Indian Journal of Science and Technology

References

1. Chew KW, Yap JY, Show PL, Suan NH, Juan JC, Ling TC, et al. Microalgae biorefinery: High value products perspectives. Bioresource Technology. 2017;229:53–62. Available from: https://dx.doi.org/10.1016/j.biortech.2017.01.006
2. Fazal T, Mushtaq A, Rehman F, Khan AU, Rashid N, Farooq W, et al. Bioremediation of textile wastewater and successive biodiesel production using microalgae. Renewable and Sustainable Energy Reviews. 2018;82:3107–3126. Available from: https://dx.doi.org/10.1016/j.rser.2017.10.029
3. Nzayisenga JC, Eriksson K, Sellstedt A. Mixotrophic and heterotrophic production of lipids and carbohydrates by a locally isolated microalga using wastewater as a growth medium. Bioresource Technology. 2018;257:260–265. Available from: https://dx.doi.org/10.1016/j.biortech.2018.02.085
4. Wu JY, Lay CH, Chen CC, Wu SY. Lipid accumulating microalgae cultivation in textile wastewater: Environmental parameters optimization. Journal of the Taiwan Institute of Chemical Engineers. 2017;79:1–6. Available from: https://dx.doi.org/10.1016/j.jtice.2017.02.017
5. Singh SK, Sundaram S, Sinha S, Rahman MA, Kapur S. Recent advances in CO2uptake and fixation mechanism of cyanobacteria and microalgae. Critical Reviews in Environmental Science and Technology. 2016;46(16):1297–1323. Available from: https://dx.doi.org/10.1080/10643389.2016.1217911
6. Rashid N, Selvaratnam T, Park WK. Resource recovery from waste streams using microalgae: opportunities and threats. In: Microalgae Cultivation for Biofuels Production. (pp. 337-351) Elsevier Inc: United State. 2020.
7. Cheng P, Wang J, Liu T. Effects of nitrogen source and nitrogen supply model on the growth and hydrocarbon accumulation of immobilized biofilm cultivation of B. braunii. Bioresource Technology. 2014;166:527–533. Available from: https://dx.doi.org/10.1016/j.biortech.2014.05.045
8. Fakhry EM, Maghraby DME. Lipid accumulation in response to nitrogen limitation and variation of temperature in Nannochloropsis salina. Botanical Studies. 2015;56(1):6–13. Available from: https://dx.doi.org/10.1186/s40529-015-0085-7
9. Jerez CG, Malapascua JR, Sergejevová M, Figueroa FL, Masojídek J. Effect of Nutrient Starvation under High Irradiance on Lipid and Starch Accumulation in Chlorella fusca (Chlorophyta) Marine Biotechnology. 2016;18(1):24–36. Available from: https://dx.doi.org/10.1007/s10126-015-9664-6
10. Zhu S, Huang W, Xu J, Wang Z, Xu J, Yuan Z. Metabolic changes of starch and lipid triggered by nitrogen starvation in the microalga Chlorella zofingiensis. Bioresource Technology. 2014;152:292–298. Available from: https://dx.doi.org/10.1016/j.biortech.2013.10.092
11. Liu J, Mukherjee J, Hawkes JJ, Wilkinson SJ. Optimization of lipid production for algal biodiesel in nitrogen stressed cells ofDunaliella salinausing FTIR analysis. Journal of Chemical Technology & Biotechnology. 2013;88(10):1807–1814. Available from: https://dx.doi.org/10.1002/jctb.4027
12. Li T, Xu J, Gao B, Xiang W, Li A, Zhang C. Morphology, growth, biochemical composition and photosynthetic performance of Chlorella vulgaris (Trebouxiophyceae) under low and high nitrogen supplies. Algal Research. 2016;16:481–491. Available from: https://dx.doi.org/10.1016/j.algal.2016.04.008
13. Kim G, Bae J, Lee K. Nitrate repletion strategy for enhancing lipid production from marine microalga Tetraselmis sp. Bioresource Technology. 2016;205:274–279. Available from: https://dx.doi.org/10.1016/j.biortech.2016.01.045
14. Berges JA, Charlebois DO, Mauzerall DC, Falkowski PG. Differential Effects of Nitrogen Limitation on Photosynthetic Efficiency of Photosystems I and II in Microalgae. Plant Physiology. 1996;110(2):689–696. Available from: https://dx.doi.org/10.1104/pp.110.2.689
15. Zhang YM, Chen H, He CL, Wang Q. Nitrogen Starvation Induced Oxidative Stress in an Oil-Producing Green Alga Chlorella sorokiniana C3. PLoS ONE. 2013;8(7):e69225. Available from: https://dx.doi.org/10.1371/journal.pone.0069225
16. Safdar W, Shamoon M, Zan X, Haider J, Sharif HR, Shoaib M, et al. Growth kinetics, fatty acid composition and metabolic activity changes of Crypthecodinium cohnii under different nitrogen source and concentration. AMB Express. 2017;7:85–99. Available from: https://dx.doi.org/10.1186/s13568-017-0384-3
17. Hu Q, Sommerfeld M, Jarvis E, Ghirardi M, Posewitz M, Seibert M, et al. Microalgal triacylglycerols as feedstocks for biofuel production: perspectives and advances. The Plant Journal. 2008;54(4):621–639. Available from: https://dx.doi.org/10.1111/j.1365-313x.2008.03492.x
18. Yang ZK, Zheng JW, Niu YF, Yang WD, Liu JS, Li HY. Systems-level analysis of the metabolic responses of the diatomPhaeodactylum tricornutumto phosphorus stress. Environmental Microbiology. 2014;16(6):1793–1807. Available from: https://dx.doi.org/10.1111/1462-2920.12411
19. Necla Altın T, Kutluk B, Uyar N, Kapucu. Effect of different nitrogen sources on the growth and lipid accumulation of Chlorella variabilis. Journal of Applied Biological Sciences. 2018;12:38–40.
