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一株高产淀粉绿藻——标志链带藻在废水中的培养及对氮磷的去除

周芷薇, 沈丹丹, 高保燕, 黄罗冬, 李爱芬, 张成武

周芷薇, 沈丹丹, 高保燕, 黄罗冬, 李爱芬, 张成武. 一株高产淀粉绿藻——标志链带藻在废水中的培养及对氮磷的去除[J]. 植物科学学报, 2016, 34(3): 446-459. DOI: 10.11913/PSJ.2095-0837.2016.30446
引用本文: 周芷薇, 沈丹丹, 高保燕, 黄罗冬, 李爱芬, 张成武. 一株高产淀粉绿藻——标志链带藻在废水中的培养及对氮磷的去除[J]. 植物科学学报, 2016, 34(3): 446-459. DOI: 10.11913/PSJ.2095-0837.2016.30446
ZHOU Zhi-Wei, SHEN Dan-Dan, GAO Bao-Yan, HUANG Luo-Dong, LI Ai-Fen, ZHANG Cheng-Wu. Cultivation of a Starch-rich Microalga Desmodesmus insignis in Dairy Wastewater and Removal of Nitrogen and Phosphorus[J]. Plant Science Journal, 2016, 34(3): 446-459. DOI: 10.11913/PSJ.2095-0837.2016.30446
Citation: ZHOU Zhi-Wei, SHEN Dan-Dan, GAO Bao-Yan, HUANG Luo-Dong, LI Ai-Fen, ZHANG Cheng-Wu. Cultivation of a Starch-rich Microalga Desmodesmus insignis in Dairy Wastewater and Removal of Nitrogen and Phosphorus[J]. Plant Science Journal, 2016, 34(3): 446-459. DOI: 10.11913/PSJ.2095-0837.2016.30446
周芷薇, 沈丹丹, 高保燕, 黄罗冬, 李爱芬, 张成武. 一株高产淀粉绿藻——标志链带藻在废水中的培养及对氮磷的去除[J]. 植物科学学报, 2016, 34(3): 446-459. CSTR: 32231.14.PSJ.2095-0837.2016.30446
引用本文: 周芷薇, 沈丹丹, 高保燕, 黄罗冬, 李爱芬, 张成武. 一株高产淀粉绿藻——标志链带藻在废水中的培养及对氮磷的去除[J]. 植物科学学报, 2016, 34(3): 446-459. CSTR: 32231.14.PSJ.2095-0837.2016.30446
ZHOU Zhi-Wei, SHEN Dan-Dan, GAO Bao-Yan, HUANG Luo-Dong, LI Ai-Fen, ZHANG Cheng-Wu. Cultivation of a Starch-rich Microalga Desmodesmus insignis in Dairy Wastewater and Removal of Nitrogen and Phosphorus[J]. Plant Science Journal, 2016, 34(3): 446-459. CSTR: 32231.14.PSJ.2095-0837.2016.30446
Citation: ZHOU Zhi-Wei, SHEN Dan-Dan, GAO Bao-Yan, HUANG Luo-Dong, LI Ai-Fen, ZHANG Cheng-Wu. Cultivation of a Starch-rich Microalga Desmodesmus insignis in Dairy Wastewater and Removal of Nitrogen and Phosphorus[J]. Plant Science Journal, 2016, 34(3): 446-459. CSTR: 32231.14.PSJ.2095-0837.2016.30446

一株高产淀粉绿藻——标志链带藻在废水中的培养及对氮磷的去除

基金项目: 

国家高技术研究发展计划"863"项目(2013AA065805)

国家自然科学基金项目(31170337)

广东省低碳专项(2011-051)

珠海市科技重大项目(PB20041018)

珠海市科技攻关项目(PC20081008)。

详细信息
    作者简介:

    周芷薇(1991-),女,硕士研究生,研究方向为微藻生物技术(E-mail:air9137@126.com);沈丹丹(1984-),女,硕士研究生,研究方向为微藻生物技术(E-mail:shendan0375@163.com)。共同第一作者。

    通讯作者:

    张成武(1963-),男,博士,教授,博士生导师,主要从事微藻生物能源技术方面的研究(E-mail:tzhangcw@jnu.edu.cn)。

  • 中图分类号: TK6;Q949.21

Cultivation of a Starch-rich Microalga Desmodesmus insignis in Dairy Wastewater and Removal of Nitrogen and Phosphorus

Funds: 

This work was supported by grants from the National High-Tech R&D Program (863 Program, 2013AA065805), National Natural Science Foundation of China (31170337), Guangdong Low-Carbon Program (2011-051), Zhuhai Major Projects of Science and Technology (PB20041018), and Key Project of Science and Technology of Zhuhai (PC20081008).

