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Gene Synthesis> | DNA fragments encoding Pifuc-TM-1 or Pifuc-TM-2, with codon usage optimized for expression in Escherichia coli, were commercially synthesized by GenScript Gene Synthesis Service (GenScript, Piscataway, NJ, USA) and inserted into the T7 expression vector pET21b (Novagen Darmstadt, Germany). To mimic acetylation, alanine and serine residues were added to the N-terminus. E. coli BL21(DE3) transformed with pET-Pifuc-TM-1 or pET-Pifuc-TM-2 was cultured in auto-induction media at 37˚C for 24 h [17]. The E. coli cultures were collected by centrifugation and suspended in a lysis buffer included in the EzBactYeast Crusher kit (ATTO, Tokyo, Japan). Supernatants of the lysates obtained by centrifugation containing Pifuc-TM-1 or Pifuc-TM-2 were subjected to ion-exchange chromatography on a TSK-gel DEAE-5PW column (7.5 × 75 mm) (Tosoh, Tokyo, Japan) after dialysis against 50 mM Tris-HCl (pH 7.5) containing 30 mM KCl and 0.1 mM DTT. The proteins were eluted with a linear gradient of 30 mM to 600 mM KCl. | Get A Quote |
We determined the full-length primary structure of the tropomyosin (TM)-1 and -2 proteins from the adductor muscle of the Japanese pearl oyster Pinctada fucata (Pifuc-TM-1 and Pifuc-TM-2), and found that they are each composed of 284 amino acid residues. We predicted the gene structure of P. fucataTM (Pifuc-TM) using Splign alignment of our cDNA with genomic sequences and elucidated that Pifuc-TM consists of 10 exons. Exons 1 - 3 and 5 - 10 are used to transcribe Pifuc-TM-1 mRNA, and exons 1 - 4 and 6 - 10 are used to transcribe Pifuc-TM-2 mRNA. Both genes share the same start and stop codons located in exon 1 and exon 10, respectively. Using quantitative real-time PCR, we determined that the Pifuc-TM... More