20. Kim G, Mujtaba G, Lee K. Effects of nitrogen sources on cell growth and biochemical composition of marine chlorophyte Tetraselmis sp. for lipid production. ALGAE. 2016;31(3):257–266. Available from: https://dx.doi.org/10.4490/algae.2016.31.8.18
21. Shrivastav A, Mishra SK, Suh WI, Farooq W, Moon M, Kim TH, et al. Characterization of newly isolated oleaginous microalga Monoraphidium sp. for lipid production under different conditions. Algal Research. 2015;12:289–294. Available from: https://dx.doi.org/10.1016/j.algal.2015.08.015
22. Li Y, Horsman M, Wang B, Wu N, Lan CQ. Effects of nitrogen sources on cell growth and lipid accumulation of green alga Neochloris oleoabundans. Applied Microbiology and Biotechnology. 2008;81(4):629–636. Available from: https://dx.doi.org/10.1007/s00253-008-1681-1
23. Wu LF, Chen PC, Lee CM. The effects of nitrogen sources and temperature on cell growth and lipid accumulation of microalgae. International Biodeterioration & Biodegradation. 2013;85:506–510. Available from: https://dx.doi.org/10.1016/j.ibiod.2013.05.016
24. Zhan J, Hong Y, Hu H. Effects of Nitrogen Sources and C/N Ratios on the Lipid-Producing Potential of Chlorella sp. HQ. Journal of Microbiology and Biotechnology. 2016;26(7):1290–1302. Available from: https://dx.doi.org/10.4014/jmb.1512.12074
25. Ramanna L, Guldheismail A. Rawat Faizal Bux. The optimization of biomass and lipid yields of Chlorella sorokiniana when using wastewater supplemented with different nitrogen sources. Bioresource Technolology. 2014;168:127–135.
26. Sibi G. Cultural Conditions and Nutrient Composition as Effective Inducers for Biomass and Lipid Production in Fresh Water Microalgae. Research Journal of Environmental Toxicology. 2015;9(4):168–178. Available from: https://dx.doi.org/10.3923/rjet.2015.168.178
27. Zhu L, Li S, Hu T, Nugroho YK, Yin Z, Hu D, et al. Effects of nitrogen source heterogeneity on nutrient removal and biodiesel production of mono- and mix-cultured microalgae. Energy Conversion and Management. 2019;201:112144. Available from: https://dx.doi.org/10.1016/j.enconman.2019.112144
28. Campos H, Boeing WJ, Dungan BN. Tanner Schaub Cultivating the marine microalga Nannochloropsis salina under various nitrogen sources: Effect on biovolume yields, lipid content and composition, and invasive organisms. Biomass Bioenergy. 2014;66:301–307.
29. Miranda CT, Lima DVNd, Atella GC, Aguiar PFd, Azevedo SMFO. Optimization of Nitrogen, Phosphorus and Salt for Lipid Accumulation of Microalgae: Towards the Viability of Microalgae Biodiesel. Natural Science. 2016;08(12):557–573. Available from: https://dx.doi.org/10.4236/ns.2016.812055
30. Bajwa K, Narsi R, Bishnoi A, Kirrollia, Selvan ST. A new lipid rich microalgal sp Scenedesmus dimorphus isolated: Nile red staining and effect of carbon, nitrogen sources on its physio-biochemical components. European Journal of Sustainable Development Research. 2018;2:143–152.
