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Comparative investigation of seed coats of brown- versus yellow-colored soybean seeds using an integrated proteomics and metabolomics approach.
Gupta, Ravi; Min, Chul Woo; Kim, So Wun; Wang, Yiming; Agrawal, Ganesh Kumar; Rakwal, Randeep; Kim, Sang Gon; Lee, Byong Won; Ko, Jong Min; Baek, In Yeol; Bae, Dong Won; Kim, Sun Tae.
Affiliation
  • Gupta R; Department of Plant Bioscience, College of Natural Resources and Life Sciences, Pusan National University, Miryang, South Korea.
  • Min CW; Department of Plant Bioscience, College of Natural Resources and Life Sciences, Pusan National University, Miryang, South Korea.
  • Kim SW; Department of Plant Bioscience, College of Natural Resources and Life Sciences, Pusan National University, Miryang, South Korea.
  • Wang Y; Department of Plant Microbe Interaction, Max Planck Institute for Plant Breeding Research, Cologne, Germany.
  • Agrawal GK; Research Laboratory for Biotechnology and Biochemistry (RLABB), Kathmandu, Nepal.
  • Rakwal R; GRADE Academy Private Limited, Birgunj, Nepal.
  • Kim SG; Research Laboratory for Biotechnology and Biochemistry (RLABB), Kathmandu, Nepal.
  • Lee BW; GRADE Academy Private Limited, Birgunj, Nepal.
  • Ko JM; Organization for Educational Initiatives, University of Tsukuba, Tsukuba, Ibaraki, Japan.
  • Baek IY; Department of Anatomy I, Showa University School of Medicine, Shinagawa, Tokyo, Japan.
  • Bae DW; Plant Molecular Biology and Biotechnology Research Center, Gyeongsang National University, Jinju, South Korea.
  • Kim ST; Department of Functional Crops, NICS, RDA, Miryang, South Korea.
Proteomics ; 15(10): 1706-16, 2015 May.
Article in En | MEDLINE | ID: mdl-25545850
ABSTRACT
Seed coat color is an important attribute determining consumption of soybean seeds. Soybean cultivar Mallikong (M) has yellow seed coat while its naturally mutated cultivar Mallikong mutant (MM), has brown colored seed coat. We used integrated proteomics and metabolomics approach to investigate the differences between seed coats of M and MM during different stages of seed development (4, 5, and 6 weeks after flowering). 2DE profiling of total seed coat proteins from three stages showed 178 differentially expressed spots between M and MM of which 172 were identified by MALDI-TOF/TOF. Of these, 62 were upregulated and 105 were downregulated in MM compared with M, while five spots were detected only in MM. Proteins involved in primary metabolism showed downregulation in MM suggesting energy in MM might be utilized for proanthocyanidin biosynthesis via secondary metabolic pathways that leads to the development of brown seed coat color. Besides, downregulation of two isoforms of isoflavone reductase indicated reduced isoflavones in seed coat of MM that was confirmed by quantitative estimation of total and individual isoflavones using HPLC. We propose that low isoflavones level in MM may offer a high substrate for proanthocyanidin production that results in the development of brown seed coat in MM.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seeds / Glycine max / Pigmentation / Proteomics / Metabolomics Language: En Journal: Proteomics Journal subject: BIOQUIMICA Year: 2015 Document type: Article Affiliation country: Corea del Sur

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seeds / Glycine max / Pigmentation / Proteomics / Metabolomics Language: En Journal: Proteomics Journal subject: BIOQUIMICA Year: 2015 Document type: Article Affiliation country: Corea del Sur