Abstract
Cereals provide more than half the world population’s calorific intake, and have a variety of other important uses as food and beverage ingredients, livestock feeds, and as sources of renewable energy and industrial components. The technology to genetically modify many important cereals is now well-established, thereby presenting new opportunities to produce cereals with enhanced quality and novel properties. In 2007, GM (genetically modified) maize with insect and herbicide resistance was grown on over 30 million hectares worldwide, yet to date, there are no GM cereals with enhanced or novel grain (end-use) qualities being grown in commercial farmers’ fields. This review will discuss some of the latest GM technology developments reported to enhance the quality of cereals for food and other uses. Developments and opportunities involving gene manipulation for starch and protein quality, as well as non-starch polysaccharides, phenolic compounds and micronutrients will also be discussed. The current paucity of GM cereals with enhanced grain quality is not related to the absence of technological progress, rather it is the regulatory and consumer acceptance issues that have slowed the release of these crops.
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References
Able J. A.; Rathus C.; Godwin I. D. The investigation of optimal bombardment parameters for transient and stable transgene expression in sorghum. In Vitro Cell. Dev. Biol.-Plant 37: 341–348; 2001. doi:10.1007/s11627-001-0061-7.
Abrahams S.; Tanner G. J.; Larkin P. J.; Ashton A. R. Identification and biochemical characterisation of mutants in the proanthocyanidin pathway in Arabidopsis. Plant Physiol. 130: 561–576; 2002. doi:10.1104/pp.006189.
Albert S.; Delseny M.; Devic M. BANYULS, a novel negative regulator or flavonoid biosynthesis in the Arabidopsis seed coat. Plant J. 11: 289–299; 1997. doi:10.1046/j.1365-313X.1997.11020289.x.
Alloui-Lombarkia O.; Zemmouri F.; Smulikowska S.; Alloui N. In vitro effects of enzymes on the viscosity and non-starch polysaccharides of barley. Br. Poult. Sci. 44: 800–801; 2003. doi:10.1080/00071660410001666871.
Anderson O. Molecular approaches to cereal quality improvementIn: Henry R. J.; Kettlewell P. S. (eds) Cereal grain quality. Chapman & Hall, London, pp 371–404; 1996.
Appenzeller L.; Doblin M.; Barreiro R.; Wang H. Y.; Niu X. M.; Kollipara K.; Carrigan L.; Tomes D.; Chapman M.; Dhugga K. S. Cellulose synthesis in maize: isolation and expression analysis of the cellulose synthase (CesA) gene family. Cellulose 11: 287–299; 2004. doi:10.1023/B:CELL.0000046417.84715.27.
Austin S.; Bingham E. T.; Koegel R. G.; Mathews D. E.; Shahan M. N.; Straub R. J. An overview of a feasibility study for the production of industrial enzymes in transgenic alfalfa. In: Bajpai R. K.; Prokop A. (eds) Recombinant DNA technology II. New York Academy of Sciences, New York, pp 134–244; 1994.
Bai N.; Zhou Z.; Zhu N.; Zhang L.; Quan Z.; He K.; Zheng Q. Y.; Ho C. T. Antioxidative flavonoids from the flower of Inula britannica. J. Food Lipids 12: 141–149; 2005. doi:10.1111/j.1745-4522.2005.00012.x.
Bedford M. R.; Morgan A. J. The use of enzymes in poultry diets. Worlds Poult. Sci. J. 52: 61–68; 1996. doi:10.1079/WPS19960007.
Bellucci M.; Alpini A.; Arcioni S. Zein accumulation in forage species (Lotus corniculatus and Medicago sativa) and co-expression of the γ-zein:KDEL and β-zein:KDEL polypeptides in tobacco leaf. Plant Cell Rep. 20: 848–856; 2002. doi:10.1007/s00299-001-0413-0.
Bellucci M.; De Marchis F.; Mannucci R.; Bock R.; Arcioni S. Cytoplasm and chloroplasts are not suitable subcellular locations for β-zein accumulation in transgenic plants. J. Exp. Bot. 56: 1205–1212; 2005. doi:10.1093/jxb/eri114.
Beyer P.; Al-Babili S.; Ye X. D. Golden rice: Introducing the beta-carotene biosynthesis pathway into rice endosperm by genetic engineering to defeat vitamin A deficiency. J. Nutr. 132: 506S–510S; 2002.
Bird A. R.; Flory C.; Davies D. A.; Usher S.; Topping D. L. A novel barley cultivar (Himalaya 292) with specific gene mutation is starch synthase IIa raises large bowel starch and short chain fatty acid in rats. J. Nutr. 134: 831–835; 2004.
Buchanan B. B. Thioredoxin: a photosynthetic regulatory protein finds application in food improvement. J. Sci. Food Agric. 82: 45–52; 2002. doi:10.1002/jsfa.1002.
Buchanan B. B.; Adamidi C.; Lozano R. M.; Yee B. C.; Momma M.; Kobrehel K.; Ermel R.; Frick O. L. Thioredoxin-linked mitigation of allergic responses to wheat. Proc. Natl. Acad. Sci. USA 94: 5372–5377; 1997. doi:10.1073/pnas.94.10.5372.
Buchanan B. B.; Balmer Y. Redox regulation: a broadening horizon. Annu. Rev. Plant Biol. 56: 187–220; 2005. doi:10.1146/annurev.arplant.56.032604.144246.
Buchanan B. B.; Schürmann P.; Decottignies P.; Lozano R. M. Thioredoxin: a multifunctional regulatory protein with a bright future in technology and medicine. Arch. Biochem. Biophys. 314: 257–260; 1994. doi:10.1006/abbi.1994.1439.