31. Zhao XC, Tan XB, Yang LB, Liao JY, Li XY. Cultivation of Chlorella pyrenoidosa in anaerobic wastewater: The coupled effects of ammonium, temperature and pH conditions on lipids compositions. Bioresource Technology. 2019;284:90–97. Available from: https://dx.doi.org/10.1016/j.biortech.2019.03.117
32. Wang X, Shen Z, Miao X. Nitrogen and hydrophosphate affects glycolipids composition in microalgae. Scientific Reports. 2016;6(1):1–9. Available from: https://dx.doi.org/10.1038/srep30145
33. Gifuni I, Olivieri G, Pollio A, Marzocchella A. Identification of an industrial microalgal strain for starch production in biorefinery context: The effect of nitrogen and carbon concentration on starch accumulation. New Biotechnology. 2018;41:46–54. doi: 10.1016/j.nbt.2017.12.003
34. Gupta N, Khare P, Singh DP. Nitrogen-dependent metabolic regulation of lipid production in microalga Scenedesmus vacuolatus. Ecotoxicology and Environmental Safety. 2019;174:706–713. Available from: https://dx.doi.org/10.1016/j.ecoenv.2019.03.035
35. Wang S, Zheng L, Han X, Yang B, Li J, Sun C. Lipid accumulation and CO2 utilization of two marine oil-rich microalgal strains in response to CO2 aeration. Acta Oceanologica Sinica. 2018;37(2):119–126. Available from: https://dx.doi.org/10.1007/s13131-018-1171-y
36. Liu X, Wang K, Wang J, Zuo J, Peng F, Wu J, et al. Carbon dioxide fixation coupled with ammonium uptake by immobilized Scenedesmus obliquus and its potential for protein production. Bioresource Technology. 2019;289:121685. Available from: https://dx.doi.org/10.1016/j.biortech.2019.121685
37. Patil L, Kaliwal B. Effect of CO2 Concentration on Growth and Biochemical Composition of Newly Isolated Indigenous Microalga Scenedesmus bajacalifornicus BBKLP-07. Applied Biochemistry and Biotechnology. 2017;182(1):335–348. Available from: https://dx.doi.org/10.1007/s12010-016-2330-2
38. Khairy HM, Shaltout NA, El-Naggar MF, El-Naggar NA. Impact of elevated CO2 concentrations on the growth and ultrastructure of non-calcifying marine diatom (Chaetoceros gracilis F.Schütt) Elsevier BV. 2014. Available from: https://dx.doi.org/10.1016/j.ejar.2014.08.002
39. Singh SK, Sundaram S, Sinha S, Rahman MA, Kapur S. Recent advances in CO2uptake and fixation mechanism of cyanobacteria and microalgae. Critical Reviews in Environmental Science and Technology. 2016;46(16):1297–1323. Available from: https://dx.doi.org/10.1080/10643389.2016.1217911
40. Mondal M, Khanra S, Tiwari ON, Gayen K, Halder GN. Role of carbonic anhydrase on the way to biological carbon capture through microalgae-A mini review. Environmental Progress & Sustainable Energy. 2016;35(6):1605–1615. Available from: https://dx.doi.org/10.1002/ep.12394
41. Ghosh A, Kiran B. Carbon Concentration in Algae: Reducing CO 2 From Exhaust Gas. Trends in Biotechnology. 2017;35(9):806–808. Available from: https://dx.doi.org/10.1016/j.tibtech.2017.05.003
42. Liran O, Shemesh E, Tchernov D. Investigation into the CO2 concentrating step rates within the carbon concentrating mechanism of Synechocystis sp. PCC6803 at various pH and light intensities reveal novel mechanistic properties. Algal Research. 2018;33:419–429. Available from: https://dx.doi.org/10.1016/j.algal.2018.06.020
43. Baba M, Shiraiw Y. High-CO2 response mechanisms in microalgae. Advances in Photosynthesis-Fundamental Aspects. N.Najafpour. 2012;p. 299–320.
44. Swarnalatha GV, Hegde NS, Chauhan VS, Sarada R. The effect of carbon dioxide rich environment on carbonic anhydrase activity, growth and metabolite production in indigenous freshwater microalgae. Algal Research. 2015;9:151–159. Available from: https://dx.doi.org/10.1016/j.algal.2015.02.014
45. Patel AK, Joun JM, Hong ME, Sim SJ. Effect of light conditions on mixotrophic cultivation of green microalgae. Bioresource Technology. 2019;282:245–253. Available from: https://dx.doi.org/10.1016/j.biortech.2019.03.024
46. Qiao H, Wang G. Effect of carbon source on growth and lipid accumulation in Chlorella sorokiniana GXNN01. Chinese Journal of Oceanology and Limnology. 2009;27(4):762–768. Available from: https://dx.doi.org/10.1007/s00343-009-9216-x
47. Velu P, Peter MJ, Sanniyasi E. Effect of Various Carbon Sources on Biochemical Production in Marine Microalgae Nannochloropsis salina, Dunaliella tertiolecta (Chlorophyceae) and Tetraselmis suecica (Chlorodendrophyceae) International Journal of Current Microbiology and Applied Sciences. 2015;4:207–215.
