Abstract
One of the biggest challenges in the coming years is to reduce the impact of chronic diseases. Unhealthy eating is an increasing problem and underlies much of the increase in mortality from chronic diseases that are occurring worldwide. Diets based on plant foods are strongly associated with reduced risks in major chronic diseases, but the constituents in plants that promote health have proved difficult to identify. Plant cells have been used, in the past two decades, as efficient host systems with great potential for the expression of foreign proteins and for the production of nonprotein bioactive small molecules. Till date, the systems implemented include a variety of approaches using whole plants, plant tissue cultures, and cell cultures for the synthesis of a myriad of compounds that include foreign protein expression for the production of antibodies and vaccines. Plant cells have also been used as bioreactors for the massive production on plant-derived bioactive small molecules which are important dietary components or used in the industry as pharmaceuticals, pesticides, flavors, and fragrances. Plant genetics and metabolic engineering can be used to make foods that differ only in their content of specific phytonutrients.
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References
Allwood JW, Parker D, Beckmann M, Draper J, Goodacre R (2012) Fourier transform ion cyclotron resonance mass spectrometry for plant metabolite and metabolite identification. Methods Mol Biol 860:157–175
Aversano R, Savarese S, De Nova JM, Frusciante L, Punzo M, Carputo D (2009) Genetic stability at nuclear and plastid level of Solanum species and hybrids. Euphytica 165:353–361
Bairu MW, Aremu OD, Van Staden J (2011) Somaclonal variation in plants: causes and detection methods. Plant Growth Regul 63:147–173
Bajaj YPS (1990) Somaclonal variation-origin, induction, cryopreservation, and implication in plant breeding. In: Bajaj YPS (ed) Biotechnology in agriculture and forestry II. Somaclonal variation in crop improvement. Springer, Berlin pp 3–35
Ballester AR, Molthoff J, de Vos R, Hekert BT, Orzaez D, Fernández-Moreno JP, Tripodi P, Grandillo S, Martin C, Heldens J, Ykema N, Granell A, Bovy A (2010) Biochemical and molecular analysis of pink tomatoes: deregulated expression of the gene encoding transcription factor SlMYB12 leads to pink tomato fruit color. Plant Physiol 152:71–84
Barampuram S, Zhang ZJ (2011) Recent advances in plant transformation. In: Birchler JAA (ed) Plant chromosome engineering: methods and protocols, methods in molecular biology, vol 701. Springer, Berlin, pp 1–33
Birch RG (1997) Plant transformation: problems and strategies for practical application. Ann Rev Plant Mol Physiol 48:297–326
Boyko A, Blevins T, Yao Y, Golubov A, Bilichak A, Ilnytskyy Y, Hollunder J, Meins F Jr, Kovalchuk I (2010) Transgenerational adaptation of Arabidopsis to stress requires DNA methylation and the function of Dicer-like proteins. PLoS One 5: e9514. doi: 10.1371/journal.pone.0009514
Boyko A, Kovalchuk I (2011) Genome instability and epigenetic modification-heritable responses to environmental stress? Curr Opin Plant Biol 14:260–266
Butelli E, Titta L, Giorgio M, Mock HP, Matros A, Peterek S, Schijlen EGWM, Hall DR, Bovy AG, Luo J, Martin C (2008) Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors. Nat Biotech 26(11):1301–1308
Capell T, Christou P (2004) Progress in plant metabolic engineering. Curr Opin Biotechnol 15:148–154
Carlson SR, Rudgers GW, Zieler H, Mach J, Luo S, Grunden E, Krol C, Copenhaver O, Preuss D (2007) Meiotic transmission of an in vitro–assembled autonomous maize minichromosome. PLoS Genet 3(10):e179