Buckeridge M. S.; Rayon C.; Urbanowicz B.; Tine M. A. A.; Carpita N. C. Mixed linkage (1→3),(1→4)-β-d-glucans of grasses. Cereal Chem. 81: 115–127; 2004. doi:10.1094/CCHEM.2004.81.1.115.
Buffo R. A.; Weller C. L.; Gennadios A. Films from laboratory-extracted sorghum kafirin. Cereal Chem. 74: 473–475; 1997. doi:10.1094/CCHEM.1997.74.4.473.
Burn J. E.; Hocart C. H.; Birch R. J.; Cork A. C.; Williamson R. E. Functional analysis of the cellulose synthase genes CesA1, CesA2, and CesA3 in arabidopsis. Plant Physiol. 129: 797–807; 2002. doi:10.1104/pp.010931.
Burton R. A.; Gibeaut D. M.; Bacic A.; Findlay K.; Roberts K.; Hamilton A.; Baulcombe D. C.; Fincher G. B. Virus-induced silencing of a plant cellulose synthase gene. Plant Cell 12: 691–705; 2000.
Burton, R. A.; Jobling, S. A.; Harvey, A. J.; Shirley, N. J.; Mather, D. E.; Bacic, A.; Fincher, G. B. The genetics and transcriptional profiles of the cellulose synthase-like HvCslF gene family in barley (Hordeum vulgare L.). Plant Physiol. (in press); 2008. doi:10.1104/pp.107.114694; 2008.
Burton R. A.; Shirley N. J.; King B. J.; Harvey A. J.; Fincher G. B. The CesA gene family of barley. Quantitative expressionof transcripts reveals two groups of co-expressed genes. Plant Physiol. 134: 224–236; 2004. doi:10.1104/pp.103.032904.
Burton R. A.; Wilson S. M.; Hrmova M.; Harvey A. J.; Shirley N. J.; Medhurst A.; Stone B. A.; Newbigin E. J.; Bacic A.; Fincher G. B. Cellulose synthase-like CslF genes mediate the synthesis of cell wall (1,3;1,4)-β-d-glucans. Science 311: 1940–1942; 2006. doi:10.1126/science.1122975.
Byaruhanga Y. B.; Erasmus C.; Taylor J. R. N. Effect of microwave heating of kafirin on the functional properties of kafirin films. Cereal Chem. 82: 565–573; 2005. doi:10.1094/CC-82-0565.
Cheng M.; Fry J. E.; Pang S.; Zhou H.; Hironaka C. M.; Duncan D. R.; Conner T. W.; Wan Y. Genetic transformation of wheat mediated by Agrobacterium tumefaciens. Plant Physiol. 115: 971–980; 1997.
Chiang C. M.; Yeh F. S.; Huang L. F.; Tseng T. H.; Chung M. C.; Wang C. S.; Lur H. S.; Shaw J. F.; Yu S. M. Expression of a bi-functional and thermostable amylopullulanase in transgenic rice seeds leads to autohydrolysis and altered composition of starch. Mol. Breed. 15: 125–143; 2005. doi:10.1007/s11032-004-3919-7.
Cho M. -J.; Wong J. H.; Marx C.; Jiang W.; Lemaux P. G.; Buchanan B. B. Overexpression of thioredoxin h leads to enhanced activity of starch debranching enzyme (pullulanase) in barley grain. Proc. Natl. Acad. Sci. USA 96: 14641–14646; 1999. doi:10.1073/pnas.96.25.14641.
Ciceri P.; Castelli S.; Lauria M.; Lazzari B.; Genga A.; Bernard L.; Sturaro M.; Viotti A. Specific combinations of zein genes and genetic backgrounds influence the transcription of the heavy-chain zein genes in maize opaque-2 endosperms. Plant Physiol. 124: 451–460; 2000. doi:10.1104/pp.124.1.451.
Cone K. C.; Burr F. A.; Burr B. Molecular analysis of the maize anthocyanin regulatory locus C1. Proc.Natl. Acad. Sci. USA 83: 9631–9635; 1986. doi:10.1073/pnas.83.24.9631.
Consonni G.; Gavazzi G.; Dolfini S. Genetic analysis as a tool to investigate the molecular mechanisms underlying seed development in maize. Ann. Bot. 96: 353–362; 2005. doi:10.1093/aob/mci187.
Cook J. D.; Skikne B. S.; Baynes R. D. Iron deficiency: the global perspective. Adv. Exp. Med. Biol. 356: 219–228; 1994.
Crispeels M. J.; Sadava D. E. Plants, Genes and Crop Biotechnology. Jones and Bartlett, Sudbury, Mass, USA; 2003.
Cuq B.; Gontard N.; Guilbert S. Proteins as agricultural polymers for packaging production. Cereal Chem. 75: 1–9; 1998. doi:10.1094/CCHEM.1998.75.1.1.
Curtis, I. S. (ed) Transgenic crops of the world: essential protocols. Kluwer, Dordrecht, Netherlands; 2004.
Damerval C.; Le Guilloux M. Characterization of novel proteins affected by the o2 mutation and expressed during maize endosperm development. Mol. Gen. Genet. 257: 354–361; 1998. doi:10.1007/s004380050657.
da Silva L. S.; Taylor J. R. N. Sorghum bran as a potential source of kafirin. Cereal Chem. 81: 322–327; 2004. doi:10.1094/CCHEM.2004.81.3.322.
da Silva L. S.; Taylor J. R. N. Physical, mechanical, and barrier properties of kafirin films from red and white sorghum milling fractions. Cereal Chem. 82: 9–14; 2005. doi:10.1094/CC-82-0009.
