Evidence map›Paper›PMID 41758383›Full record

ArticleTransgenic research2026

Targeted expression of Glycine max isoflavone synthase enhances daidzein and genistein content in soybean.

Nandakumar Vidya, Krishnagowdu Saravanan, Jayachandran Halka, Kumaresan Kowsalya, Packiaraj Gurusaravanan, Muthukrishnan Anand, Gomathi Selvavinayagam, Jesudass Joseph Sahayarayan, Muthukrishnan Arun

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Article in Transgenic research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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9 authors.

Nandakumar VidyaDepartment of Biotechnology, Bharathiar University, Coimbatore, Tamil Nadu, 641046, India.
Krishnagowdu SaravananDepartment of Biotechnology, Bharathiar University, Coimbatore, Tamil Nadu, 641046, India.
Jayachandran HalkaDepartment of Biotechnology, Bharathiar University, Coimbatore, Tamil Nadu, 641046, India.
Kumaresan KowsalyaDepartment of Biotechnology, Bharathiar University, Coimbatore, Tamil Nadu, 641046, India.
Packiaraj GurusaravananDepartment of Botany, Bharathiar University, Coimbatore, Tamil Nadu, 641046, India.
Muthukrishnan AnandRamco Institute of Technology, Rajapalayam, Tamil Nadu, 626117, India.
Gomathi SelvavinayagamRamco Institute of Technology, Rajapalayam, Tamil Nadu, 626117, India.
Jesudass Joseph SahayarayanDepartment of Bioinformatics, Alagappa University, Karaikudi, Tamil Nadu, 630003, India.
Muthukrishnan ArunDepartment of Biotechnology, Bharathiar University, Coimbatore, Tamil Nadu, 641046, India. arun@buc.edu.in.

Funding

Department of Science and Technology, Govt of India SR/WOS-A/LS-405/2018
6 · The paper itself

Abstract

Isoflavonoids are key secondary metabolites in leguminous plants that play essential roles in plant physiology and provide significant health benefits to humans. In the isoflavone biosynthetic pathway, isoflavone synthase (IFS) catalyzes the conversion of naringenin and liquiritigenin into the bioactive isoflavones genistein and daidzein. This study aimed to enhance genistein and daidzein accumulation in soybean seeds through genetic engineering. Agrobacterium tumefaciens strain EHA105 harboring the binary vector pCAMBIA1301 containing GmIFS under the control of a seed-specific promoter (Gmβ-conglycinin) was used to transform modified half-seed explants of soybean cv. JS335. Hygromycin-B-resistant plants were regenerated, hardened, and confirmed by histochemical GUS assay. Molecular analysis by PCR validated the presence of the GmIFS transgene, yielding a 700 bp amplicon. Biochemical analysis revealed that seeds of T₀ transgenic plants showed a 1.53-fold increase in total phenolic content and a 3.67-fold increase in flavonoid content compared to non-transformed controls. Antioxidant assays demonstrated significantly higher DPPH radical-scavenging activity and ferric-reducing antioxidant power (FRAP) in GmIFS-overexpressing plants. HPLC analysis further indicated that transgenic seeds accumulated, on average, 4.07-fold higher daidzein and 1.75-fold higher genistein levels relative to control plants. qRT-PCR analysis showed significantly elevated GmIFS expression in immature cotyledons, mature cotyledons, and seeds of transgenic plants. Overall, these results demonstrate that GmIFS overexpression effectively enhances isoflavone production in soybean seeds, highlighting the potential of metabolic engineering of biosynthetic pathway genes to improve nutritional quality.

Indexed as

GenisteinGlycine maxIsoflavonesOxygenasesPlants, Genetically ModifiedAgrobacterium tumefaciensGene Expression Regulation, PlantPromoter Regions, GeneticSeedsSeed Storage ProteinsSoybean ProteinsdaidzeinGenisteinIsoflavonesisoflavone synthaseOxygenasesSeed Storage ProteinsSoybean ProteinsGlycine maxIsoflavonesIsoflavone synthaseSoybean seedsTargeted expression

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.