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  • 摘要: 为了研究标志链带藻(Desmodesmus insignis strain JNU24)在不同NaNO3浓度和不同废水浓度培养下的生长与代谢产物积累状况,评估标志链带藻对废水的处理能力,本研究利用柱状光反应器对标志链带藻进行培养,分别对4种NaNO3浓度的BG-11培养基和4种废水浓度培养下藻细胞的生物量、蛋白质含量、碳水化合物含量和淀粉含量进行了测定。结果显示,在BG-11培养基中,氮浓度为9.0mmol/L时,藻细胞生物质浓度最高,达6.23g/L;在废水培养下,未稀释的原废水实验组,其藻细胞生物质浓度最高,达10.31g/L;75%废水培养下,藻细胞的淀粉含量最高(达50.9%),单位体积藻细胞淀粉含量和产率分别为4.86g/L和405mg·L-1·d-1,且显著高于不同浓度NaNO3的BG-11培养基组。本研究还测定了标志链带藻对废水中氮、磷的去除效率,结果显示不同浓度废水培养下,氮、磷的去除效率最高可达90.8%和98.7%。基于柱状反应器中的最佳培养效果,以9.0mmol/LNaNO3的BG-11培养基和75%废水于3.0cm光径平板光生物反应器中进行室内扩大培养,结果显示在75%废水培养下,藻细胞生物质浓度达9.75g/L,淀粉单位体积含量和产率分别达到4.75g/L和230mg·L-1·d-1,且为9.0mmol/LNaNO3的BG-11培养基培养的3倍。通过沉降特性分析发现,藻细胞收获90min后均完全沉降,具有较强的沉降性能。本研究标志链带藻能够耐受废水中较高的氮、磷浓度,且对废水中氮、磷有显著的去除作用;该藻能利用废水中的营养成分积累较高的生物量和淀粉含量并且藻细胞能快速沉降,具有极高的经济价值和应用价值,是一株淀粉生产能力较高和废水处理能力较强的极具开发潜力的藻株。
    Abstract: Desmodesmus insignis strain JNU24 was cultivated in BG-11 medium containing four different initial NaNO3 concentrations and dairy wastewater (DWW) diluted into four concentrations to compare its growth, starch production performance, and nitrogen and phosphorus removal capacity in DWW. Results indicated that the optimum nitrate concentrations and DWW concentration for growth were 9.0 mmol/L and 100%, respectively, in which biomass achieved was 6.23 g/L and 10.31 g/L, respectively. Compared with the BG-11 group, however, D. insignis showed a greater ability to grow and accumulate starch when cultivated with 75% DWW, in which the starch content, volumetric starch content, and productivity reached 50.9%, 4.86 g/L, and 405 mg·L-1·d-1 respectively. In addition, D. insignis removed 90.8% of nitrogen and 98.7% of phosphorus from DWW. Indoor scaled-up cultivation of D. insignis was carried out in vertical flat-plate glass photobioreactors based on optimum concentrations of BG-11 and DWW. The maximum biomass concentration, volumetric starch content, and productivity of D. insignis were obtained under 75% DWW, reaching 9.75 g/L, 4.75 g/L, and 230 mg·L-1·d-1, respectively, which were approximately two times greater than those obtained in the BG-11 group. These results showed that D. insignis could tolerant high nitrate concentrations in DWW, and could be applied on a large scale with cheap media. The D. insignis cells exhibited outstanding settling capacity, as inferred from their ability to settle within 90 min in 75% DWW after stopping aeration. In conclusion, D. insignis is a microalga that has the potential to produce starch and purify wastewater.
  • [1]

    Singh A, Nigam PS, Murphy JD. Renewable fuels from algae: An answer to debatable land based fuels[J]. Bioresource Technol, 2011, 102: 10-16.

    [2]

    Harun R, Danquah MK, Forde GM. Microalgal biomass as a fermentation feedstock for bioethanol production[J]. J Chem Technol Biot, 2010, 85(2): 199-203.

    [3]

    Kim MS, Baek JS, Yun YS, Sim SJ, Park S, Kim SC. Hydrogen production from Chlamydomonas reinhardtii biomass using a two-step conversion process: Anaerobic conversion and photosynthetic fermentation[J]. Int J Hydrogen Energ, 2006, 31: 812 -816.

    [4]

    Rodjaroen S, Juntawong N, Mahakhant A, Miyamoto K. High biomass production and starch accumulation in native green algal strains and cyanobacterial strains of Thailand[J]. Nat Sci,2007, 41: 570-575.