Delmer D. P. Agriculture in the developing world: connecting innovations in plant research to downstream applications. Proc. Natl. Acad. Sci. USA 102: 15739–15746; 2005. doi:10.1073/pnas.0505895102.
Dias A.; Grotewold E. Manipulating the accumulation of phenolics in maize cultured cells using transcription factors. Biochem. Eng. J. 14: 207–216; 2003. doi:10.1016/S1369-703X(02)00225-5.
Dixon R. A.; Xie D.; Sharma S. B. Proanthocyanidins—a final frontier in flavonoid research? New Phytol. 165: 9–28; 2005. doi:10.1111/j.1469-8137.2004.01217.x.
Duan M.; Sun S. S. M. Profiling the expression of genes controlling rice grain quality. Plant Mol. Biol. 59: 165–178; 2005. doi:10.1007/s11103-004-7507-3.
Duodu K. G.; Nunes A.; Delgadillo I.; Parker M. L.; Mills E. N. C.; Belton P. S.; Taylor J. R. N. Effect of grain structure and cooking on sorghum and maize in vitro protein digestibility. J. Cereal Sci. 35: 161–174; 2002. doi:10.1006/jcrs.2001.0411.
Duodu K. G.; Taylor J. R. N.; Belton P. S.; Hamaker B. R. Factors affecting sorghum protein digestibility. J. Cereal Sci. 38: 117–131; 2003. doi:10.1016/S0733-5210(03)00016-X.
Edwards A.; Marshall J.; Sidebottom C.; Visser R. G. F.; Smith A. M.; Martin C. Biochemical and molecular characterisation of a novel starch synthase from potato tubers. Plant J. 8: 283–294; 1995. doi:10.1046/j.1365-313X.1995.08020283.x.
Emmambux N. M.; Taylor J. R. N. Sorghum kafirin interaction with various phenolic compounds. J. Sci. Food Agric. 83: 402–407; 2003.
Evers A. D.; Blakeney A. B.; O’Brien L. O. Cereal structure and composition. Aus. J. Agric. Res. 50: 629–650; 1999. doi:10.1071/AR98158.
Ezeogu L. I.; Duodu K. G.; Taylor J. R. N. Effects of endosperm texture and cooking conditions on the in vitro starch digestibility of sorghum and maize flours. J. Cereal Sci. 42: 33–44; 2005. doi:10.1016/j.jcs.2005.02.002.
Falco S. C.; Guida T.; Locke M.; Mauvais J.; Sanders C.; Ward R. T.; Webber P. Transgenic canola and soybean seeds with increased lysine. Nat. Biotechnol. 13: 577–582; 1995. doi:10.1038/nbt0695-577.
FAO. FAO Statistical Databases: http://faostat.fao.org; 2004.
Ferreira R. R.; Varisi V. A.; Meinhardt L. W.; Lea P. J.; Azevedo R. A. Are high-lysine cereal crops still a challenge? Braz. J. Med. Biol. Res. 38: 985–994; 2005.
Fincher G. B.; Stone B. A. Cell walls their components in cereal grain technology. Adv. Cereal Sci. Technol. 8: 207–295; 1986.
Fornazier R. F.; Gaziola S. A.; Helm C. V.; Lea P. J.; Azevedo R. A. Isolation and characterization of enzymes involved in lysine catabolism from sorghum seeds. J. Agric. Food Chem. 53: 1791–1798; 2005. doi:10.1021/jf048525o.
Frame B. R.; Shou H.; Chikwamba R. K.; Zhang Z.; Xiang C.; Fonger T. M.; Pegg S. E. K.; Li B.; Nettleton D. S.; Pei D.; Wang K. Agrobacterium tumefaciens-mediated transformation of maize embryos using a standard binary vector system. Plant Physiol. 129: 13–22; 2002. doi:10.1104/pp.000653.
Frame B. R.; Zhang H.; Coccioline S. M.; Siderenko L. V.; Dietrich C. R.; Pegg S. E.; Zhen S.; Schabel P. S.; Wang K. Production of transgenic maize from bombarded type II callus: effect of gold particle size and callus morphology on transformation efficiency. In Vitro Cell. Dev. Biol.-Plant 36: 21–29; 2000. doi:10.1007/s11627-000-0007-5.
Galili G. New insights into the regulation and functional significance of lysine metabolism in plants. Annu. Rev. Plant Biol. 53: 27–43; 2002. doi:10.1146/annurev.arplant.53.091401.110929.
Galili G.; Höfgen R. Metabolic engineering of amino acids and storage proteins in plants. Metab. Eng. 4: 3–11; 2002. doi:10.1006/mben.2001.0203.
Gao Z.; Xie X.; Ling Y.; Muthukrishnan S.; Liang G. Agrobacterium tumefaciens-mediated sorghum transformation using a mannose selection system. Plant Biotech. J. 3: 591–598; 2005. doi:10.1111/j.1467-7652.2005.00150.x.
Gelhaye E.; Rouhier N.; Jacquot J.-P. The thioredoxin h system of higher plants. Plant Physiol. Biochem. 42: 265–271; 2004. doi:10.1016/j.plaphy.2004.03.002.
Gennadios A.; Rhim J. W.; Handa A.; Weller C. L.; Hanna M. A. Ultraviolet radiation affects physical and molecular properties of soy protein films. J. Food Sci. 63: 225–228; 1998.
Gianibelli, M. C.; Larroque, O. R.; MacRitchie, F.; Wrigley, C. W. Biochemical, genetic, and molecular characterization of wheat endosperm proteins. Online Review, Cereal Chem. 2001.
