Skip to main content

Corn

  • Chapter
  • First Online:

Abstract

Corn is an economic crop and serves as a staple and primary diet for large populations in many areas. Starch accounts for the largest constituent in corn, followed by protein, fiber, fat, and micronutrients such as vitamins and minerals. Zein protein is the major storage protein; however, zein is deficient in basic and acidic amino acids, especially lysine and tryptophan. In addition to providing macronutrients and micronutrients, corn also contains non-nutrient phytochemicals such as phenolic acids, anthocyanins, and carotenoids. The amount of specific phytochemicals in corn varies depending on genotypes and environmental factors. Overall, colorful corn such as blue and purple corns has more anthocyanins than yellow and white corn. Phenolic acids, anthocyanins, and carotenoids have shown many health benefits associated with lowering the risk of chronic diseases such as having anticancer, antihypertension, and anti-inflammation effects and preventing obesity. Dietary fiber in corn can also bring many health benefits such as weight control and gut health. However, the amount and bioavailability of micronutrients and non-nutrient phytochemicals in corn are relatively low. Heat processing results in the loss of vitamins and phytochemicals due to their low thermal stability. Hence, approaches such as fortification either in breeding or food processing have been applied for the purpose of increasing certain types of nutrient in food.

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD   109.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

References

  1. Micheletti AMS (2013) Carotenoids, Phenolic Compounds and Antioxidant Capacity of Five Local Italian Corn (Zea Mays L.) Kernels. J of Nutr Food Sci 3:6

    Google Scholar 

  2. Grain: World Markets and Trade (2019) ​USDA Foreign Agricultural Service gain report. 

    Google Scholar 

  3. Ranum P, Peñarosas JP, Garcia-Casal MN (2014) Global maize production, utilization, and consumption. Ann NY Acad Sci 1312:105

    PubMed  Google Scholar 

  4. Ai Y, Jane JL (2016) Macronutrients in corn and human nutrition. Compr Rev Food Sci Food Saf 15:581–598

    CAS  Google Scholar 

  5. Rausch K, Bergeron C, Carrier DJ, Ramaswamy S (2012) Phytochemicals from corn: a processing perspective. In: Biorefinery co-products: phytochemicals, primary metabolites and Value-added biomass processing, Wiley, Chichester, pp 55–92

    Google Scholar 

  6. Gwirtz JA, Garcia-Casal MN (2014) Processing maize flour and corn meal food products: Processing methods for staple maize food products. Ann NY Acad Sci 1312:66–75

    PubMed  PubMed Central  Google Scholar 

  7. Singh V, Johnston DB, Neoh SL (2010) Enzymatic corn wet milling process: enzyme optimization & commercial trial. Ind Biotechnol 6:34–40

    CAS  Google Scholar 

  8. Liu RH (2003) Health benefits of fruit and vegetables are from additive and synergistic combinations of phytochemicals. Am J Clin Nutr 78:517S

    CAS  PubMed  Google Scholar 

  9. Liu RH (2004) Potential synergy of phytochemicals in cancer prevention: mechanism of action. J Nutr 134:3479S

    CAS  PubMed  Google Scholar 

  10. Liu RH (2007) Whole grain phytochemicals and health. J Cereal Sci 46:207–219

    CAS  Google Scholar 

  11. Zhao Z, Egashira Y, Sanada H (2005) Phenolic antioxidants richly contained in corn bran are slightly bioavailable in rats. J Agric Food Chem 53:5030–5035

    CAS  PubMed  Google Scholar 

  12. Chanliaud E, Saulnier L, Thibault JF (1995) Alkaline extraction and characterisation of heteroxylans from maize bran. J Cereal Sci 21:195–203

    CAS  Google Scholar 

  13. Saulnier L, Vigouroux J, Thibault JF (1995) Isolation and partial characterization of feruloylated oligosaccharides from maize bran. Carbohydr Res 272:241–253

    CAS  PubMed  Google Scholar 

  14. Gani A, Wani SM, Masoodi FA, Hameed G (2012) Whole-grain cereal bioactive compounds and their health benefits: a review. J Food Process Technol 3:146