    [5]

    Nguyen MT, Choi SP, Lee J, H, Sim SJ. Hydrothermal acid pretreatment of Chlamydomonas reinhardtii biomass for ethanol production[J]. J Microbiol Biotechn, 2009, 19(2): 161-166.

    [6]

    Ueno Y, Kurano N, Miyachi S. Ethanol production by dark fermentation in the marine green alga, Chlorococcum littorale[J]. J Ferment Bioeng, 1998, 86(1): 38-43.

    [7]

    Ueda R, Hirayama S, Sugata K, Nakayama H. Process for the production of ethanol from microalgae. US Patent, 5578472.1996-11-26.

    [8]

    Subhadra B, Edwards M. An integrated renewable energy park approach for algal biofuel production in United States[J]. Energ Policy,2010, 38(9): 4897-4902.

    [9]

    Packer M. Algal capture of carbon dioxide; biomass ge-neration as a tool for greenhouse gas mitigation with refe-rence to New Zealand energy strategy and policy[J]. Energ Policy, 2009, 37(9): 3428-3437.

    [10]

    Ignacio MG. Microalgae immobilization: current techniques and uses[J]. Bioresource Technol, 2008, 99(10): 3949-3964.

    [11]

    Mallick N. Biotechnological potential of immobilized algae for wastewater N, P and metal removal: a review [J]. Biometals,2002, 15: 377-390.

    [12]

    Li X, Hu HY, Gan K, Ying-xue S. Effects of different nitrogen and phosphorus concentrations on the growth, nutrient uptake, and lipid accumulation of a freshwater microalga Scenedesmus sp.[J]. Bioresource Technol, 2010, 101: 5494-5500.

    [13]

    Meyen FJF. Beobachtungen über Einige Niedere Algenformen[M]. Nova Acta: Phys.-med. Acad. Caesar. Leop. Carol,1829,14: 769-778.

    [14]

    Chodat R. Scenedesmus[J]. Zeitschrift für Hydrologie, 1926, 3(3-4): 71-258.

    [15]

    An SS, Friedl T, Hegewald E. Phylogenetic relationships of Scenedesmus and Scenedesmus-like coccoid green algae as inferred from ITS-2 rDNA sequence comparisons[J]. Plant Biol, 1999, 1(4): 418-428.

    [16]

    Groben R, John U, Eller G, Lange M, Medlin LK. Using fluorescently-labelled rRNA probes for hierarchical estimation of phytoplankton diversity-a mini-review[J]. Nova Hedwigia, 2004, 79(1-2): 313-320.

    [17]

    Johnson JL, Fawley MW, Fawley KP. The diversity of Scenedesmus and Desmodesmus (Chlorophyceae) in Itasca State Park, Minnesota, USA[J]. Phycologia, 2007, 46(2): 214-229.

    [18]

    Rawat I, Kumar RR, Mutanda T, Bux F. Dual role of microalgae: Phycoremediation of domestic wastewater and biomass production for sustainable biofuels production[J]. Applied Energy, 2011, 88(10): 3411-3424.

    [19]

    Dubois M, Gilles KA, Hamilton JK, Rebers P, Smith F. Colorimetric method for determination of sugars and rela-ted substances[J]. Anal Chem, 1956, 28 (3): 350-356.

    [20]

    Mccready RM, Guggolz J, Silviera V, Owens HS. Determination of starch and amylose in vegetables[J]. Anal Chem,1950, 22(9): 1156-1158.

    [21]

    John DM. Phylum Chlorophyta (Green Algae)[M]//John DM, Whitton BA, Brook AJ eds. The Freshwater Algal Flora of The British Isles. 2nd ed. Cambridge: Cambridge University Press, 2011:440-443.

    [22]

    Mutanda T, Ramesh D, Karthikeyan S, et al. Bioprospec-ting for hyper-lipid producing microalgal strains for sustai-nable biofuel production[J]. Bioresource Technol, 2011,1(102): 57-70.

    [23]

    Pittman JK, Dean AP, Osundeko O. The potential of sustainable algal biofuel production using wastewater resources[J].Bioresource Technol, 2011,1(102): 17-25.

    [24]

    Brányiková I, Maršálková B, Doucha J, Brányik T, Bišová K, Zachleder V, Vítová M. Microalgae-novel highly efficient starch producers[J]. Biotechnol Bioeng, 2011, 108(4): 766-776.

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出版历程
  • 收稿日期:  2015-11-24
  • 修回日期:  2016-01-12
  • 网络出版日期:  2022-10-31
  • 发布日期:  2016-06-27

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