Gibbon B. C.; Larkins B. A. Molecular genetic approaches to developing quality protein maize. Trends Genet. 21: 227–233; 2005. doi:10.1016/j.tig.2005.02.009.
Goff S. A.; Cone K. C.; Chandler V. L. Functional analysis of the transcriptional activator encoded by the maize B gene—evidence for a direct functional interaction between 2 classes of regulatory proteins. Genes Dev. 6: 864–875; 1992. doi:10.1101/gad.6.5.864.
Greenwall P.; Schofield J. D. A starch granule protein associated with endosperm softness in wheat. Cereal Chem. 63: 379–380; 1986.
Grotewold E.; Chamberlain M.; St. Claire G.; Swenson J.; Siame B. A.; Butler L. G.; Snook M.; Bowen B. Engineering secondary metabolism in maize cells by ectopic expression of transcription factors. Plant Cell 10: 721–740; 1998.
Hamaker, B. R.; Bugusu, B. A.; Sorghum proteins and food quality. In Belton, P. S.; Taylor, J. R. N. (eds) Afripro Conference Proceedings, www.afripro.org.uk. Paper 08; 2003.
Han X. Z.; Benmoussa M.; Gray J. A.; BeMiller J. N.; Hamaker B. R. Detection of proteins in starch granule channels. Cereal Chem. 82: 351–355; 2005. doi:10.1094/CC-82-0351.
Hiei Y.; Komari T.; Kumashiro T. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J. 6: 271–282; 1994. doi:10.1046/j.1365-313X.1994.6020271.x.
Hinchliffe D. J.; Kemp J. D. ß-Zein protein bodies sequester and protect the 18-kDa ß-zein protein from degradation. Plant Sci. 163: 741–752; 2002. doi:10.1016/S0168-9452(02)00177-2.
Hogberg A.; Lindberg J. E. Influence of cereal non-starch polysaccharides on digestion site and gut environment in growing pigs. Livest. Prod. Sci. 87: 121–130; 2004. doi:10.1016/j.livprodsci.2003.10.002.
Holland N.; Holland D.; Helentjaris T.; Dhugga K. S.; Xoconostle-Cazares B.; Delmer D. P. A comparative analysis of the plant cellulose synthase (CesA) gene family. Plant Physiol. 123: 1313–1323; 2000. doi:10.1104/pp.123.4.1313.
Holtekjolen A. K.; Uhlen A. K.; Brathen E.; Sahlstrom S.; Knutsen S. H. Content of starch and non-starch polysaccharides in barley varieties of different origin. Food Chem. 94: 348–358; 2006. doi:10.1016/j.foodchem.2004.11.022.
Hong C. W.; Cheng K. J.; Tseng T. H.; Wang C. S.; Liu L. F.; Yu S. M. Production of two highly active bacterial phytases with broad pH optima in germinated transgenic rice seeds. Transgenic Res. 13: 29–39; 2004. doi:10.1023/B:TRAG.0000017158.96765.67.
Hrmova M.; Fincher G. B. Structure–function relationships of beta-d-glucan endo- and exohydrolases from higher plants. Plant Mol. Biol. 47: 73–91; 2001. doi:10.1023/A:1010619128894.
Hu T.; Metz S.; Chay C.; Zhou H. P.; Biest N.; Chen G.; Cheng M.; Feng X.; Radionenko M.; Lu F.; Fry J. Agrobacterium-mediated large-scale transformation of wheat (Triticum aestivum L.) using glyphosate selection. Plant Cell Rep. 21: 1010–1019; 2003. doi:10.1007/s00299-003-0617-6.
Huang S.; Adams W. R.; Zhou Q.; Malloy K. P.; Voyles D. A.; Anthony J.; Kriz A. L.; Luethy M. H. Improving nutritional quality of maize proteins by expressing sense and antisense zein genes. J. Agric. Food Chem. 52: 1958–1964; 2004. doi:10.1021/jf0342223.
Huang S.; Kruger D. E.; Frizzi A.; D’Ordine R. L.; Florida C. A.; Adams W. R.; Brown W. E.; Luethy M. H. High-lysine corn produced by the combination of enhanced lysine biosynthesis and reduced zein accumulation. Plant Biotechnol. J. 3: 555–569; 2005. doi:10.1111/j.1467-7652.2005.00146.x.
Hunter B. G.; Beatty M. K.; Singletary G. W.; Hamaker B. R.; Dilkes B. P.; Larkins B. A.; Jung R. Maize opaque endosperm mutations create extensive changes in patterns of gene expression. Plant Cell 14: 2591–2612; 2002. doi:10.1105/tpc.003905.
Hurrell R. F.; Juillerat M. A.; Reddy M. B.; Lynch S. R.; Dassenko S. A.; Cook J. D. Soy protein, phytate and iron absorption in humans. Am. J. Clin. Nutr. 56: 573–578; 1992.
Hwang Y. S.; Ciceri P.; Parsons R. L.; Moose S. P.; Schmidt R. J.; Huang N. The maize O2 and PBF proteins act additively to promote transcription from storage protein gene promoters in rice endosperm cells. Plant Cell Physiol. 45: 1509–1518; 2004. doi:10.1093/pcp/pch173.
Izquierdo L.; Godwin I. D. Molecular characterization of a novel methionine-rich delta-kafirin seed storage protein gene in sorghum (Sorghum bicolor L.). Cereal Chem. 82: 706–710; 2005. doi:10.1094/CC-82-0706.