Chen JH, Jiang HW, Hsieh EJ, Chen HY, Chien CT, Hsieh HL, Lin TP (2012) Drought and salt stress tolerance of an Arabidopsis glutathione S-transferase U17 knockout mutant are attributed to the combined effect of glutathione and abscisic acid. Plant Physiol 158:340–351
Chinnusamy V, Zhu JK (2009) Epigenetic regulation of stress responses in plants. Curr Opin Plant Biol 12:133–139
Chisti Y (2007) Biodiesel from microalgae. Biotechnol Adv 25:294–306
Chiu WL, Niwa Y, Zeng W, Hirano T, Kobayashi H, Sheen J (1996) Engineered GFP as a vital reporter in plants. Curr Biol 6:325–330
Chiu LW, Zhou X, Burke S, Wu X, Prior RL, Li L (2010) The purple cauliflower arises from activation of a MYB transcription factor. Plant Physiol 154:1470–1480
Collakova E, Jen JY, Senger RS (2012) Are we ready for genome-scale modeling in plants? Plant Sci 191:53–70
Copeland WB, Bartley BA, Chandran D, Galdzicki M, Kim KH, Sleight SC, Maranas CD, Sauru HM (2012) Computational tools for metabolic engineering. Metab Eng 14:270–280
Cramer C, Weissenborn DL, Oishi KK, Grabau EA, Bennett S, Ponce E, Grabowski GA, Radin D (1996) Bioproduction of human enzymes in transgenic tobacco. Ann N Y Acad Sci 792:62–71
Cubas P, Vincent C, Coen E (1999) An epigenetic mutation responsible for natural variation in floral symmetry. Nature 401:157–161
Cunningham FX Jr, Gantt E (2001) One ring or two? Determination of ring number in carotenoids by lycopene ε-cyclases. Proc Nat Acad Sci USA 98:2905–2910
Cunningham FX Jr, Chamovitz D, Misawa N, Gantt E, Hirschberg J (1993) Molecular cloning and expression in Escherichia coli of a cyanobacterial gene for lycopene cyclase, the enzyme that catalyzes the biosynthesis of β-carotene. FEBS Lett 328:130–138
De Cosa B, Moar W, Lee SB, Miller M, Daniell H (2001) Overexpression of the Bt cry2Aa2 operon in chloroplasts leads to formation of insecticidal crystals. Nat Biotechnol 19:71–74
De Groote ML, Verschure PJ, Rots MG (2012) Epigenetic Editing: targeted rewriting of epigenetic marks to modulate expression of selected target genes. Nucleic Acids Res 40:10596–10613
De Jaeger G, De Wilde C, Eeckhout D, Fiers E, Depicker A (2000) The plantibody approach: expression of antibody genes in plants to modulate plant metabolism or to obtain pathogen resistance. Plant Mol Biol 43:419–428
Decker EL, Reski R (2004) The moss bioreactor. Curr Opin Plant Biol 7:166–170
Decker EL, Reski R (2007) Moss bioreactors producing improved biopharmaceuticals. Curr Opin Biotech 18:393–398
DellaPenna D (2001) Plant metabolic engineering. Plant Physiol 125:160–163
Dixon RA (2005) Engineering of plant natural product pathways. Curr Opin Plant Biol 8:329–336
Farré G, Bai C, Twyman RM, Capell T, Christou P, Zhu C (2011) Nutritious crops producing multiple carotenoids–a metabolic balancing act. Trends Plant Sci 16:532–540
Feng S, Jacobsen SE (2011) Epigenetic modifications in plants: an evolutionary perspective. Curr Opin Plant Biol 14:179–186
Fire A, Xu S, Montgomery MK, Kostas SA, Driver SE, Mello CC (1998) Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 391:806–811
Floss DM, Schallau K, Rose-John S, Conrad U, Scheller J (2010) Elastin-like polypeptides revolutionize recombinant protein expression and their biomedical application. Trends Biotechnol 28:37–45
Forkmann G, Martens S (2001) Metabolic engineering and applications of flavonoids. Curr Opin Biotechnol 12:155–160
Gao J, Hooker BS, Anderson DB (2004) Expression of functional human coagulation factor XIII A-domain in plant cell suspensions and whole plants. Protein Exp Purif 37:89–96
Georgiev VG, Weber J, Kneschke EM, Denev PN, Bley T, Pavlov AI (2010) Antioxidant activity and phenolic content of betalain extracts from intact plants and hairy root cultures of the red beetroot Beta vulgaris cv. detroit dark red. Plant Foods Hum Nutr 65:105–111
