Influence of Human Lactoferrin Expression on Iron Homeostasis, Flavonoids, and Antioxidants in Transgenic Tobacco

被引:6
作者
Kumar, Vinay [1 ]
Gill, Tejpal [1 ]
Grover, Sunita [2 ]
Ahuja, Paramvir Singh [1 ]
Yadav, Sudesh Kumar [1 ]
机构
[1] CSIR, Inst Himalayan Bioresource Technol, Div Biotechnol, Palampur 176061, Himachal Prades, India
[2] Natl Dairy Res Inst, Dairy Microbiol Div, Mol Biol Unit, Karnal 132001, Haryana, India
关键词
Antioxidants; Human lactoferrin; Total flavonoids; Iron homeostasis; RECOMBINANT HUMAN LACTOFERRIN; FE(III) CHELATE REDUCTASE; OXIDATIVE STRESS; ARABIDOPSIS; GENE; METHYLGLYOXAL; ACCUMULATION; GLUTATHIONE; ASCORBATE; ENZYMES;
D O I
10.1007/s12033-012-9495-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study was aimed at to check the influence of human lactoferrin (hLF) expression on iron homeostasis, flavonoids, and antioxidants in transgenic tobacco. Transgenic tobacco expressing hLF cDNA under the control of a CaMV 35S promoter was produced. The iron content as well as chlorophyll content of transgenic tobacco was lower compared to mock and untransformed wild plants. Interestingly, hLF transgenic tobacco showed higher level of transcript expression for genes related to iron content regulation like iron transporter and metal transporter. While expression of genes related to iron storage such as ferritin 1 and ferritin 2 was downregulated. The transcript expression of genes encoding antioxidant enzymes such as glutathione reductase, glutathione-S-transferase, ascorbate peroxidase, and catalase was downregulated in hLF transgenic tobacco compared to controls. Further, the transcript expression of two important genes encoding dihydroflavonol reductase (DFR) and phenylalanine ammonia lyase regulatory enzymes of flavonoid biosynthesis pathway was analyzed. The expression of DFR was found to be downregulated, while PAL expression was upregulated in hLF transgenic tobacco compared to mock and untransformed wild plant. Total phenolics, flavonoids, and proanthocyanidins contents were found to be higher in hLF transgenic tobacco than the mock and untransformed wild plant. Results suggest that hLF expression in transgenic tobacco leads to iron deficiency, downregulation of antioxidant enzymes, and increase in total flavonoids.
引用
收藏
页码:118 / 128
页数:11
相关论文
共 40 条
[1]   Lactoferrin: a review [J].
Adlerova, L. ;
Bartoskova, A. ;
Faldyna, M. .
VETERINARNI MEDICINA, 2008, 53 (09) :457-468
[2]   Evolution and current status of research in phenolic compounds [J].
Boudet, Alain-Michel .
PHYTOCHEMISTRY, 2007, 68 (22-24) :2722-2735
[3]   Ferritins and iron storage in plants [J].
Briat, Jean-Francois ;
Duc, Celine ;
Ravet, Karl ;
Gaymard, Frederic .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2010, 1800 (08) :806-814
[4]   High-Affinity Manganese Uptake by the Metal Transporter NRAMP1 Is Essential for Arabidopsis Growth in Low Manganese Conditions [J].
Cailliatte, Remy ;
Schikora, Adam ;
Briat, Jean-Francois ;
Mari, Stephane ;
Curie, Catherine .
PLANT CELL, 2010, 22 (03) :904-917
[5]   High expression of a human lactoferrin in transgenic tobacco cell cultures [J].
Choi, SM ;
Lee, OS ;
Kwon, SY ;
Kwak, SS ;
Yu, DY ;
Lee, HS .
BIOTECHNOLOGY LETTERS, 2003, 25 (03) :213-218
[6]   Recombinant human lactoferrin: A valuable protein for pharmaceutical products and functional foods [J].
Conesa, Celia ;
Calvo, Miguel ;
Sanchez, Lourdes .
BIOTECHNOLOGY ADVANCES, 2010, 28 (06) :831-838
[7]   Involvement of NRAMP1 from Arabidopsis thaliana in iron transport [J].
Curie, C ;
Alonso, JM ;
Le Jean, M ;
Ecker, JR ;
Briat, JF .
BIOCHEMICAL JOURNAL, 2000, 347 (pt 3) :749-755
[8]   Siderophore-mediated upregulation of Arabidopsis ferritin expression in response to Erwinia chrysanthemi infection [J].
Dellagi, A ;
Rigault, M ;
Segond, D ;
Roux, C ;
Kraepiel, Y ;
Cellier, F ;
Briat, JF ;
Gaymard, F ;
Expert, D .
PLANT JOURNAL, 2005, 43 (02) :262-272
[9]   Ectopic expression of nicotianamine synthase genes results in improved iron accumulation and increased nickel tolerance in transgenic tobacco [J].
Douchkov, D ;
Gryczka, C ;
Stephan, UW ;
Hell, R ;
Bäumlein, H .
PLANT CELL AND ENVIRONMENT, 2005, 28 (03) :365-374
[10]  
Ebrahimzadeh MA, 2008, AFR J BIOTECHNOL, V7, P3188