Jadhav S. J.; Lutz S. E.; Ghorpade V. M.; Salunkhe D. K. Barley: chemistry and value-added processing. Crit. Rev. Food Sci. Nutr. 38: 123–171; 1998. doi:10.1080/10408699891274183.
James, C. International Service for the Acquisition of Agri-Biotech Applications. http://www.isaaa.org/; 2008.
Jobling S. Improving starch for food and industrial applications. Curr. Opin. Plant Sci. 7: 210–218; 2004. doi:10.1016/j.pbi.2003.12.001.
Jones H. D. Wheat transformation: current technology and applications to grain development and composition. J. Cereal Sci. 41: 137–147; 2005. doi:10.1016/j.jcs.2004.08.009.
Jouany, J. P. Rumen microbial metabolism and ruminant digestion. Institut National de la Recherche Agronomique, Paris; 1991.
Joudrier P.; Gautier M. F.; de Lamotte F.; Kobrehel K. The thioredoxin h system: potential applications. Biotechnol. Adv. 23: 81–85; 2005. doi:10.1016/j.biotechadv.2004.09.003.
Kaliatzandonakes N. A farm-level perspective on agrobiotechnology: how much value for whom? AgBioForum 2: 61–64; 1999.
Kim C. S.; Woo Y.-M.; Clore A. M.; Burnett R. J.; Carneiro N. P.; Larkins B. A. Zein protein interactions, rather than the asymmetric distribution of zein mRNAs on endoplasmic reticulum membranes, influences protein body formation in maize endosperm. Plant Cell 14: 655–672; 2002. doi:10.1105/tpc.010431.
Koller A.; Washburn M. P.; Lange B. M.; Andon N. L.; Deciu C.; Haynes P. A.; Hays L.; Schieltz D.; Ulaszek R.; Wei J.; Woltes D.; Yates J. R. III Proteomic survey of metabolic pathways in rice. Proc. Natl. Acad. Sci. USA 99: 11969–11974; 2002. doi:10.1073/pnas.172183199.
Kumari S. R.; Chandrashekar A. Relationship between grain vitreousness and the contents of prolamins and three anti-fungal proteins in sorghum. J. Cereal Sci. 20: 93–99; 1994. doi:10.1006/jcrs.1994.1049.
Larkins B. A.; Vasil I. K. Cellular and molecular biology of plant seed development. Kluwer, The Netherlands; 1997.
Lechelt C.; Peterson T.; Laird A.; Chen J.; Dellaporta S. L.; Dennis E.; Peacock W. J.; Starlinger P. Isolation and molecular analysis of the maize P-locus. Mol. Gen. Genet. 219: 225–234; 1989. doi:10.1007/BF00261181.
Lee T. T. T.; Chung M.-C.; Kao Y.-W.; Wang C.-S.; Chen L.-J.; Tzen J. T. C. Specific expression of a sesame storage protein in transgenic rice bran. J. Cereal Sci. 41: 23–29; 2005. doi:10.1016/j.jcs.2004.08.014.
Lending C. R.; Larkins B. A. Changes in the zein composition of protein bodies during maize endosperm development. Plant Cell 1: 1011–1023; 1989.
Li Z.; Meyer S.; Essig J. S.; Liu Y.; Schapaugh M. A.; Muthukrishnan S.; Hainline B. E.; Trick H. N. High-level expression of maize γ-zein protein in transgenic soybean (Glycine max). Mol. Breed. 16: 11–20; 2005. doi:10.1007/s11032-004-7658-6.
Lin S.-K.; Chang M.-C.; Tsai Y.-G.; Lur H.-S. Proteomic analysis of the expression of proteins related to rice quality during caryopsis development and the effect of high temperature on expression. Proteomics 5: 2140–2156; 2005. doi:10.1002/pmic.200401105.
Lucca P.; Hurrell R.; Potrykus I. Genetic engineering approaches to improve the bioavailability and the level of iron in rice grains. Theor. Appl. Genet. 102: 392–397; 2001. doi:10.1007/s001220051659.
MacGregor A. W.; Fincher G. B. Carbohydrates of the barley grain. In: MacGregor A. W.; Bhatty R. S. (eds) Barley: chemistry and technology. AACC, St. Paul, MN, pp 73–130; 1993.
Macri L. J.; MacGregor A. W.; Schroeder S. W.; Bazin S. L. Detection of a limit dextrinase in inhibitor in barley. J. Cereal Sci. 18: 103–106; 1993. doi:10.1006/jcrs.1993.1038.
Marles M. A. S.; Ray H.; Gruber M. Y. New perspectives on proanthocyanin biochemistry and molecular regulation. Phytochemistry 64: 367–383; 2003. doi:10.1016/S0031-9422(03)00377-7.
Mazur B.; Krebbers E.; Tingey S. Gene discovery and product development for grain quality traits. Science 285: 372–375; 1999. doi:10.1126/science.285.5426.372.
Meng X.; Slominski B. A. Nutritive values of corn, soybean meal, canola meal, and peas for broiler chickens as affected by a multicarbohydrase preparation of cell wall degrading enzymes. Poult. Sci. 84: 1242–1251; 2005.
Meng F.; Wei Y.; Yang X. Iron content and bioavailability in rice. J. Trace Elem. Med. Biol. 18: 333–338; 2005. doi:10.1016/j.jtemb.2005.02.008.
Mertz E. T.; Bates L. S.; Nelson O. E. Mutant gene that changes the protein composition and increases the lysine content of maize endosperm. Science 145: 279–280; 1964. doi:10.1126/science.145.3629.279.