    Google Scholar 

  15. Adom KK, Liu RH (2002) Antioxidant activity of grains. J Agric Food Chem 50:6182–6187

    CAS  PubMed  Google Scholar 

  16. Vitaglione P, Napolitano A, Fogliano V (2008) Cereal dietary fibre: a natural functional ingredient to deliver phenolic compounds into the gut. Trends Food Sci Technol 19:451–463

    CAS  Google Scholar 

  17. Fetoni AR, Mancuso C, Eramo SLM, Ralli M, Piacentini R, Barone E et al (2010) In vivo protective effect of ferulic acid against noise-induced hearing loss in the Guinea-pig. Neuroscience 169:1575–1588

    CAS  PubMed  Google Scholar 

  18. Inns EL, Buggey LA, Booer C, Nursten HE, Ames JM (2011) Effect of modification of the kilning regimen on levels of free ferulic acid and antioxidant activity in malt. J Agric Food Chem 59:9335

    CAS  PubMed  Google Scholar 

  19. Trombino S, Cassano R, Ferrarelli T, Barone E, Picci N, Mancuso C (2013) Trans -ferulic acid-based solid lipid nanoparticles and their antioxidant effect in rat brain microsomes. Colloids Surf B Biointerfaces 109:273–279

    CAS  PubMed  Google Scholar 

  20. Janicke B, Hegardt C, Krogh M, Onning G, Akesson B, Cirenajwis HM et al (2011) The antiproliferative effect of dietary fiber phenolic compounds ferulic acid and p-coumaric acid on the cell cycle of Caco-2 cells. Nutr Cancer 63:611–622

    CAS  PubMed  Google Scholar 

  21. Li W, Li N, Tang Y, Li B, Liu L, Zhang X et al (2012) Biological activity evaluation and structure–activity relationships analysis of ferulic acid and caffeic acid derivatives for anticancer. Bioorg Med Chem Lett 22:6085–6088

    CAS  PubMed  Google Scholar 

  22. Kumar N, Kumar S, Abbat S, Nikhil K, Sondhi SM, Bharatam PV et al (2016) Ferulic acid amide derivatives as anticancer and antioxidant agents: synthesis, thermal, biological and computational studies. Med Chem Res 25:1175–1192

    CAS  Google Scholar 

  23. Panwar R, Sharma AK, Kaloti M, Dutt D, Pruthi V (2016) Characterization and anticancer potential of ferulic acid-loaded chitosan nanoparticles against ME-180 human cervical cancer cell lines. Appl Nanosci 6:803–813

    CAS  Google Scholar 

  24. Ardiansyah OY, Shirakawa H, Koseki T, Komai M (2008) Novel effects of a single Administration of Ferulic Acid on the regulation of blood pressure and the hepatic lipid metabolic profile in stroke-prone spontaneously hypertensive rats. J Agric Food Chem 56:2825–2830

    CAS  PubMed  Google Scholar 

  25. Alam MA, Sernia C, Brown L (2013) Ferulic acid improves cardiovascular and kidney structure and function in hypertensive rats. J Cardiovasc Pharmacol 61:240–249

    CAS  PubMed  Google Scholar 

  26. Sri BM, Rukkumani R, Menon VP (2003) Protective effects of ferulic acid on hyperlipidemic diabetic rats. Acta Diabetol 40:118–122

    Google Scholar 

  27. Naudi A, Jove M, Ayala V, Cassanye A, Serrano J, Gonzalo H et al (2012) Cellular dysfunction in diabetes as maladaptive response to mitochondrial oxidative stress. J Diabetes Res 2012:696215

    Google Scholar 

  28. Daglia M (2012) Polyphenols as antimicrobial agents. Curr Opin Biotechnol 23:174–181

    CAS  PubMed  Google Scholar 

  29. Borges A, Ferreira C, Saavedra MJ, Simões M (2013) Antibacterial activity and mode of action of ferulic and gallic acids against pathogenic bacteria. Microb Drug Resist 19:256–265

    CAS  PubMed  Google Scholar 

  30. Nile SH, Ko EY, Kim DH, Keum YS (2016) Screening of ferulic acid related compounds as inhibitors of xanthine oxidase and cyclooxygenase-2 with anti-inflammatory activity. Rev Bras 26:50–55