48. Bhatnagar A, Chinnasamy S, Singh M, Das KC. Renewable biomass production by mixotrophic algae in the presence of various carbon sources and wastewaters. Applied Energy. 2011;88(10):3425–3431. Available from: https://dx.doi.org/10.1016/j.apenergy.2010.12.064
49. Danesh A, Zilouei H, Farhadian O. The effect of glycerol and carbonate on the growth and lipid production of Isochrysis galbana under different cultivation modes. Journal of Applied Phycology. 2019;31(6):3411–3420. Available from: https://dx.doi.org/10.1007/s10811-019-01888-5
50. Zhang W, Zhang P, Sun H, Chen M, Lu S, Li P. Effects of various organic carbon sources on the growth and biochemical composition of Chlorella pyrenoidosa. Bioresource Technology. 2014;173:52–58. Available from: https://dx.doi.org/10.1016/j.biortech.2014.09.084
51. Gim GH, Kim JK, Kim HS, Kathiravan MN, Yang H, Jeong SH, et al. Comparison of biomass production and total lipid content of freshwater green microalgae cultivated under various culture conditions. Bioprocess and Biosystems Engineering. 2014;37(2):99–106. Available from: https://dx.doi.org/10.1007/s00449-013-0920-8
52. Pang N, Gu X, Fu X, Chen S. Effects of gluconate on biomass improvement and light stress tolerance of Haematococcus pluvialis in mixotrophic culture. Algal Research. 2019;43:101647. Available from: https://dx.doi.org/10.1016/j.algal.2019.101647
53. Bashir KMI, Mansoor S, Kim NR, Grohmann FR, Shah AA, Cho MG. Effect of organic carbon sources and environmental factors on cell growth and lipid content of Pavlova lutheri. Annals of Microbiology. 2019;69(4):353–368. Available from: https://dx.doi.org/10.1007/s13213-018-1423-2
54. Sharma AK, Sahoo PK, Singhal S, Patel A. Impact of various media and organic carbon sources on biofuel production potential from Chlorella spp. 3 Biotech. 2016;6(2). Available from: https://dx.doi.org/10.1007/s13205-016-0434-6
55. Tanner W. The chlorella hexose/H+-symporters. International Review of Cytology. 2000;200.
56. Zheng Y, Yu X, Li T, Xiong X, Chen S. Induction of D-xylose uptake and expression of NAD(P)H-linked xylose reductase and NADP+-linked xylitol dehydrogenase in the oleaginous microalga Chlorella sorokiniana. Biotechnology for Biofuels. 2014;7.
57. Lin TS, Wu JY. Effect of carbon sources on growth and lipid accumulation of newly isolated microalgae cultured under mixotrophic condition. Bioresource Technology. 2015;184:100–107. Available from: https://dx.doi.org/10.1016/j.biortech.2014.11.005
58. Chai S, Shi J, Huang T, Guo Y, Wei J, Guo M, et al. Characterization of Chlorella sorokiniana growth properties in monosaccharide-supplemented batch culture. PLOS ONE. 2018;13(7):e0199873. Available from: https://dx.doi.org/10.1371/journal.pone.0199873
59. Xie M, Qiu Y, Song C, Qi Y, Li Y, Kitamura Y. Optimization of Chlorella sorokiniana cultivation condition for simultaneous enhanced biomass and lipid production via CO 2 fixation. Bioresource Technology Reports. 2018;2:15–20. Available from: https://dx.doi.org/10.1016/j.biteb.2018.03.006
60. Zhang L, Wang YZ, Wang S, Ding K. Effect of carbon dioxide on biomass and lipid production of Chlorella pyrenoidosa in a membrane bioreactor with gas-liquid separation. Algal Research. 2018;31:70–76. Available from: https://dx.doi.org/10.1016/j.algal.2018.01.014
61. Huang YT, Su CP. High lipid content and productivity of microalgae cultivating under elevated carbon dioxide. International Journal of Environmental Science and Technology. 2014;11(3):703–710. doi: 10.1007/s13762-013-0251-y
62. Artamonova EY, Vasskog T, Eilertsen HC. Lipid content and fatty acid composition of Porosira glacialis and Attheya longicornis in response to carbon dioxide (CO2) aeration. PLOS ONE. 2017;12(5):e0177703. Available from: https://dx.doi.org/10.1371/journal.pone.0177703
63. Ji MK, Yun HS, Hwang JH, Salama ES, Jeon BH, Choi J. Effect of flue gas CO2 on the growth, carbohydrate and fatty acid composition of a green microalga Scenedesmus obliquus for biofuel production. Environmental Technology. 2017;38(16):2085–2092. Available from: https://dx.doi.org/10.1080/09593330.2016.1246145
64. Vidyashankar S, Deviprasad K, Chauhan VS, Ravishankar GA, Sarada R. Selection and evaluation of CO2 tolerant indigenous microalga Scenedesmus dimorphus for unsaturated fatty acid rich lipid production under different culture conditions. Bioresource Technology. 2013;144:28–37. Available from: https://dx.doi.org/10.1016/j.biortech.2013.06.054
65. Yang Y, Gao K. Effects of CO2 concentrations on the freshwater microalgae, Chlamydomonas reinhardtii, Chlorella pyrenoidosa and Scenedesmus obliquus (Chlorophyta) Journal of Applied Phycology. 2003;15:379–389.