Morell M. K.; Kosar-Hashemi B.; Cmiel M.; Samuel M. S.; Chandler P.; Rahman S.; Buleon A.; Batey I. L.; Li Z. Barley sex6 mutants lack starch synthase IIa activity and contain a starch with novel properties. Plant J. 34: 173–185; 2003. doi:10.1046/j.1365-313X.2003.01712.x.
Morell M. K.; Myers A. M. Towards the rational design of cereal starches. Curr. Opin. Plant Biol. 8: 204–210; 2005. doi:10.1016/j.pbi.2005.01.009.
Morita T.; Kasaoka S.; Oh-hashi A.; Ikai M.; Numasaki Y.; Kiriyama S. Resistant proteins alter cecal short-chain fatty acid profiles in rats fed high amylose cornstarch. J. Nutr. 128: 1156–1164; 1998.
Morita T.; Kiriyama S. Mass production method for rice protein isolation and nutritional evaluation. J. Food Sci. 58: 1393–1397; 1993. doi:10.1111/j.1365-2621.1993.tb06190.x.
Nandi S.; Suzuki Y. A.; Huang J.; Yalda D.; Pham P.; Wu L.; Bartley G.; Huang N.; Lonnerdal B. Expression of human lactoferrin in transgenic rice grains for the application in infant formula. Plant Sci. 163: 713–722; 2002. doi:10.1016/S0168-9452(02)00165-6.
Onyango B. M.; Nayga R. M. Consumer acceptance of nutritionally enhanced genetically modified food: relevance of gene transfer technology. J. Agric. Resource Econ. 29: 567–583; 2004.
Oomen R. J. F. J.; Tzitzikas E. N.; Bakx E. J.; Straatman-Engelen I.; Bush M. S.; McCann M. C.; Schols H. A.; Visser R. G. F.; Vincken J.-P. Modulation of cellolose content of tuber cell walls by antisense expression of different potato (Solanum tuberosum L.) CesA clones. Phytochemistry 65: 535–546; 2004. doi:10.1016/j.phytochem.2003.12.019.
Oria M. P.; Hamaker B. R.; Shull J. M. Resistance of sorghum α-, β-, and γ-kafirins to pepsin digestion. J. Agric. Food Chem. 43: 2148–2153; 1995. doi:10.1021/jf00056a036.
Paine J. A.; Shipton C. A.; Chaggar S.; Howells R. M.; Kennedy M. J.; Vernon G.; Wright S. Y.; Hinchliffe E.; Adams J. L.; Silverstone A. L.; Drake R. A new version of Golden Rice with increased pro-vitamin A content. Nat. Biotechnol. 23: 482–487; 2005. doi:10.1038/nbt1082.
Pear J. R.; Kawagoe Y.; Schreckengost W. E.; Delmer D. P.; Stalker D. M. Higher plants contain homologs of the bacterial celA genes encoding the catalytic subunit of cellulose synthase. Proc. Natl. Acad. Sci. USA 93: 12637–12642; 1996. doi:10.1073/pnas.93.22.12637.
Pedersen J. F.; Bean S. R.; Graybosch R. A.; Park S. H.; Tilley M. Characterization of waxy grain sorghum lines in relation to granule-bound starch synthase. Euphytica 144: 151–156; 2005. doi:10.1007/s10681-005-5298-5.
Potrykus I. Golden rice and beyond. Plant Physiol. 125: 1157–1161; 2001. doi:10.1104/pp.125.3.1157.
Potrykus I. Nutritionally enhanced rice to combat malnutrition disorders of the poor. Nutr. Rev. 61part 6: 101–104; 2003doi:10.1301/nr.2003.jun.101-104.
Prins R. A.; Stewart C. S. Micro-organisms in ruminant nutrition. Nottingham University Press, Nottingham; 1994.
Rahman S.; Bird A.; Regina A.; Li Z.; Ral J. P.; McMaugh S.; Topping D.; Morell M. Resistant starch in cereals: Exploiting genetic engineering and genetic variation. J. Cereal Sci. 46: 251–260; 2007. doi:10.1016/j.jcs.2007.05.001.
Ray H.; Yu M.; Auser P.; Blahut-Beatty L.; McKersie B.; Bowley S.; Westcott N.; Coulman B.; Lloyd A.; Gruber M. Y. Expression of anthocyanin and proanthocyanidin following transformation of alfalfa with maize Lc. Plant Physiol. 132: 1–16; 2003. doi:10.1104/pp.103.025361.
Regina A.; Bird A.; Topping D.; Bowden S.; Freeman J.; Barsby T.; Kosar-Hashemi B.; Li Z.; Rahman S.; Morell M. High-amylose wheat generated by RNA interference improves indices of large-bowel health in rats. Proc. Natl. Acad. Sci. USA 103: 3546–3551; 2006. doi:10.1073/pnas.0510737103.
Riley, P.; Hoffman, L. Value-enhanced crops: biotechnology’s next stage. Agricultural Outlook. March:18–23; 1999.
Roy S.; Weller C. L.; Gennadios A.; Zeece M. G.; Testin R. F. Physical and molecular properties of wheat gluten films cast from heated film-forming solutions. J. Food Sci. 64: 57–60; 1999. doi:10.1111/j.1365-2621.1999.tb09860.x.
Sainz M. B.; Grotewold E.; Chandler V. L. Evidence for direct activation of an anthocyanin promoter by the maize C1 protein and comparison of DNA binding by related Myb domain proteins. Plant Cell 9: 611–625; 1997.
Saxena I. M.; Brown R. M. Cellulose biosynthesis: current views and evolving concepts. Ann. Bot. 96: 9–21; 2005. doi:10.1093/aob/mci155.