    CAS  Google Scholar 

  31. Doss HM, Dey C, Sudandiradoss C, Rasool MK (2016) Targeting inflammatory mediators with ferulic acid, a dietary polyphenol, for the suppression of monosodium urate crystal-induced inflammation in rats. Life Sci 148:201–210

    CAS  PubMed  Google Scholar 

  32. Zang LY, Cosma G, Gardner H, Shi X, Castranova V, Vallyathan V (2000) Effect of antioxidant protection by p-coumaric acid on low-density lipoprotein cholesterol oxidation. Am J Physiol Cell Physiol 279:954–960

    Google Scholar 

  33. Boz H (2015) p-Coumaric acid in cereals: presence, antioxidant and antimicrobial effects. Int J Food Sci Technol 50:2323–2328

    CAS  Google Scholar 

  34. Ekinci Akdemir FN, Albayrak M, Çalik M, Bayir Y, Gülçin İ (2017) The protective effects of p-Coumaric acid on acute liver and kidney damages induced by cisplatin. Biomedicine 5:18

    Google Scholar 

  35. Zhu H, Liang QH, Xiong XG, Wang Y, Zhang ZH, Sun MJ et al (2018) Anti-inflammatory effects of p-coumaric acid, a natural compound of oldenlandia diffusa, on arthritis model rats. Evid Based Complement Alternat Med 2018:1–9

    Google Scholar 

  36. Abdel-Aal ESM, Young JC, Rabalski I (2006) Anthocyanin composition in black, blue, pink, purple, and red cereal grains. J Agric Food Chem 54:4696–4704

    CAS  Google Scholar 

  37. Aoki H, Kuze N, Kato Y, Gen SE (2002) Anthocyanins isolated from purple corn (Zea mays L.). Foods Food Ingredients J Jpn 199:41–45

    Google Scholar 

  38. Salinas-Moreno Y, Martinez-Bustos F, Soto-Hernandez M, Ortega-Paczka R, Arellanovazquez JL (2003) Effect of alkaline cooking process on anthocyanins in pigmented maize grain. Agrociencia 37:617–628

    Google Scholar 

  39. Nankar AN, Dungan B, Paz N, Sudasinghe N, Schaub T, Holguin FO et al (2016) Quantitative and qualitative evaluation of kernel anthocyanins from southwestern United States blue corn. J Sci Food Agric 96:4542

    CAS  PubMed  Google Scholar 

  40. Bowen-Forbes CS, Zhang Y, Nair MG (2010) Anthocyanin content, antioxidant, anti-inflammatory and anticancer properties of blackberry and raspberry fruits. J Food Compos Anal 23:554–560

    CAS  Google Scholar 

  41. Benvenuti S, Bortolotti E, Maggini R (2016) Antioxidant power, anthocyanin content and organoleptic performance of edible flowers. Sci Hortic 199:170–177

    CAS  Google Scholar 

  42. Long N, Suzuki S, Sato S, Naiki-Ito A, Sakatani K, Shirai T et al (2013) Purple corn color inhibition of prostate carcinogenesis by targeting cell growth pathways. Cancer Sci 104:298–303

    CAS  PubMed  Google Scholar 

  43. Lim S, Xu J, Kim J, Chen TY, Su X, Standard J et al (2013) Role of anthocyanin-enriched purple-fleshed sweet potato p40 in colorectal cancer prevention. Mol Nutr Food Res 57:1908–1917

    CAS  PubMed  PubMed Central  Google Scholar 

  44. Charepalli V, Reddivari L, Radhakrishnan S, Vadde R, Agarwal R, Vanamala JKP (2015) Anthocyanin-containing purple-fleshed potatoes suppress colon tumorigenesis via elimination of colon cancer stem cells. J Nutr Biochem 26:1641–1649

    CAS  PubMed  Google Scholar 

  45. Kazan A, Sevimli-Gur C, Yesil-Celiktas O, Dunford NT (2016) Investigating anthocyanin contents and in vitro tumor suppression properties of blueberry extracts prepared by various processes. Eur Food Res Technol 242:693–701

    CAS  Google Scholar 

  46. Li JT, Zhang JL, He H, Ma ZL, Nie ZK, Wang ZZ et al (2013) Apoptosis in human hepatoma HepG2 cells induced by corn peptides and its anti-tumor efficacy in H22 tumor bearing mice. Food Chem Toxicol 51:297–305