Giuliano G, Bartley GE, Scolnik PA (1993) Regulation of carotenoid biosynthesis during tomato development. Plant Cell 5:379–387
Goldschmidt-Clermont M, Day A (2011) The chroplast transformation toolbox: selectable markers removal. Plant Biotechnol J 9:540–553
Goosens A, Häkkinen ST, Laakso I, Seppanen-Laakso T, Blondi S, De Sutter V, Lammertyn F et al (2003) A functional genomics approach toward understanding of secondary metabolism in plant cells. Proc Nat Acad Sci USA 100:8595–8600
Grabkowska R, Krolicka A, Mielicki W, Wielanek M, Wysokinska H (2010) Genetic transformation of Harpagophytum procumbens by Agrobacterium rhizogenes: iridoid and phenylethanoid glycoside accumulation in hairy root cultures. Acta Physiol Plant 32:665–673
Grotewold E (2008) Transcription factors for predictive plant metabolic engineering: are we there yet? Curr Opin Biotechnol 19:138–144
Grotewold E, Chamberlin M, Snook M, Siame B, Butler L, Swenson J, Maddock S, St Clair G, Bowen B (1998) Engineering secondary metabolism in maize cells bye ectopic expression of transcription factors. Plant Cell 10:721–740
Grusak MA, DellaPenna D (1999) Improving the nutrient composition of plants to enhance human nutrition and health. Ann Rev Plant Biol 50:133–161
Guda C, Lee SB, Daniell H (2000) Stable expression of a biodegradable protein-based polymer in tobacco chloroplasts. Plant Cell Rep 19:257–262
Hahn BS, Sim JS, Hyeong-Mi K, Mi-Young A, Hyo-Kyung P, Nan-A K, Yong-Hwan K (2009) Expression and characterization of human tissue-plasminogen activator in transgenic tobacco plants. Plant Mol Biol Rep 27:209–216
Halpin C (2005) Gene stacking in transgenic plants–the challenge for 21st century plant biotechnology. Plant Biotechnol J 3:141–155
Hamilton CM (1997) A binary BAC system for plant transformation with high-molecular-weight DNA. Gene 200:107–116
Hauser MT, Aufsatz W, Jonak C, Luschnig C (2011) Transgenerational epigenetic inheritance in plants. Biochem Biophys Acta (BBA)-Gene Regul Mech 1809:459–468
Hegeman AD (2010) Plant metabolomics-meeting the analytical challenges of comprehensive metabolite analysis. Brief Func Genomics 9:139–148
Hempel F, Lau J, Klingl A, Maier UG (2011) Algae as protein factories: expression of a human antibody and the respective antigen in the diatom Phaeodactylum tricornutum. PLoS ONE 6(12):e28424. doi:10.1371/journal.pone.0028424
Herbers K, Wilke I, Sonnewald U (1995) A thermostable xylanase from Clostridium thermocellum expressed at high levels in the apoplast of transgenic tobacco has no detrimental effects and is easily purified. Biotechnology 13:63–66
Herrera-Estrella L, De Block M, Messens EHJP, Hernalsteens JP, Van Montagu M, Schell J (1983) Chimeric genes as dominant selectable markers in plant cells. EMBO J 2:987
Hirsch CN, Robin-Buell C (2013) Tapping the promise of genomics in species with complex. Nonmodel Genomes Ann Rev Plant Biol 64:89–110
Isman MB, Miresmailli S, Machial C (2011) Commercial opportunities for pesticides based on plant essential oils in agriculture, industry and consumer products. Phytochem Rev 10:197–204
Israeli Y, Ben-Bassat D, Reuveni O (1995) In vitro culture of bananas. In: Gowen S (ed) Bananas and plantains. Chapman and Hall, London, pp 147–178
Jefferson RA, Kavanagh TA, Bevan MW (1987) GUS fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6:3901–3907
Johannes F, Porcher E, Teixeira FK, Saliba-Colombani V, Simon M, Agier N, Colot V (2009) Assessing the impact of transgenerational epigenetic variation on complex traits. PLoS Gen 5:e1000530