66. Sengmee D, Cheirsilp B, Suksaroge TT, Prasertsan P. Biophotolysis-based hydrogen and lipid production by oleaginous microalgae using crude glycerol as exogenous carbon source. International Journal of Hydrogen Energy. 2017;42(4):1970–1976. Available from: https://dx.doi.org/10.1016/j.ijhydene.2016.10.089
67. Chen YH, Walker TH. Biomass and lipid production of heterotrophic microalgae Chlorella protothecoides by using biodiesel-derived crude glycerol. Biotechnnology Letters. 1973;33.
68. Gim GH, Ryu J, Kim MJ, Kim PI, Kim SW. Effects of carbon source and light intensity on the growth and total lipid production of three microalgae under different culture conditions. Journal of Industrial Microbiology & Biotechnology. 2016;43(5):605–616. doi: 10.1007/s10295-016-1741-y
69. Ren HY, Liu BF, Ma C, Zhao L, Ren NQ. A new lipid-rich microalga Scenedesmus sp. strain R-16 isolated using Nile red staining: effects of carbon and nitrogen sources and initial pH on the biomass and lipid production. Biotechnology for Biofuels. 2013;6(1):143. Available from: https://dx.doi.org/10.1186/1754-6834-6-143
70. Patidar SK, Mitra M, George B, Soundarya R, Mishra S. Potential of Monoraphidium minutum for carbon sequestration and lipid production in response to varying growth mode. Bioresource Technology. 2014;172:32–40. Available from: https://dx.doi.org/10.1016/j.biortech.2014.08.070
71. He Y, Hong Y, Liu X, Zhang Q, Liu P, Wang S. Influences of carbon and nitrogen sources and metal ions on the heterotrophic culture of Scenedesmus sp. LX1. Environmental Science and Pollution Research. 2019;26:13381–13389. Available from: https://dx.doi.org/10.1007/s11356-019-04807-w
72. Song M, Pei H. The growth and lipid accumulation of Scenedesmus quadricauda during batch mixotrophic/heterotrophic cultivation using xylose as a carbon source. Bioresource Technology. 2018;263:525–531. Available from: https://dx.doi.org/10.1016/j.biortech.2018.05.020
73. Wan M, Liu P, Xia J, Rosenberg JN, Oyler GA, Betenbaugh MJ, et al. The effect of mixotrophy on microalgal growth, lipid content, and expression levels of three pathway genes in Chlorella sorokiniana. Applied Microbiology and Biotechnology. 2011;91(3):835–844. Available from: https://dx.doi.org/10.1007/s00253-011-3399-8
74. Ru F, Ying WH, Feng PG. A study on lipid production of the mixotrophic microalgae Phaeodactylum tricornutum on various carbon sources. African Journal of Microbiology Research. 2012;6.