    CAS  PubMed  Google Scholar 

  47. Rojo LE, Ribnicky D, Logendra S, Poulev A, Rojas-Silva P, Kuhn P et al (2012) In vitro and in vivo anti-diabetic effects of anthocyanins from Maqui berry (Aristotelia chilensis). Food Chem 131:387

    CAS  PubMed  Google Scholar 

  48. Güdr A (2016) Influence of Total anthocyanins from bitter melon (Momordica charantia Linn.) as antidiabetic and radical scavenging agents. Iran J Pharm Res 15:301

    PubMed  PubMed Central  Google Scholar 

  49. Lee C, Han D, Kim B, Baek N, Baik BK (2013) Antioxidant and anti-hypertensive activity of anthocyanin-rich extracts from hulless pigmented barley cultivars. Int J Food Sci Technol 48:984–991

    CAS  Google Scholar 

  50. Patil BS, Jayaprakasha GK, Murthy KNC, Vikram A (2009) Bioactive compounds: historical perspectives, opportunities, and challenges. J Agric Food Chem 57:8142–8160

    CAS  PubMed  Google Scholar 

  51. Schoefs BT (2003) Chlorophyll and carotenoid analysis in food products. A practical case-by-case view. TrAC Trends Anal Chem 22:335–339

    CAS  Google Scholar 

  52. Kurilich AC, Juvik JA (1999) Quantification of carotenoid and tocopherol antioxidants in Zea mays. J Agric Food Chem 47:1948–1955

    CAS  PubMed  Google Scholar 

  53. Wurtzel ET, Cuttriss A, Vallabhaneni R (2012) Maize Provitamin A Carotenoids, current resources, and future metabolic engineering challenges. Front Plant Sci 3:29

    PubMed  PubMed Central  Google Scholar 

  54. Loy DD, Wright KN, White PJ, Johnson LA (1987) Nutritional properties and feeding value of corn and its by-products. Corn Chem Technol

    Google Scholar 

  55. Watson SA, Ramstad PE (1987) Measurement and maintenance of quality. Corn Chem Technol

    Google Scholar 

  56. Moros EE, Darnoko D, Cheryan M, Perkins EG, Jerrell J (2002) Analysis of xanthophylls in corn by HPLC. J Agric Food Chem 50:5787–5790

    CAS  PubMed  Google Scholar 

  57. Sluijs I, Cadier E, Beulens JWJ, Van der ADL, Spijkerman AMW, Schouw YTVD (2015) Dietary intake of carotenoids and risk of type 2 diabetes. Nutr Metab Cardiovasc Dis 25:376–381

    CAS  PubMed  Google Scholar 

  58. Roohbakhsh A, Karimi G, Iranshahi M (2017) Carotenoids in the treatment of diabetes mellitus and its complications: a mechanistic review. Biomed Pharmacother 91:31

    CAS  PubMed  Google Scholar 

  59. Chung RWS, Leanderson P, Lundberg AK, Jonasson L (2017) Lutein exerts anti-inflammatory effects in patients with coronary artery disease. Atherosclerosis 262:87

    CAS  PubMed  Google Scholar 

  60. Song B, Liu K, Gao Y, Zhao L, Fang H, Li Y et al (2017) Lycopene and risk of cardiovascular diseases: a meta-analysis of observational studies. Mol Nutr Food Res 2017:1601009

    Google Scholar 

  61. Lowe GM, Booth LA, Young AJ, Bilton RF (1999) Lycopene and beta-carotene protect against oxidative damage in HT29 cells at low concentrations but rapidly lose this capacity at higher doses. Free Radic Res 30:141–151

    CAS  PubMed  Google Scholar 

  62. Sajjadi M, Bathaie Z (2017) Comparative study on the preventive effect of saffron Carotenoids, Crocin and Crocetin, in NMU-induced breast Cancer in rats. Cell J 19:94–101

    PubMed  Google Scholar 

  63. Zhang X, Zhao WE, Hu L, Zhao L, Huang J (2011) Carotenoids inhibit proliferation and regulate expression of peroxisome proliferators-activated receptor gamma (PPARγ) in K562 cancer cells. Arch Biochem Biophys 512:96–106