Joung JY, Kasthuri GM, Park JY, Kang WJ, Kim HS, Yoon BS, Joung H, Jeon JH (2003) An overexpression of chalcone reductase of Pueraria montana var. lobata alters biosynthesis of anthocyanin and 5'-deoxyflavonoids in transgenic tobacco. Biochem Biophys Res Commun 303:326–331
Jullien PE, Mosquna A, Ingouff M, Sakata T, Ohad N, Berger F (2008) Retinoblastoma and its binding partner MSI1 control imprinting in Arabidopsis. PLoS Biol 6:e194
Kakutani T, Munakata K, Richards EJ, Hirochika H (1999) Meiotically and mitotically stable inheritance of DNA hypomethylation induced by ddm1 mutation of Arabidopsis thaliana. Genetics 151:831–838
Karp A (1994) Origins, causes and uses of variation in plant tissue culture. In: Vassil IK, Thorpe TA (eds) Plant cell and tissue culture. Kluwer Academic Publishers, Dordrecht, pp 139–152
Karp A (1995) Somaclonal variation as a tool for crop improvement. Euphytica 85:295–302
Kawauchi M, Arima T, Shirota O, Sekita S, Nakane T, Takase Y, Kuroyanagi M (2010) Production of sesquiterpene-type phytoalexins by hairy roots of Hyoscyamus albus co-treated with copper sulfate and methyl Jasmonate. Chem Pharm Bull 58:934–938
Koya V, Moayeri M, Leppla SH, Daniell H (2005) Plant based vaccine: mice immunized with chloroplast-derived anthrax protective antigen survive anthrax lethal toxin challenge. Infect Immun 73:8266–8274
Kueger S, Steinhauser D, Willmatzer L, Giavalisco P (2012) High-resolution plant metabolomics: from mass spectral features to metabolites and from whole-cell analysis to subcellular metabolite distributions. Plant J 70:39–50
Larkin PJ (1998) Introduction. In: Jain SM, Brar DS, Ahloowalia BS (eds) Somaclonal variation and induced mutations in crop improvement. Kluwer Academic Publishers, Dordrecht, pp 3–13
Larkin P, Scowcroft W (1981) Somaclonal variation—a novel source of variability from cell cultures for plant improvement. Theor Appl Genet 60:197–214
Leite A, Kemper EL, da Silva MJ, Luchessi AD, Siloto RMP, Bonaccorsi ED, El-Dorry HF, Arruda P (2000) Expression of correctly processed human growth hormone in seeds of transgenic tobacco plants. Mol Breed 6:47–53
Li JWH, Vederas JC (2009) Drug discovery and natural products: end of an era or an endless frontier? Science 325:161–165
Lim EK, Bowles D (2012) Plant production systems for bioactive small molecules. Curr Opin Biotechnol 23:271–277
Liu YG, Shirano Y, Fukaki H, Yanai Y, Tasaka M, Tabata S, Shibata D (1999) Complementation of plant mutants with large genomic DNA fragments by a transformation-competent artificial chromosome vector accelerates positional cloning. Proc Nat Acad Sci USA 96:6535–6540
López-Arredondo DL, Herrera-Estrella L (2012) Engineering phosphorus metabolism in plants to produce a dual fertilization and weed control system. Nat Biotechnol 30:889–893
Lu S, Van Eck J, Zhou X, Lopez A, O’Halloran D, Cosman B, Conlin D, Paolillo B, Garvin D, Vrebalov J, Kochian V, Kupper H, Earle E, Cao J, Lia L (2006) The cauliflower Or gene encodes a DnaJ cysteine-rich domain containing protein that mediates high levels of β-carotene accumulation. Plant Cell 18:3594–3605
Ma JK, Hiatt A, Hein M, Vine ND, Wang F, Stabila P, van Dolleweerd C, Mostov K, Lehner T (1995) Generation and assembly of secretory antibodies in plants. Science 268:716–719
Ma JK, Drake PM, Chargelegue D, Obregon P, Prada A (2005) Antibody processing and engineering in plants, and new strategies for vaccine production. Vaccine 23:1814–1818
Maia MF, Moore SJ (2011) Plant-based insect repellents: a review of their efficacy, development and testing. Malaria J 10:S11. doi:10.1186/1475-2875-10-S1-S11
Martin C, Butelli E, Petroni K, Tonelli Ch (2011) How can research on plants contribute to promoting human health? Plant Cell 23:1685–1699
