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Single live-bacterial cell assay of promoter activity and regulation

  • Jun Teramoto
  • , Yoko Yamanishi
  • , El Shimy H. Magdy
  • , Akiko Hasegawa
  • , Ayako Kori
  • , Masahiro Nakajima
  • , Fumihito Arai
  • , Toshio Fukuda
  • , Akira Ishihama

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

抄録

Laboratory cultures of a single species of bacteria harboring the same genetic background include heterogeneous cell populations, each differing in apparent morphology and physiology, as found in natural environments. To get insights into difference in the genome expression between individual cells, we constructed various types of the cell chip for monitoring the growth and fate of individual bacterial cells. Immobilization of portions of Escherichia coli culture within these cell chips was established after raising the local temperature in the presence of poly-(N-isopropylacrylamide) (PNIPAAm). The newly developed cell-chip system allows the investigation of activity and regulation of green fluorescent protein (GFP)-fused promoter in single live-bacterial cells for prolonged time under controlled culture conditions. Using this single-cell observation system, we succeeded, for the first time, the real-time single-cell assay of promoter activity of the E. coli gcl gene encoding glyoxylate carboligase as a model system, and the kinetics of gcl induction by an effector glyoxylate. Marked heterogeneity was found in the expression level of the gcl promoter. The heterogeneity in gcl promoter activity was, however, confirmed by Flow cytometry of suspension cultures. Our success provides an experimental system for the increased demand of single-cell biology in bacterial studies.

本文言語英語
ページ(範囲)1111-1122
ページ数12
ジャーナルGenes to Cells
巻15
号11
DOI
出版ステータス出版済み - 11月 2010
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 遺伝学
  • 細胞生物学

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