75. Krzemińska I, Oleszek M. Glucose supplementation-induced changes in the Auxenochlorella protothecoides fatty acid composition suitable for biodiesel production. Bioresource Technology. 2016;218:1294–1297. Available from: https://dx.doi.org/10.1016/j.biortech.2016.07.104
76. Chou HH, Su HY, Song XD, Chow TJ, Chen CY, Chang JS, et al. Isolation and characterization of Chlorella sp. mutants with enhanced thermo- and CO2 tolerances for CO2 sequestration and utilization of flue gases. Biotechnology for Biofuels. 2019;12(1):251–265. Available from: https://dx.doi.org/10.1186/s13068-019-1590-9
77. Mohsenpour SF, Willoughby N. Effect of CO 2 aeration on cultivation of microalgae in luminescent photobioreactors. Biomass and Bioenergy. 2016;85:168–177. Available from: https://dx.doi.org/10.1016/j.biombioe.2015.12.002
78. Yu SJ, Hu H, Zheng H, Wang YQ, Pan SB, Zeng RJ. Effect of different phosphorus concentrations on biodiesel production from Isochrysis zhangjiangensis under nitrogen sufficiency or deprivation condition. Applied Microbiology and Biotechnology. 2019;103(12):5051–5059. Available from: https://dx.doi.org/10.1007/s00253-019-09814-y
79. El-Kassas HY. Growth and fatty acid profile of the marine microalga Picochlorum Sp. grown under nutrient stress conditions. The Egyptian Journal of Aquatic Research. 2013;39(4):233–239. doi: 10.1016/j.ejar.2013.12.007
80. Huang B, Marchand J, Thiriet-Rupert S, Carrier G, Saint-Jean B, Lukomska E, et al. Betaine lipid and neutral lipid production under nitrogen or phosphorus limitation in the marine microalga Tisochrysis lutea (Haptophyta) Algal Research. 2019;40:101506. Available from: https://dx.doi.org/10.1016/j.algal.2019.101506
81. Alipanah L, Winge P, Rohloff J, Najafi J, Brembu T, Bones AM. Molecular adaptations to phosphorus deprivation and comparison with nitrogen deprivation responses in the diatom Phaeodactylum tricornutum. PLOS ONE. 2018;13(2):e0193335. Available from: https://dx.doi.org/10.1371/journal.pone.0193335
82. Mühlroth A, Winge P, El Assimi A, Jouhet J, Maréchal E, Hohmann-Marriott MF, et al. Mechanisms of Phosphorus Acquisition and Lipid Class Remodeling under P Limitation in a Marine Microalga. Plant Physiology. 2017;175(4):1543–1559. doi: 10.1104/pp.17.00621
83. Liang K, Zhang Q, Gu M, Cong W. Effect of phosphorus on lipid accumulation in freshwater microalga Chlorella sp. Journal of Applied Phycology. 2013;25(1):311–318. Available from: https://dx.doi.org/10.1007/s10811-012-9865-6
84. Anne-Marie K, Yee W, Loh SH, Aziz A. Thye San Cha. Effects of excess and limited phosphate on biomass, lipid and fatty acid contents and the expression of four fatty acid desaturase genes in the tropical Selenastraceaen Messastrum gracile SE-MC4. Applied Biochemistry and Biotechology. 2019;p. 1–19.
85. Xin L, Huhong-Ying G, Ke. SunYing-xue. Effects of different nitrogen and phosphorus concentrations on the growth, nutrient uptake, and lipid accumulation of a freshwater microalga Scenedesmus sp. Bioresource Technology. 2010;101:5494–5500.
86. José P, Lovio-Fragoso C, Hayano-Kanashiro, José A. López-Elías. Effect of different phosphorus concentrations on growth and biochemical composition of Chaetoceros muelleri. Latin American Journal of Aquatic Research. 2019;47:361–366.
87. Roopnarain A, Gray VM, Sym SD. Phosphorus limitation and starvation effects on cell growth and lipid accumulation in Isochrysis galbana U4 for biodiesel production. Bioresource Technology. 2014;156:408–411. Available from: https://dx.doi.org/10.1016/j.biortech.2014.01.092
88. Li Q, Fu L, Wang Y, Zhou D, Rittmann BE. Excessive phosphorus caused inhibition and cell damage during heterotrophic growth of Chlorella regularis. Bioresource Technology. 2018;268:266–270. Available from: https://dx.doi.org/10.1016/j.biortech.2018.07.148
89. Wang X, Shen Z, Miao X. Nitrogen and hydrophosphate affects glycolipids composition in microalgae. Scientific Reports. 2016;6(1):1–9. Available from: https://dx.doi.org/10.1038/srep30145
90. Challagulla V, Fabbro L, Nayar S. Biomass, lipid productivity and fatty acid composition of fresh water microalga Rhopalosolen saccatus cultivated under phosphorous limited conditions. Algal Research. 2015;8:69–75. Available from: https://dx.doi.org/10.1016/j.algal.2015.01.010
91. Rasdi NW, Qin JG. Effect of N:P ratio on growth and chemical composition of Nannochloropsis oculata and Tisochrysis lutea. Journal of Applied Phycology. 2015;27(6):2221–2230. doi: 10.1007/s10811-014-0495-z
92. Su G, Jiao K, Li Z, Guo X, Chang J, Ndikubwimana T, et al. Phosphate limitation promotes unsaturated fatty acids and arachidonic acid biosynthesis by microalgae Porphyridium purpureum. Bioprocess and Biosystems Engineering. 2016;39(7):1129–1136. doi: 10.1007/s00449-016-1589-6
93. Influence of various concentrations of phosphorus on the antibacterial, antioxidant and bioactive components of green microalgae Scenedesmus obliquus. International Journal of Pharmacology. 2017;14:99–107.
94. Bulut Mutlu Y, Işık O, Uslu L, Koç K, Durmaz Y. The effects of nitrogen and phosphorus deficiencies and nitrite addition on the lipid content of Chlorella vulgaris (Chlorophyceae) African Journal of Biotechnology. 2011;10.