Mathur A, Gangwar A, Mathur AK, Verma P, Uniyal GC, Lal RK (2010) Growth kinetics and ginsenosides production in transformed hairy roots of American ginseng- Panax quinquefolium L. Biotechnol Lett 32:457–461
Mayfield SP, Franklin SE (2005) Expression of human antibodies in eukaryotic micro-algae. Vaccine 23:1828–1832
McCormick AA, Kumagai MH, Hanley K, Turpen TH, Hakim I, Grill LK, Tuse D, Levy A, Levy R (1999) Rapid production of specific vaccines for lymphoma by expression of the tumor-derived single-chain Fv epitopes in tobacco plants. Proc Nat Acad Sci USA 96:703–708
Menke FL, Champion A, Kijne JW, Memelink J (1999) A novel jasmonate-and elicitor-responsive element in the periwinkle secondary metabolite biosynthetic gene Str interacts with a jasmonate- and elicitor-inducible AP2-domain transcription factor, ORCA2. EMBO J 18:4455–4463
Miralpeix B, Rischer H, Häkkinen ST, Ritala A, Seppänen-Laakso T, Oksman-Caldentey KM, Capell T, Christou P (2013) Metabolic engineering of plant secondary metabolites: wich way the forward? Curr Pharm Des 19:5622–5639
Mitsuda N, Hiratsu K, Todaka D, Nakashima K, Yamaguchi-Shinozaki K, Ohme-Takagi M (2006) Efficient production of male and female sterile plants by expression of a chimeric repressor in Arabidopsis and rice. Plant Biotechnol J 4:325–332
Molina A, Hervaas-Stubbs S, Daniell H, Mingo-Castel AM, Veramendi J (2004) High-yield expression of a viral peptide animal vaccine in transgenic tobacco chloroplasts. Plant Biotechnol J 2:141–153
Moon-Yoon J, Zhao LY, Shanks JV (2013) Metabolic engineering with plants for a sustainable biobased economy. Ann Rev Chem Biomol Eng 4:211–237
Nandi S, Suzuki YA, Huang J, Yalda D, Pham P, Liying W, Bartley G, Ning H, Lonnerdal B (2002) Expression of human lactoferrin in transgenic rice grains for the application in infant formula. Plant Sci 163:713–722
Napoli C, Lemieux C, Jorgensen R (1990) Introduction of a chimeric chalcone synthase gene into petunia results in reversible co-suppression of homologous genes in trans. Plant Cell 2:279–289
Naqvi S, Zhu C, Farre G, Ramessar K, Bassie L, Breitenbach J, Conesa DP, Ros G, Sandmann G, Capell T et al (2009) Transgenic multivitamin corn through biofortification of endosperm with three vitamins representing three distinct metabolic pathways. Proc Nat Acad Sci USA 106:7762–7767
Naqvi S, Farré G, Sanahuja G, Capell T, Zhu C, Christou P (2010) When more is better? Trends Plant Sci 15:48–56
Nesi N, Debeaujon I, Jond C, Pelletier G, Caboche M, Lepiniec L (2000) The TT8 gene encodes a basic hélix-loop-helix domain protein required for expression of DFR and BAN genes in Arabidopsis siliques. Plant Cell 12:1863–1878
Nesi N, Jond C, Debeaujon I, Caboche M, Lepiniec L (2001) The Arabidopsis TT2 gene encodes an R2R3 MYB domain protein that acts as a key determinant for proanthocyanidin accumulation in developing seed. Plant Cell 13:2099–2114
Nie ZP, Zhao GP, Chen B, Zhang M, Ye Z, Hu L (2013) Brassica napus possesses enhanced antioxidant capacity via heterologous expression of anthocyanin pathway gene transcription factors. Russ J Plant Physiol 60:108–115
Nykiforuk CL, Boothe JG, Murray EW, Keon RG, Goron HJ, Markley NA, Moloney MM (2006) Transgenic expression and recovery of biologically active recombinant human insulin from Arabidopsis thaliana seeds. Plant Biotechnol J 4:77–85
Oksman-Caldentey KM, Inzé D (2004) Plant cell factories in the post-genomic era: new ways to produce designer secondary metabolites. Trends Plant Sci 9:433–440
Paine JA, Shipton CA, Chaggar S, Howells RM, Kennedy MJ, Vernon G, Drake R (2005) Improving the nutritional value of Golden Rice through increased pro-vitamin A content. Nat Biotechnol 23:482–487