    CAS  PubMed  Google Scholar 

  64. Hernández-Ortega M, Ortiz-Moreno A, Hernández-Navarro MD, Chamorro-Cevallos G, Dorantes-Alvarez L, Necoechea-Mondragón H (2012) Antioxidant, antinociceptive, and anti-inflammatory effects of carotenoids extracted from dried pepper (Capsicum annuum L.). Biomed Res Int 2012:524019

    Google Scholar 

  65. Johnson EJ (2002) The role of carotenoids in human health. Nutr Clin Care 5:56–65

    PubMed  Google Scholar 

  66. Stringham JM, Stringham NT, O’Brien KJ (2017) Macular carotenoid supplementation improves visual performance, sleep quality, and adverse physical symptoms in those with high screen time exposure. Foods 6:47

    PubMed Central  Google Scholar 

  67. Duffield-Lillico AJ, Begg CB (2004) Reflections on the landmark studies of beta-carotene supplementation. J Natl Cancer Inst 96:1729

    CAS  PubMed  Google Scholar 

  68. Sun Z, Yao H (2007) The influence of di-acetylation of the hydroxyl groups on the anti-tumor-proliferation activity of lutein and zeaxanthin. Asia Pac J Clin Nutr 16:447–452

    CAS  PubMed  Google Scholar 

  69. Howe JA, Tanumihardjo SA (2006) Evaluation of analytical methods for carotenoid extraction from biofortified maize (Zea mays sp.). J Agric Food Chem 54:7992–7997

    CAS  PubMed  Google Scholar 

  70. Ye J, Feng L, Xiong J, Xiong Y (2011) Ultrasound-assisted extraction of corn carotenoids in ethanol. Int J Food Sci Technol 46:2131–2136

    CAS  Google Scholar 

  71. Ishida BK, Chapman MH (2009) Carotenoid extraction from plants using a novel, environmentally friendly solvent. J Agric Food Chem 57:1051–1059

    CAS  PubMed  Google Scholar 

  72. Lu Y, Yao H, Gong Y, Sheng Q (2005) Effects of enzymatic treatment of corn gluten meal on lutein and zeaxanthin extraction. Int J Food Prop 8:161–169

    CAS  Google Scholar 

  73. Badami S, Manohara RSA, Kumar EP, Vijayan P, Suresh B (2003) Antitumor activity of total alkaloid fraction of solanum pseudocapsicum leaves. Phytother Res 17:1001–1004

    PubMed  Google Scholar 

  74. Zhang Y, Li X, Zou D, Liu W, Yang J, Zhu N et al (2008) Treatment of type 2 diabetes and dyslipidemia with the natural plant alkaloid berberine. J Clin Endocrinol Metab 93:2559–2565

    CAS  PubMed  Google Scholar 

  75. Owoyele BV, Negedu MN, Olaniran SO, Onasanwo SA, Oguntoye SO, Sanya JO et al (2010) Analgesic and anti-inflammatory effects of aqueous extract of Zea mays husk in male Wistar rats. J Med Food 13:343

    PubMed  Google Scholar 

  76. Thoudam B, Kirithika T, Ramya J, Usha K (2011) Phytochemical constituents and antioxidant activity of various extracts of corn silk (Zea mays L). Res J Pharm Biol Chem Sci 2:986–993

    Google Scholar 

  77. Solihah MA, Wan Rosli WI, Nurhanan AR (2012) Phytochemicals screening and total phenolic content of Malaysian Zea mays hair extracts. Int Food Res J 2012:1533–1538

    Google Scholar 

  78. Ahmed HM (2017) Phytochemical screening, total phenolic content and phytotoxic activity of corn (Zea mays) extracts against some indicator species. Nat Prod Res 32:1

    Google Scholar 

  79. Shukla R, Cheryan M (2001) Zein: the industrial protein from corn. Ind Crop Prod 13:171–192

    CAS  Google Scholar 

  80. Wang L, Xu C, Qu M, Zhang J (2008) Kernel amino acid composition and protein content of introgression lines from Zea mays ssp. mexicana into cultivated maize. J Cereal Sci 48:387–393