95. Fu L, Li Q, Yan G, Zhou D, Crittenden JC. Hormesis effects of phosphorus on the viability of Chlorella regularis cells under nitrogen limitation. Biotechnology for Biofuels. 2019;12(1):1–9. Available from: https://dx.doi.org/10.1186/s13068-019-1458-z
96. Cho HU, Kim YM, Choi YN, Xu X, Shin DY, Park JM. Effects of pH control and concentration on microbial oil production from Chlorella vulgaris cultivated in the effluent of a low-cost organic waste fermentation system producing volatile fatty acids. Bioresource Technology. 2015;184:245–250. Available from: https://dx.doi.org/10.1016/j.biortech.2014.09.069
97. Yang L, Tan X, Li D, Chu H, Zhou X, Zhang Y, et al. Nutrients removal and lipids production by Chlorella pyrenoidosa cultivation using anaerobic digested starch wastewater and alcohol wastewater. Bioresource Technology. 2015;181:54–61. Available from: https://dx.doi.org/10.1016/j.biortech.2015.01.043
98. Moreno-Garcia L, Gariépy Y, Barnabé S, Raghavan GSV. Effect of environmental factors on the biomass and lipid production of microalgae grown in wastewaters. Algal Research. 2019;41:101521. Available from: https://dx.doi.org/10.1016/j.algal.2019.101521
99. Lau KY, Pleissner D, Lin CSK. Recycling of food waste as nutrients in Chlorella vulgaris cultivation. Bioresource Technology. 2014;170:144–151. Available from: https://dx.doi.org/10.1016/j.biortech.2014.07.096
100. De˛bowski M, Rusanowska P, Zielin´ski M, Dudek M. Zdzisława Romanowska-Duda. Biomass production and nutrient removal by Chlorella vulgaris from anaerobic digestion effluents. Energies. 2018;11.
101. Ma M, Yuan D, He Y, Park M, Gong Y, Hu Q. Effective control of Poterioochromonas malhamensis in pilot-scale culture of Chlorella sorokiniana GT-1 by maintaining CO2-mediated low culture pH. Algal Research. 2017;26:436–444. Available from: https://dx.doi.org/10.1016/j.algal.2017.06.023
102. Narala RR, Garg S, Sharma KK, Thomas-Hall SR, Deme M, Li Y, et al. Comparison of Microalgae Cultivation in Photobioreactor, Open Raceway Pond, and a Two-Stage Hybrid System. Frontiers in Energy Research. 2016;4:1–10. Available from: https://dx.doi.org/10.3389/fenrg.2016.00029
103. Chen CY, Zhao XQ, Yen HW, Ho SH, Cheng CL, Lee DJ, et al. Microalgae-based carbohydrates for biofuel production. Biochemical Engineering Journal. 2013;78:1–10. Available from: https://dx.doi.org/10.1016/j.bej.2013.03.006
104. Grossmann L, Hinrichs J, Weiss J. Cultivation and downstream processing of microalgae and cyanobacteria to generate protein-based technofunctional food ingredients. Critical Reviews in Food Science and Nutrition. 2019;p. 1–29. Available from: https://dx.doi.org/10.1080/10408398.2019.1672137
105. Fernández MdlÁ, Boiteux J, Espino M, Gomez FJV, Silva MF. Natural deep eutectic solvents-mediated extractions: The way forward for sustainable analytical developments. Analytica Chimica Acta. 2018;1038:1–10. Available from: https://dx.doi.org/10.1016/j.aca.2018.07.059
106. Sicaire AG, Vian M, Fine F, Joffre F, Carré P, Tostain S, et al. Alternative Bio-Based Solvents for Extraction of Fat and Oils: Solubility Prediction, Global Yield, Extraction Kinetics, Chemical Composition and Cost of Manufacturing. International Journal of Molecular Sciences. 2015;16(12):8430–8453. doi: 10.3390/ijms16048430
107. Suzana Wahidin A, Idris. Sitti Raehanah Muhamad Shaleh. Ionic liquid as a promising biobased green solvent in combination with microwave irradiation for direct biodiesel production. Bioresource Technology. 2016;206:150–154.
108. Du Y, Schuur B, Kersten SRA, Brilman DWF. Opportunities for switchable solvents for lipid extraction from wet algal biomass: An energy evaluation. Algal Research. 2015;11:271–283. Available from: https://dx.doi.org/10.1016/j.algal.2015.07.004
109. Griffiths MJ, Dicks RG, Richardson C, Susan TL, Harrison. Advantages and challenges of microalgae as a source of oil for biodiesel. In: SM, MG., eds. Biodiesel - Feedstocks and Processing Technologies. (pp. 177-196) INTECH Open Access Publisher. 2011.