Parmenter DL, Boothe JG, Peel GJ, Pang Y, Modolo LV, Dixon RA (2009) The LAP1 MYB transcription factor orchestrates anthocyanidin biosynthesis and glycosylation in Medicago. Plant J 59:136–149
Paszkowski J, Grossniklaus U (2011) Selected aspects of transgenerational epigenetic inheritance and resetting in plants. Curr Opin Plant Biol 14:195–203
Petit P, Grainer T, Langloisd′Estaintat B, Manigand C, Bathany K, Schimitter JM, Lauvergeat V, Hamdi S, Gallois B (2007) Crystal structure of grape dihydroflavonol-4-reductase, a key enzyme in flavonoid biosynthesis. J Mol Biol 368:1345–1357
Peyvandi M, Noormohammadi Z, Banihashemi O, Farahani F, Majd A, Hosseini-Mazinani M, Shedai M (2009) Molecular analisys of genetic stability in long term micropropagated shoots of Olea europea L. (cv. Dezful). Assian J Plant Sci 8:146–152
Pham NB, Schäfer H, Wink M (2012) Production and secretion of recombinant thaumatin in tobacco hairy root cultures. Biotechnol J. doi:10.1002/biot.201100430
Pickens LB, Tang Y, Chooi YH (2011) Metabolic engineering for the production of natural products. Ann Rev Chem Biomol 2:211–236
Pierantoni L, Dondini L, De Franceschi P, Musacchi S, Winkel-Shirley BJ, Sansavini S (2010) Mapping of an anthocyanin-regulating MYB transcription factor and its expression in red and green pear Pyrus communis. Plant Physiol Biochem 48(12):1020–1026
Plant Metab Net (2013) PMN database content statistics: current PMN 8.0 release July 2013. Stanford: plant metab net http://www.plantcyc.org/release_notes/content_statistics.faces#aracyc
Pollier J, Goossens A (2013) Metabolite profiling of plant tissues by liquid chromatography Fourier transform ion cyclotron resonance mass spectrometry. In: Jasmonate Signaling: Methods and protocols. Methods in Molecular Biology, vol 1011. Springer Bussines Media, New York, pp 277–286
Potvin G, Zhang Z (2010) Strategies for high-level recombinant protein expression in transgenic microalgae: a review. Biotechnol Adv 28:910–918
Prakash I, DuBois GE, Clos JF, Wilkens KL, Fosdick LE (2008) Development of rebiana, a natural, non-caloric sweetener. Food Chem Toxicol 46:S75–S82
Qaim M (2010) Benefits of genetically modified crops for the poor: household income, nutrition, and health. New Biotechnol 27:552–557
Qi B, Fraser T, Mugford S, Dobson G, Sayanova O, Butler J, Napier J, Stobar A, Lazarus CM (2004) Production of very long chain polyunsaturated omega-3 and omega-6 fatty acids in plants. Nat Biotechnol 22:739–745
Raja R, Hemaiswarya S, Kumar NA, Sridhar S, Rengasamy R (2008) A perspective on the biotechnological potential of microalgae. Crit Rev Microbiol 34:77–88
Ramachandra-Rao S, Ravishankar GA (2002) Plant cell cultures: chemical factories of secondary metabolites. Biotechnol Adv 10:101–153
Riechmann JL, Heard J, Martin G, Reuber L, Keddie J, Adam L, Pineda O, Ratcliffe OJ, Samaha R, Creelman R, Pilgrim M, Broun P, Zhang J, Ghandehari D, Sherman BK, Yu GL (2000) Arabidopsis transcription factors: genome-wide comparative analysis among eukaryotes. Science 290:2105–2110
Ruban AV, Young AJ, Pascal AA, Horton P (1994) The effects of illumination on the xanthophyll composition of the photosystem II light-harvesting complexes of spinach thylakoid membranes. Plant Physiol 104:227–234
Runguphan W, Maresh JJ, O’Connor SE (2009) Silencing of tryptamine biosynthesis for production of non-natural alkaloids in plant culture. Proc Nat Acad Sci USA 106:13673–13678
Saze H, Scheid OM, Paszkowski J (2003) Maintenance of CpG methylation is essential for epigenetic inheritance during plant gametogenesis. Nat Gen 34:65–69
Schijlen EGWM, Ric de vos CH, Van Tunen AJ, Bovy AG (2004) Modification of flavonoids biosynthesis in crop plants. Phytochemistry 65:2632–2648