Schmidt R. J.; Burr F. A.; Burr B. Transposon tagging and molecular analysis of the maize regulatory locus opaque-2. Science 238: 960–963; 1987. doi:10.1126/science.2823388.
Schure M.; Wessler S.; Federoff N. Molecular identification and isolation of the waxy locus in maize. Cell 35: 225–233; 1983. doi:10.1016/0092-8674(83)90225-8.
Seetharaman K.; Tziotis A.; Borras F.; White P. J.; Ferrer M.; Robutti J. Thermal and functional characterization of corn from the Argentinean germplasm. Cereal Chem. 78: 379–386; 2001. doi:10.1094/CCHEM.2001.78.4.379.
Segal G.; Song R.; Messing J. A new opaque variant of maize by a single dominant RNA-interference-inducing transgene. Genetics 165: 387–397; 2003.
Sharma S. B.; Dixon R. A. Metabolic engineering of proanthocyanidins by ectopic expression of transcription factors in Arabidopsis thaliana. Plant J. 44: 62–75; 2005. doi:10.1111/j.1365-313X.2005.02510.x.
Sharma S. B.; Hancock K. R.; Ealing P. M.; White D. W. R. Expression of a sulfur-rich maize seed storage protein, γ-zein, in white clover (Trifolium repens) to improve forage quality. Mol. Breed. 4: 435–448; 1998. doi:10.1023/A:1009656002068.
Shaul O.; Galili G. Concerted regulation of lysine and threonine synthesis in tobacco plants expressing bacterial feedback-insensitive aspartate kinase and dihydrodipicolinate synthase. Plant Mol. Biol. 23: 759–768; 1993. doi:10.1007/BF00021531.
Shewry P. R.; Halford N. G. Cereal seed storage proteins: structures, properties and role in grain utilization. J. Exp. Bot. 53: 947–958; 2002. doi:10.1093/jexbot/53.370.947.
Shewry P. R.; Jones H. D. Transgenic wheat: where do we stand after the first 12 years? Ann. Appl. Biol. 147: 1–14; 2005. doi:10.1111/j.1744-7348.2005.00009.x.
Shewry P. R.; Tatham A. S. Disulphide bonds in wheat gluten proteins. J. Cereal Sci. 25: 207–227; 1997. doi:10.1006/jcrs.1996.0100.
Shewry P. R.; Tatham A. S.; Barro F.; Barcelo P.; Lazzeri P. Biotechnology of breadmaking—unravelling and manipulating the multi-protein gluten complex. Bio/Technology 13: 1185–1190; 1995. doi:10.1038/nbt1195-1185.
Shirley B. W. Flavonoids in seeds and grains: physiological function, agronomic importance and the genetics of biosynthesis. Seed Sci. Res. 8: 412–422; 1998.
Skylas D. J.; Van Dyk D.; Wrigley C. W. Proteomics of wheat grain. J. Cereal Sci. 41: 165–179; 2005. doi:10.1016/j.jcs.2004.08.010.
Smidansky E. D.; Clancy M.; Meyers F. D.; Lanning S. P.; Blake N. K.; Talbert L. E.; Giroux M. J. Enhance ADP-glucose pyrophosphorylase activity in wheat endosperm increases seed yield. Proc. Natl. Acad. Sci. USA 99: 1724–1729; 2002. doi:10.1073/pnas.022635299.
Smidansky E.; Martin J.; Hannah L.; Fischer A.; Giroux M. Seed yield and plant biomass increases in rice are conferred by deregulation of endosperm ADP-glucose pyrophosphorylase. Planta 216: 656–664; 2003.
Smith A. M. The biosynthesis of starch granules. Biomacromolecules 2: 335–341; 2001. doi:10.1021/bm000133c.
Song R.; Llaca V.; Linton E.; Messing J. Sequence, regulation, and evolution of the maize 22-kDa α zein gene family. Genome Res. 11: 1817–1825; 2001.
Song R.; Segal G.; Messing J. Expression of the sorghum 10-member kafirin gene cluster in maize endosperm. Nucleic Acids Res. 32: e189; 2004. doi:10.1093/nar/gnh183.
Spencer J. D.; Allee G. L.; Saubert T. E. Growth finishing performance and carcass characteristics of pigs fed normal and genetically modified low-phytate corn. J. Anim. Sci. 78: 1529–1536; 2000.
Stark D. M.; Timmerman K. P.; Barry G. F.; Priess J.; Kishore G. M. Regulation of the amount of starch in plant tissues by ADP glucose pyrophosphorylase. Science 258: 287–292; 1992. doi:10.1126/science.258.5080.287.
Streatfield S. J.; Lane J. R.; Brooks C. R.; Barker D. K.; Poage M. L.; Mayor J. M.; Lamphear B. J.; Drees C. F.; Jilka J. M.; Hood E. E.; Howard J. A. Corn as a production system for human and animal vaccines. Vaccine 21: 812–815; 2003. doi:10.1016/S0264-410X(02)00605-9.
Sun S. S. M.; Liu Q. Transgenic approaches to improve the nutritional quality of plant proteins. In Vitro Cell. Dev. Biol.-Plant 40: 155–162; 2004. doi:10.1079/IVP2003517.
Sweeten J. M. Livestock and poultry waste management: a national overview. In: Blake J.; Donald J.; Magette W. (eds) National livestock, poultry and aquaculture waste management. Amer. Soc. Agric. Eng., St Joseph, MI, pp 4–15; 1992.
Tanaka K.; Murata K.; Yamazaki M.; Onosato K.; Miyao A.; Hirochika H. Three distinct rice cellulose synthase catalytic subunit genes required for cellulose synthesis in the secondary wall. Plant Physiol. 133: 73–83; 2003. doi:10.1104/pp.103.022442.