    CAS  Google Scholar 

  81. Geraghty DE, Messing J, Rubenstein I (1982) Sequence analysis and comparison of cDNAs of the zein multigene family. EMBO J 1:1329

    CAS  PubMed  PubMed Central  Google Scholar 

  82. Esen A (1987) A proposed nomenclature for the alcohol-soluble proteins (Zeins) of maize (Zea mays L.). J Cereal Sci 5:117–128

    CAS  Google Scholar 

  83. Pomes AF (2014) Encyclopedia of polymer science and technology, 4th edn. Wiley, Hoboken

    Google Scholar 

  84. Wang XJ, Zheng XQ, Kopparapu NK, Cong WS, Deng YP, Sun XJ et al (2014) Purification and evaluation of a novel antioxidant peptide from corn protein hydrolysate. Process Biochem 49:1562–1569

    CAS  Google Scholar 

  85. Jin DX, Liu XL, Zheng XQ, Wang XJ, He JF (2016) Preparation of antioxidative corn protein hydrolysates, purification and evaluation of three novel corn antioxidant peptides. Food Chem 204:427

    CAS  PubMed  Google Scholar 

  86. Mochida T, Hira T, Hara H (2010) The corn protein, zein hydrolysate, administered into the ileum attenuates hyperglycemia via its dual action on glucagon-like peptide-1 secretion and dipeptidyl peptidase-IV activity in rats. Endocrinology 151:3095

    CAS  PubMed  Google Scholar 

  87. Zou TB, He TP, Li HB, Tang HW, Xia EQ (2016) The structure-activity relationship of the antioxidant peptides from natural proteins. Molecules 21:72

    PubMed  PubMed Central  Google Scholar 

  88. Díaz-Gómez JL, Castorenatorres F, Preciadoortiz RE, Garcíalara S (2017) Anti-Cancer activity of maize bioactive peptides. Front Chem 5:4

    Google Scholar 

  89. Zhou C, Hu J, Ma H, Yagoub AE, Yu X, Owusu J et al (2015) Antioxidant peptides from corn gluten meal: orthogonal design evaluation. Food Chem 187:270–278

    CAS  PubMed  Google Scholar 

  90. Lin F, Chen L, Liang R, Zhang Z, Wang J, Cai M et al (2011) Pilot-scale production of low molecular weight peptides from corn wet milling byproducts and the antihypertensive effects in vivo and in vitro. Food Chem 124:801–807

    CAS  Google Scholar 

  91. Jiang HX, Lio JY, Blanco M, Campbell M, Jane JL (2010) Resistant-starch formation in high-amylose maize starch during kernel development. J Agric Food Chem 58:8043–8047

    CAS  PubMed  Google Scholar 

  92. Murphy MM, Douglass JS, Birkett A (2008) Resistant starch intakes in the United States. J Am Diet Assoc 108:67–78

    PubMed  Google Scholar 

  93. Mutlu S, Kahraman K (2017) S Ö. Optimization of resistant starch formation from high amylose corn starch by microwave irradiation treatments and characterization of starch preparations. Int J Biol Macromol 95:635–642

    CAS  PubMed  Google Scholar 

  94. Luckett CR, Wang YJ (2012) Effects of β-amylolysis on the resistant starch formation of debranched corn starches. J Agric Food Chem 60:4751

    CAS  PubMed  Google Scholar 

  95. Zhou X, Chung HJ, Kim JY, Lim ST (2013) In vitro analyses of resistant starch in retrograded waxy and normal corn starches. Int J Biol Macromol 55:113–117

    CAS  PubMed  Google Scholar 

  96. Papathanasiou MM, Reineke K, Gogou E, Taoukis PS, Knorr D (2015) Impact of high pressure treatment on the available glucose content of various starch types: a case study on wheat, tapioca, potato, corn, waxy corn and resistant starch (RS3). Innov Food Sci Emerg Technol 30:24–30

    CAS  Google Scholar 

  97. Ludwig DS (2000) Dietary glycemic index and obesity. J Nutr 130:280S

    CAS  PubMed  Google Scholar 

  98. Wang X, Brown IL, Khaled D, Mahoney MC, Evans AJ, Conway PL (2002) Manipulation of colonic bacteria and volatile fatty acid production by dietary high amylose maize (amylomaize) starch granules. J Appl Microbiol 93:390–397

