FRET Response of a Modified Ribose Receptor Expressed in the Diatom Thalassiosira pseudonana [electronic resource]

• Ngôn ngữ: eng
• Ký hiệu phân loại: 580.1 Plants
• Thông tin xuất bản: Richland, Wash. : Oak Ridge, Tenn. : Pacific Northwest National Laboratory (U.S.) ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy, 2011
• Mô tả vật lý: Size: PDFN
• Bộ sưu tập: Metadata
• ID: 262328
• Chủ đề: 1. 59 basic biological sciences; 2. 60 applied life sciences; 3. Diatoms; 4. Enzymes; 5. Et al; 6. Fluorescence; 7. Functionals; 8. Proteins; 9. Receptors; 10. Ribose; 11. Silica

Tóm tắt

 The ability to insert complex proteins into silica has many applications including biosensing. Previous research has demonstrated how to direct proteins to the biosilica of diatoms [1]. Here, we show that a complex fusion protein that includes an enzyme, a bacterial ribose periplasmic binding protein, flanked by fluorescent proteins constituting a FRET pair can remain functional in the frustules of living diatoms. A Sil3 tag is attached to the N-terminal end to localize the fusion protein to frustules of the diatom Thalassiosira pseudonana. When ribose was applied, a larger decrease in FRET response was seen in transformed cells than in untransformed cells. Multiple forms of the expression vector were tested to find the optimal system
  specifically, a one-vector system was compared to a two-vector system and the gDNA version of the Sil3 localization tag was compared to the cDNA version. The optimal system was found to be a one-vector system with the genomic version of the Sil3 tag to direct the protein to the frustules. Localization of the enzyme to the frustules was further confirmed through cell fluorescence imaging.