Teli N. P.; Timko M. P. Recent developments in the use of transgenic plants for the production of human therapeutics and biopharmaceuticals. Plant Cell Tissue Organ Cult. 79: 125–145; 2004. doi:10.1007/s11240-004-0653-0.
Terada R.; Nakajima M.; Isshiki M.; Okagaki R. J.; Wessler S. R.; Shimamoto K. Antisense Waxy genes with highly active promoters effectively suppress Waxy gene expression in transgenic rice. Plant Cell Physiol. 41: 881–888; 2000. doi:10.1093/pcp/pcd008.
Tetlow I. J.; Morell M. K.; Emes M. J. Recent developments in understanding the regulation of starch metabolism in higher plants. J. Exp. Bot. 55: 2131–2145; 2004. doi:10.1093/jxb/erh248.
Topping D. Cereal complex carbohydrates and their contribution to human health. J. Cereal Sci. 46: 220–229; 2007. doi:10.1016/j.jcs.2007.06.004.
Topping D. L.; Clifton P. M. Short-chain fatty acids and human colonic function: roles of resistant starch and nonstarch polysaccharides. Physiol. Rev. 81: 1031–1064; 2001.
Topping D. L.; Gooden J. M.; Brown I. L.; Biebrick D. A.; McGrath L.; Trimble R. P.; Choct M.; Illman R. J. A high amylose (amylomaize) starch raises proximal large bowel starch and increases colon length in pigs. J. Nutr. 127: 615–622; 1997.
Vachon C.; D’Aprano G.; Lacroix M.; Letendre M. Effect of edible coating process and irradiation treatment of strawberry Fragaria spp. on storage-keeping quality. J. Food Sci. 68: 608–612; 2003. doi:10.1111/j.1365-2621.2003.tb05718.x.
Veum T. L.; Ledoux D. R.; Bollinger D. W. Low-phytic acid barley improves calcium and phosphorus utilization and growth performance in growing pigs. J. Anim. Sci. 80: 2663–2670; 2002.
Visser R. G. F.; Somhorst I.; Kuipers G. J.; Ruys N. J.; Feenstra W. J.; Jacobsen E. Inhibition of the expression of the gene for granule-bound starch synthase in potato by antisense constructs. Mol. Gen. Genet. 225: 289–296; 1991. doi:10.1007/BF00269861.
Vitale A.; Ceriotti A. Protein quality control mechanisms and protein storage in the endoplasmic reticulum. A conflict of interests? Plant Physiol. 136: 3420–3426; 2004. doi:10.1104/pp.104.050351.
Washida H.; Sugina A.; Messing J.; Esen A.; Okita T. W. Asymmetric localization of seed storage protein RNAs to distinct subdomains of the endoplasmic reticulum in developing maize endosperm cells. Plant Cell Physiol. 45: 1830–1837; 2004 doi:10.1093/pcp/pch210.
Weeks J. T.; Anderson O. D.; Blechl A. E. Rapid production of multiple independent lines of fertile transgenic wheat (Triticum aestivum). Plant Physiol. 102: 1077–1084; 1993.
WHO. National strategies for overcoming micronutrient malnutrition. Geneva, Switzerland; 1992.
Wong J. H.; Kobrehel K.; Nimbona C.; Yee B. C.; Balogh A.; Kiss F.; Buchanan B. B. Thioredoxin and bread wheat. Cereal Chem. 70: 113–114; 1993.
Woo Y.-M.; Hu D. W.-N.; Larkins B. A.; Jung R. Genomics analysis of genes expressed in maize endosperm identifies novel seed proteins and clarifies patterns of zein gene expression. Plant Cell 13: 2297–2317; 2001.
Wood P. J. Cereal β-glucans in diet and health. J. Cereal Sci. 46: 230–238; 2007. doi:10.1016/j.jcs.2007.06.012.
Yamagata H.; Tanaka K. The site of synthesis and accumulation of rice storage proteins. Plant Cell Physiol. 27: 135–145; 1986.
Ye X.; Al-Babili S.; Kloti A.; Zhang J.; Lucca P.; Beyer P.; Potrykus I. Engineering the provitamin A (β-carotene) biosynthetic pathway into (carotenoid-free) rice endosperm. Science 287: 303–305; 2000. doi:10.1126/science.287.5451.303.
Yoshino Y.; Hayashi M.; Seguchi M. Presence and amounts of starch granule surface proteins in various starches. Cereal Chem. 82: 739–742; 2005. doi:10.1094/CC-82-0739.
Zhang Y.; Darlington H.; Jones H. D.; Halford N. G.; Napier J. A.; Davey M. R.; Lazzeri P. A.; Shewry P. R. Expression of the gamma-zein protein of maize in seeds of transgenic barley: effects on grain composition and properties. Theor. Appl. Genet. 106: 1139–1146; 2003.
Zhu T.; Budworth P.; Chen W. Q.; Provart N.; Chang H. S.; Guimil S.; Su W. P.; Estes B.; Zou G. Z.; Wang X. Transcriptional control of nutrient partitioning during rice grain filling. Plant Biotechnol. J. 1: 59–70; 2003. doi:10.1046/j.1467-7652.2003.00006.x.
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Godwin, I.D., Williams, S.B., Pandit, P.S. et al. Multifunctional grains for the future: genetic engineering for enhanced and novel cereal quality. In Vitro Cell.Dev.Biol.-Plant 45, 383–399 (2009). https://doi.org/10.1007/s11627-008-9175-5
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DOI: https://doi.org/10.1007/s11627-008-9175-5