    CAS  PubMed  Google Scholar 

  99. Higgins JA, Higbee DR, Donahoo WT, Brown IL, Bell ML, Bessesen DH (2004) Resistant starch consumption promotes lipid oxidation. Nutr Metab 1:1–11

    Google Scholar 

  100. Chung HJ, Liu Q, Hoover Q (2009) Impact of annealing and heat-moisture treatment on rapidly digestible, slowly digestible and resistant starch levels in native and gelatinized corn, pea and lentil starches. Carbohydr Polym 75:436–447

    CAS  Google Scholar 

  101. Otten JJ, Hellwig JP, Meyers LD, Medicine IODRI (2006) Dietary reference intakes: the essential guide to nutrient requirements. Am J Clin Nutr 85:924

    Google Scholar 

  102. De Moura FF, Miloff A, Boy E (2015) Retention of Provitamin a carotenoids in staple crops targeted for biofortification in Africa: cassava, maize and sweet potato. C R C. Crit Rev Food Technol 55:1246–1269

    Google Scholar 

  103. Rocheford TR, Wong JC, Egesel CO, Lambert RJ (2002) Enhancement of vitamin E levels in corn. J Am Coll Nutr 21:191S–198S

    CAS  PubMed  Google Scholar 

  104. Ferland G, Sadowski JA (1992) Vitamin K1 (phylloquinone) content of edible oils: effects of heating and light exposure. J Agric Food Chem 40:1869–1873

    CAS  Google Scholar 

  105. Suri DJ, Tanumihardjo SA (2016) Effects of different processing methods on the micronutrient and phytochemical contents of maize: from A to Z. Compr Rev Food Sci Food Saf 15:912–926

    CAS  Google Scholar 

  106. Biswas M, Haldar PK, Ghosh AK (2010) Antioxidant and free-radical-scavenging effects of fruits of Dregea volubilis. J Nat Sci Biol Med 1:29–34

    PubMed  PubMed Central  Google Scholar 

  107. Slavin JL (2005) Dietary fiber and body weight. Nutrition 21:411–418

    PubMed  Google Scholar 

  108. Brighenti F, Benini L, Del Rio D, Casiraghi C, Pellegrini N, Scazzina F, Jenkins DJ et al (2006) Colonic fermentation of indigestible carbohydrates contributes to the second-meal effect. Am J Clin Nutr 83:817–822

    CAS  PubMed  Google Scholar 

  109. Gemen R, Vries JFD, Slavin JL (2011) Relationship between molecular structure of cereal dietary fiber and health effects: focus on glucose/insulin response and gut health. Nutr Rev 69:22–33

    PubMed  Google Scholar 

  110. Hoebler C, Karinthi A, Chiron H, Champ M, Barry JL (1999) Bioavailability of starch in bread rich in amylose : metabolic responses in healthy subjects and starch structure. Eur J Clin Nutr 53:360–366

    CAS  PubMed  Google Scholar 

  111. Gibson GR, Roberfroid MB (1995) Dietary modulation of the human colonic microbiota: introducing the concept of prebiotics. J Nutr 17:1401–1412

    Google Scholar 

  112. Johnston DB, Mcaloon AJ, Moreau RA, Hicks KB, Singh V (2005) Composition and economic comparison of germ fractions from modified corn processing technologies. J Am Oil Chem Soc 82:603–608

    CAS  Google Scholar 

  113. Mamatha BS, Arunkumar R, Baskaran V (2012) Effect of processing on major carotenoid levels in corn (Zea mays) and selected vegetables: bioavailability of lutein and zeaxanthin from processed corn in mice. Food Bioprocess Technol 5:1355–1363

    CAS  Google Scholar 

  114. Maya-Cortés DC, Cárdenas JDDF, Garnica-Romo MG, Cuevas-Villanueva RA, Cortés-Martínez R, Véles-Medina JJ et al (2010) Whole-grain corn tortilla prepared using an ecological nixtamalisation process and its impact on the nutritional value. Int J Food Sci Technol 45:23–28

