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Functional characterization and differential expression studies of squalene synthase from Withania somnifera
- Gupta, Neha, Sharma, Poonam, Santosh Kumar, R. J., Vishwakarma, Rishi K., Khan, B. M.
- Molecular biology reports 2012 v.39 no.9 pp. 8803-8812
- Capsicum annuum, Escherichia coli, Nicotiana tabacum, Solanum tuberosum, Withania somnifera, affinity chromatography, amino acid sequences, amino acids, biosynthesis, carbon, clones, complementary DNA, enzyme activity, enzymes, gas chromatography-mass spectrometry, gene expression regulation, hydrophobicity, isoprenoids, leaves, open reading frames, polyacrylamide gel electrophoresis, polypeptides, quantitative polymerase chain reaction, recombinant proteins, reverse transcriptase polymerase chain reaction
- Squalene synthase (SQS: EC 220.127.116.11) is a potential branch point regulatory enzyme and represents the first committed step to diverge the carbon flux from the main isoprenoid pathway towards sterol biosynthesis. In the present study, cloning and characterization of Withania somnifera squalene synthase (WsSQS) cDNA was investigated subsequently followed by its heterologous expression and preliminary enzyme activity. Two different types of WsSQS cDNA clones (WsSQS1and WsSQS2) were identified that contained an open reading frames of 1,236 and 1,242 bp encoding polypeptides of 412 and 414 amino acids respectively. Both WsSQS isoforms share 99 % similarity and identity with each other. WsSQS deduced amino acids sequences, when compared with SQS of other plant species, showed maximum similarity and identity with Capsicum annuum followed by Solanum tuberosum and Nicotiana tabacum. To obtain soluble recombinant enzymes, 24 hydrophobic amino acids were deleted from the carboxy terminus and expressed as 6X His–Tag fusion protein in Escherichia coli. Approximately 43 kDa recombinant protein was purified using Ni–NTA affinity chromatography and checked on SDS-PAGE. Preliminary activity of the purified enzymes was determined and the products were analyzed by gas chromatograph–mass spectrometer (GC–MS). Quantitative real-time PCR (qRT-PCR) analysis showed that WsSQS expresses more in young leaves than mature leaves, stem and root.