Schwab W, Davidovich-Rikanati R, Lewinsohn E (2008) Biosynthesis of plant-derived flavor compounds. Plant J 54:712–732
Schwender J (2008) Metabolic flux analysis as a tool in metabolic engineering of plants. Curr Opin Biotechnol 19:131–137
Schwinn K, Venail J, Shang Y, Mackay S, Alm V, Butelli E, Oyama R, Bailey P, Davies K, Martin C (2006) A small family of MYB-regulatory genes controls floral pigmentation intensity and patterning in the genus Anthirrhinum. Plant Cell 18:831–851
Sethuraman N, Stadheim TA (2006) Challenges in therapeutic glycoprotein production. Curr Opin Biotechnol 17:341–346
Shadwick FS, Doran PM (2007) Infection, propagation, distribution and stability of plant virus in hairy root cultures. J Biotechnol 131:318–329
Shahijram L, Soneji J, Bollama K (2003) Analyzing somaclonal variation in micropropagated bananas (Musa spp.). In Vitro Cell Dev Biol Plant 39:551–556
Sharma AK, Sharma MK (2009) Plants as bioreactors: recent developments and emerging opportunities. Biotechnol Adv 27:811–832
Sijmons PC, Dekker BMM, Schrammeijer B, Verwoerd TC, van den Elzen PJM, Hoekema A (1990) Production of correctly processed human serum albumin in transgenic plants. Nat Biotechnol 8:217–221
Skarjinskaia M, Ruby K, Araujo A, Taylor K, Gopalasamy-Raju V, Musiychuk K, Chichester JA, Palmer GA, de la Rosa P, Mett V, Ugulava N, Streatfield SJ, Yusibov V (2013) Hairy roots as a vaccine production and delivery system. Adv Biochem Eng Biotechnol 134:115–134
Sone T, Nagamori E, Ikeuchi T, Mizukami A, Takakura Y, Kajiyama SI, Fukui K (2002) A novel gene delivery system in plants with calcium alginate micro-beads. J Biosci Bioeng 94:87–91
Stein H, Wilensky M, Tsafrir Y, Rosenthal M, Amir R, Avraham T, Ofir K, Dgany O, Yanon A, Shoseyov O (2009) Production of bioactive, post-translationally modified, heterotrimeric, human recombinant type-I collagen in transgenic tobacco. Biomacromolecules 10:2640–2645
Syklowska-Baranek K, Pietrosiuk A, Kokoszka A, Furmanowa M (2009) Enhancement of taxane production in hairy root culture of Taxus x media var Hicksii. J Plant Physiol 166:1950–1954
Tang G, Galili G, Zhuang X (2007) RNAi and microRNA: breakthrough technologies for the improvement of plant nutritional value and metabolic engineering. Metabolomics 3:357–369
Tissot G, Canard H, Nadai M, Martone A, Botterman J, Dubald M (2008) Translocation of aprotinin, a therapeutic protease inhibitor, into the thylakoid lumen of genetically engineered tobacco chloroplasts. Plant Biotechnol J 6:309–320
Tran M, Zhou B, Pettersson PL, Gonzalez MJ, Mayfield SP (2009) Synthesis and assembly of a full-length human monoclonal antibody in algal chloroplasts. Biotechnol Bioeng 104:663–673
Turpen TH, Reinl SJ, Charoenvit Y, Hoffman SL, Fallarme V, Grill LK (1995) Malaria epitopes expressed on the surface of recombinant tobacco mosaic virus. Nat Biotechnol 13:53–57
Twyman RM, Christou P, Stoger E (2002) Genetic transformation of plants and their cells. Plant Biotechnol and Transgenic Plants. Marcel Dekker Inc, New York, pp 111–141
Valderrama F, Arango I, Afanador K (2005) Plant transformation mediated by Agrobacterium: applied natural genetic engineering. Rev Fac Nal Agr Medellín 59:2569–2585
Van Erp H, Bates PD, Burgal J, Shockey J, Browse J (2011) Castor phospholipid: diacylglycerol acyltransferase facilitates efficient metabolism of hydroxy fatty acids in transgenic Arabidopsis. Plant Physiol 155:683–693
Vasil IK (1990) The realities and challenges of plant biotechnology. Bio/Technology 8:231–296
Verpoorte R, Memelink J (2002) Engineering secondary metabolite production in plants. Curr Opin Biotechnol 13:181–187