    Google Scholar 

  115. Parra CDL, Saldivar SOS, Liu RH (2007) Effect of processing on the phytochemical profiles and antioxidant activity of corn for production of masa, tortillas, and tortilla chips. J Agric Food Chem 55:4177–4183

    PubMed  Google Scholar 

  116. Maya-Cortés DC, Cárdenas F, de Dios J, Garnica-Romo M, Cuevas-Villanueva RA, Cortés-Martínez R , Martínez-Flores HE (2010) Whole grain corn tortilla prepared using an ecological nixtamalisation process and its impact on the nutritional value. Int J Food Scie tech 45:1

    Google Scholar 

  117. Kandil A, Li J, Vasanthan T, Bressler DC, Tyler RT (2011) Compositional changes in whole grain flours as a result of solvent washing and their effect on starch amylolysis. Food Res Int 44:167–173

    CAS  Google Scholar 

  118. Korus J, Gumul D, Czechowska K (2007) Effect of extrusion on the phenolic composition and antioxidant activity of dry beans of Phaseolus vulgaris L. Food Technol Biotechnol 45:139–146

    Google Scholar 

  119. Riaz MN, Asif M, Ali R (2009) Stability of vitamins during extrusion. Crit Rev Food Sci Nutr 49:361–368

    CAS  PubMed  Google Scholar 

  120. Altan A, Mccarthy KL, Maskan M (2009) Effect of extrusion process on antioxidant activity, total phenolics and β-glucan content of extrudates developed from barley-fruit and vegetable by-products. Int J Food Sci Technol 44:1263–1271

    CAS  Google Scholar 

  121. White BL, Howard LR, Prior RL (2010) Polyphenolic composition and antioxidant capacity of extruded cranberry pomace. J Agric Food Chem 58:4037–4042

    CAS  PubMed  Google Scholar 

  122. Ortiz-Monasterio JI, Palacios-Rojas N, Meng E, Pixley K, Trethowan R, Peña RJ (2007) Enhancing the mineral and vitamin content of wheat and maize through plant breeding. J Cereal Sci 46:293–307

    CAS  Google Scholar 

  123. Naqvi S, Zhu C, Farre G, Ramessar K, Bassie L, Breitenbach J et al (2009) Transgenic multivitamin corn through biofortification of endosperm with three vitamins representing three distinct metabolic pathways. Proc Natl Acad Sci USA 106:7762–7767

    CAS  PubMed  Google Scholar 

  124. Wu F (2006) Mycotoxin reduction in Bt corn: potential economic, health, and regulatory impacts. Transgenic Res 15:277–289

    PubMed  Google Scholar 

  125. Monnard A, Moretti D, Zeder C, Steingötter A, Zimmermann MB (2017) The effect of lipids, a lipid-rich ready-to-use therapeutic food, or a phytase on iron absorption from maize-based meals fortified with micronutrient powders. Am J Clin Nutr 105:1521–1527

    CAS  PubMed  Google Scholar 

  126. Moretti D, Biebinger R, Bruins MJ, Hoeft B, Kraemer K (2014) Bioavailability of iron, zinc, folic acid, and vitamin a from fortified maize. Ann NY Acad Sci 1312:54–65

    CAS  PubMed  Google Scholar 

  127. Ho TY, Li CC, Lo HY, Chen FY, Hsiang CY (2017) Corn silk extract and its bioactive peptide ameliorated lipopolysaccharide-induced inflammation in mice via the nuclear factor-κB signaling pathway. J Agric Food Chem 65:759

    CAS  PubMed  Google Scholar 

  128. Guo H, Guan H, Yang W, Liu H, Hou H, Chen X et al (2017) Pro-apoptotic and anti-proliferative effects of corn silk extract on human colon cancer cell lines. Oncol Lett 13:973

    PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgments

This is contribution no. 18-622-B from the Kansas Agricultural Experimental Station.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yonghui Li .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2019 Springer Nature Singapore Pte Ltd.

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Xu, J., Li, Y., Wang, W. (2019). Corn. In: Wang, J., Sun, B., Tsao, R. (eds) Bioactive Factors and Processing Technology for Cereal Foods. Springer, Singapore. https://doi.org/10.1007/978-981-13-6167-8_3

Download citation

Publish with us

Policies and ethics