cyanobacteria from freshwater and marine habitats. Marine Biology, 1985, 88(1): 1-9.
doi: 10.1007/BF00393037
|
[36] |
Tan X M, Luo Q, Lu X F. Biosynthesis, biotechnological production, and applications of glucosylglycerols. Applied Microbiology and Biotechnology, 2016, 100(14): 6131-6139.
doi: 10.1007/s00253-016-7608-3
|
[37] |
Zheng S N, Sun H L, Mao S M, et al. Engineering the glycogen metabolism in cyanobacterial photosynthetic cell factories: a review. Chinese Journal of Biotechnology, 2022, 38(2): 592-604.
doi: 10.13345/j.cjb.210230
pmid: 35234384
|
[38] |
Ducat D C, Avelar-Rivas J A, Way J C, et al. Rerouting carbon flux to enhance photosynthetic productivity. Applied and Environmental Microbiology, 2012, 78(8): 2660-2668.
doi: 10.1128/AEM.07901-11
|
[39] |
Hays S G, Yan L L W, Silver P A, et al. Synthetic photosynthetic consortia define interactions leading to robustness and photoproduction. Journal of Biological Engineering, 2017, 11: 4.
doi: 10.1186/s13036-017-0048-5
|
[40] |
Weiss T L, Young E J, Ducat D C. A synthetic, light-driven consortium of cyanobacteria and heterotrophic bacteria enables stable polyhydroxybutyrate production. Metabolic Engineering, 2017, 44: 236-245.
doi: 10.1016/j.ymben.2017.10.009
|
[41] |
Löwe H, Hobmeier K, Moos M, et al. Photoautotrophic production of polyhydroxyalkanoates in a synthetic mixed culture of Synechococcus elongatus cscB and Pseudomonas putida cscAB. Biotechnology for Biofuels, 2017, 10: 190.
doi: 10.1186/s13068-017-0875-0
|
[42] |
Fedeson D T, Saake P, Calero P, et al. Biotransformation of 2, 4-dinitrotoluene in a phototrophic co-culture of engineered Synechococcus elongatus and Pseudomonas putida. Microbial Biotechnology, 2020, 13(4): 997-1011.
doi: 10.1111/1751-7915.13544
pmid: 32064751
|
[43] |
Qiao C C, Duan Y K, Zhang M Y, et al. Effects of reduced and enhanced glycogen pools on salt-induced sucrose production in a sucrose-secreting strain of Synechococcus elongatus PCC 7942. Applied and Environmental Microbiology, 2018, 84(2): e02023-e02017.
|
[44] |
Abramson B W, Lensmire J, Lin Y T, et al. Redirecting carbon to bioproduction via a growth arrest switch in a sucrose-secreting cyanobacterium. Algal Research, 2018, 33: 248-255.
doi: 10.1016/j.algal.2018.05.013
|
[45] |
Lin P C, Zhang F Z, Pakrasi H B. Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973. Scientific Reports, 2020, 10: 390.
doi: 10.1038/s41598-019-57319-5
|
[46] |
Qiao Y, Wang W H, Lu X F. Engineering cyanobacteria as cell factories for direct trehalose production from CO2. Metabolic Engineering, 2020, 62: 161-171.
doi: S1096-7176(20)30134-8
pmid: 32898716
|
[47] |
Liang Y J, Zhang M Y, Wang M, et al. Freshwater cyanobacterium Synechococcus elongatus PCC 7942 adapts to an environment with salt stress via ion-induced enzymatic balance of compatible solutes. Applied and Environmental Microbiology, 2020, 86(7): e02904-e02919.
|
[48] |
van der Woude A D, Perez Gallego R, Vreugdenhil A, et al. Genetic engineering of Synechocystis PCC 6803 for the photoautotrophic production of the sweetener erythritol. Microbial Cell Factories, 2016, 15: 60.
doi: 10.1186/s12934-016-0458-y
|
[49] |
Wu W Y, Du W, Gallego R P, et al. Using osmotic stress to stabilize mannitol production in Synechocystis sp. PCC6803. Biotechnology for Biofuels, 2020, 13: 117.
doi: 10.1186/s13068-020-01755-3
|
[50] |
Niederholtmeyer H, Wolfstädter B T, Savage D F, et al. Engineering cyanobacteria to synthesize and export hydrophilic products. Applied and Environmental Microbiology, 2010, 76(11): 3462-3466.
doi: 10.1128/AEM.00202-10
pmid: 20363793
|
[51] |
Elbein A D, Pan Y T, Pastuszak I, et al. New insights on trehalose: a multifunctional molecule. Glycobiology, 2003, 13(4): 17R-27R.
doi: 10.1093/glycob/cwg047
pmid: 12626396
|
[52] |
Park J C, Jeong H, Kim Y, et al. Trehalose biosynthetic gene otsB of Corynebacterium glutamicum is regulated by whcE in response to oxidative stress. Microbiology (Reading, England), 2022, 168(1): 2022Jan; 168(1).
|
[53] |
Jacobsen J H, Frigaard N U. Engineering of photosynthetic mannitol biosynthesis from CO2 in a cyanobacterium. Metabolic Engineering, 2014, 21: 60-70.
doi: 10.1016/j.ymben.2013.11.004
pmid: 24269997
|
[54] |
Velmurugan R, Incharoensakd A, et al. Disruption of polyhydroxybutyrate synthesis redirects carbon flow towards glycogen synthesis in Synechocystis sp. PCC 6803 overexpressing glgC/glgA. Plant & Cell Physiology, 2018, 59(10): 2020-2029.
|
[55] |
Shimakawa G, Hasunuma T, Kondo A, et al. Respiration accumulates Calvin cycle intermediates for the rapid start of photosynthesis in Synechocystis sp. PCC6803. Bioscience Biotechnology and Biochemistry, 2014, 78(12): 1997-2007.
doi: 10.1080/09168451.2014.943648
|
[56] |
Comer A D, Abraham J P, Steiner A J, et al. Enhancing photosynthetic production of glycogen-rich biomass for use as a fermentation feedstock. Frontiers in Energy Research 2020, 8: 93.
doi: 10.3389/fenrg.2020.00093
|
[57] |
Muro-Pastor M I, Cutillas-Farray A, Perez-Rodriguez L, et al. CfrA, a novel carbon flow regulator, adapts carbon metabolism to nitrogen deficiency in cyanobacteria. Plant Physiology, 2020, 184(4): 1792-1810.
doi: 10.1104/pp.20.00802
pmid: 32900980
|
|
Viewed |
|
|
|
Full text
|
|
|
|
|
Abstract
|
|
|
|
|
Cited |
|
|
|
|
|
Shared |
|
|
|
|
|
Discussed |
|
|
|
|