Wada N, Kajiyama SI, Akiyama Y, Kawakami S, No D, Uchiyama S, Otani M, Shimada T, Nose N, Suzuki G, Mukai Y, Fukui K (2009) Bioactive beads-mediated transformation of rice with large DNA fragments containing Aegilops tauschii genes. Plant Cell Rep 28:759–768
Walker TL, Purton S, Becker DK, Collet C (2005) Microalgae as bioreactors. Plant Cell Rep 24:629–641
Welle R, Grisbach J (1988) Isolation of anobel NADPH-dependent reductase wihich co-acts with chalcone synthase in the biosynthesis of 6’-deoxychalcone. FEBS Left 236:221–225
Wiechert W (2001) 13C metabolic flux analysis. Metab Eng 3:195–206
Wijffels RH, Barbosa MJ (2010) An outlook on microalgal biofuels. Science 329:796–799
Woolston BM, Edgar S, Stephanopoulos G (2013) Metabolic engineering: past and future. Ann Rev Chem Biomol Eng 4:259–288
Wu G, Truksa M, Datla N, Vrinten P, Bauer J, Zank T, Cirpus P, Heinz E, Qiu X (2005) Stepwise engineering to produce high yields of very long-chain polyunsaturated fatty acids in plants. Nat Biotechnol 23:1013–1017
Ye X, Al-Babili S, Klöti A, Zhang J, Lucca P, Beyer P, Potrykus I (2000) Engineering the provitamin A (β-carotene) biosynthetic pathway into (carotenoid-free) rice endosperm. Science 287:303–305
Yokotani N, Ichikawa T, Kondou Y, Iwabuchi M, Matsui M, Hirochika H, Oda K (2013) Role of the rice transcription factor JAmyb in abiotic stress response. J Plant Res 126:131–139
Yonekura-Sakakibara K, Fukushima A, Saito K (2013) Transcriptome data modeling for targeted plant metabolic engineering. Curr Opin Biotech 24:285–290
Yu W, Han F, Gao Z, Vega JM, Birchler JA (2007) Construction and behavior of engineered minichromosomes in maize. Proc Nat Acad Sci USA 104:8924–8929
Yu A, Lepère G, Jay F, Wang J, Bapaume L, Wang Y, Navarro L (2013) Dynamics and biological relevance of DNA demethylation in Arabidopsis antibacterial defense. Proc Nat Acad Sci USA 110:2389–2394
Zhang G, Chen M, Li L, Xu Z, Chen X, Guo J, Ma Y (2009) Overexpression of the soybean GmERF3 gene, an AP2/ERF type transcription factor for increased tolerances to salt, drought, and diseases in transgenic tobacco. J Exp Bot 60:3781–3796
Zhang Y, Yan YP, Wang ZZ (2010) The Arabidopsis PAP1transcription factor plays an important role in the enrichment of phenolic acids in Salvia miltiorrhiza. J Agric Food Chem 58:12168–12175
Zhang L, Wang Y, Zhang X, Zhang M, Han D, Qiu C, Ha Z (2012) Dynamics of phytohormone and DNA methylation patterns changes during dormancy induction in strawberry (Fragaria × ananassa Duch.). Plant Cell Rep 31:155–165
Zhu Z, Hughes KW, Huang L, Sun B, Liu C, Yuing L (1994) Expression of human alpha-interferon cDNA in transgenic rice plants. Plant Cell Tissue Organ Cult 36:197–204
Zuk M, Kulma A, Dymińska L, Szołtysek K, Prescha A, Hanuza J, Szopa J (2012) Flavonoid engineering of flax potentiate its biotechnological application. BMC Biotechnol 12(1):47
Zuluaga A, Gonzalia S, Loreti B, Pucciariello A, Degl’Innocenti C, Guidi C, Alpi D, Perata A (2007) Arabidopsis thaliana MYB75/PAP1 transcription factor induces anthocyanin production in transgenic tomato plants. Funct Plant Biol 35:606–618
Acknowledgments
We recognize financial support for projects related to this review by Consejo Nacional de Ciencia y Tecnología (CONACyT 134953) and Universidad Autónoma de Querétaro (FOFI-UAQ).
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Cruz-Ramírez, L.A. et al. (2014). Plants as Bioreactors for Human Health Nutrients. In: Guevara-Gonzalez, R., Torres-Pacheco, I. (eds) Biosystems Engineering: Biofactories for Food Production in the Century XXI. Springer, Cham. https://doi.org/10.1007/978-3-319-03880-3_15
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