110. Camarena-Bernard C, Rout NP. Native Microalgae from Eutrophic Water: Potential for Wastewater Treatment, Low-Cost Biomass, and Lipid Production. Industrial Biotechnology. 2018;14(5):257–264. Available from: https://dx.doi.org/10.1089/ind.2018.0009
111. Massimi R, Kirkwood AE. Screening microalgae isolated from urban storm- and wastewater systems as feedstock for biofuel. PeerJ. 2016;4(9):e2396. doi: 10.7717/peerj.2396
112. Nesamma AA, Shaikh KM, Jutur PP. KS(HoMM., ed. Genetic engineering of microalgae for production of value-added ingredients. (pp. 405-414) Elsevier Inc. 2015.
113. Schüler LM, Schulze PSC, Pereira H, Barreira L, León R, Varela J. Trends and strategies to enhance triacylglycerols and high-value compounds in microalgae. Algal Research. 2017;25:263–273. doi: 10.1016/j.algal.2017.05.025
114. Chen CY, Kao AL, Tsai ZC, Chow TJ, Chang HY, Zhao XQ, et al. Expression of type 2 diacylglycerol acyltransferse geneDGTT1fromChlamydomonas reinhardtiienhances lipid production inScenedesmus obliquus. Biotechnology Journal. 2016;11(3):336–344. Available from: https://dx.doi.org/10.1002/biot.201500272
115. Kang NK, Kim EK, Sung M, Kim YU, Jeong B, Chang YK. Increased biomass and lipid production by continuous cultivation ofNannochloropsis salinatransformant overexpressing a bHLH transcription factor. Biotechnology and Bioengineering. 2019;116(3):555–568. Available from: https://dx.doi.org/10.1002/bit.26894
116. Chou HH, Su HY, Song XD, Chow TJ, Chen CY, Chang JS, et al. Isolation and characterization of Chlorella sp. mutants with enhanced thermo- and CO2 tolerances for CO2 sequestration and utilization of flue gases. Biotechnology for Biofuels. 2019;12(1):251. Available from: https://dx.doi.org/10.1186/s13068-019-1590-9
117. Chew KW, Chia SR, Show PL, Yap YJ, Ling TC, Chang JS. Effects of water culture medium, cultivation systems and growth modes for microalgae cultivation: A review. Journal of the Taiwan Institute of Chemical Engineers. 2018;91:332–344. doi: 10.1016/j.jtice.2018.05.039
118. Remmers IM, Hidalgo-Ulloa A, Brandt BP, Evers WAC, Wijffels RH, Lamers PP. Continuous versus batch production of lipids in the microalgae Acutodesmus obliquus. Bioresource Technology. 2017;244:1384–1392. Available from: https://dx.doi.org/10.1016/j.biortech.2017.04.093
119. Tan XB, Lam MK, Uemura Y, Lim JW, Wong CY, Ramli A, et al. Semi-continuous cultivation of Chlorella vulgaris using chicken compost as nutrients source: Growth optimization study and fatty acid composition analysis. Elsevier BV. 2018. doi: 10.1016/j.enconman.2018.03.020
120. Martín LA, Popovich CA, Martinez AM, María C, Damiani PI, Leonardi. Oil assessment of Halamphora coffeaeformis diatom growing in a hybrid two-stage system for biodiesel production. Renewable Energy. 2019;92:127–135.
121. Narala RR, Garg S, Sharma KK, Thomas-Hall SR, Deme M, Li Y, et al. Comparison of Microalgae Cultivation in Photobioreactor, Open Raceway Pond, and a Two-Stage Hybrid System. Frontiers in Energy Research. 2016;4(29):1–10. doi: 10.3389/fenrg.2016.00029
122. Álvarez-Díaz PD, Ruiz J, Arbib Z, Barragán J, Garrido-Pérez C, Perales JA. Lipid Production of Microalga Ankistrodesmus falcatus Increased by Nutrient and Light Starvation in a Two-Stage Cultivation Process. Applied Biochemistry and Biotechnology. 2014;174(4):1471–1483. Available from: https://dx.doi.org/10.1007/s12010-014-1126-5
123. Gorain PC, Bagchi SK, Mallick N. Effects of calcium, magnesium and sodium chloride in enhancing lipid accumulation in two green microalgae. Environmental Technology. 2013;34(13-14):1887–1894. Available from: https://dx.doi.org/10.1080/09593330.2013.812668
124. Kumar V, Kumar R, Rawat D, Nanda M. Synergistic dynamics of light, photoperiod and chemical stimulants influences biomass and lipid productivity in Chlorella singularis (UUIND5) for biodiesel production. Applied Biological Chemistry. 2018;61(1):7–13. Available from: https://dx.doi.org/10.1007/s13765-017-0332-6