Genotoxicity monitoring using a 2D-spectroscopic GFP whole cell biosensing system

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Amelita J. Bartolome
  • Roland Ulber
  • Thomas Scheper
  • Eran Sagi
  • Shimshon Belkin

Organisationseinheiten

Externe Organisationen

  • University of Santo Tomas
  • Hebrew University of Jerusalem (HUJI)
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Details

OriginalspracheEnglisch
Seiten (von - bis)27-32
Seitenumfang6
FachzeitschriftSensors and Actuators, B: Chemical
Jahrgang89
Ausgabenummer1-2
PublikationsstatusVeröffentlicht - 21 Jan. 2003

Abstract

A 2D-spectroscopic genotoxicity biosensing system is presented. This optical sensing system monitors the genotoxicant-induced expression of green fluorescent protein (GFP) in a recombinant Escherichia coli strain. In this organism, GFP synthesis is driven by the recA gene promoter of the bacterial SOS DNA repair system. Using nalidixic acid as a model genotoxicant, we have demonstrated a response range that varies as a function of the excitation wavelength. When GFP fluorescence was monitored at 510 nm, the linear working range to nalidixic acid was within the range of 0.03-0.3 ppm at 390 nm excitation and 0.05-0.3 ppm at 480 nm excitation.

ASJC Scopus Sachgebiete

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Genotoxicity monitoring using a 2D-spectroscopic GFP whole cell biosensing system. / Bartolome, Amelita J.; Ulber, Roland; Scheper, Thomas et al.
in: Sensors and Actuators, B: Chemical, Jahrgang 89, Nr. 1-2, 21.01.2003, S. 27-32.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Bartolome AJ, Ulber R, Scheper T, Sagi E, Belkin S. Genotoxicity monitoring using a 2D-spectroscopic GFP whole cell biosensing system. Sensors and Actuators, B: Chemical. 2003 Jan 21;89(1-2):27-32. doi: 10.1016/S0925-4005(02)00423-9
Bartolome, Amelita J. ; Ulber, Roland ; Scheper, Thomas et al. / Genotoxicity monitoring using a 2D-spectroscopic GFP whole cell biosensing system. in: Sensors and Actuators, B: Chemical. 2003 ; Jahrgang 89, Nr. 1-2. S. 27-32.
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title = "Genotoxicity monitoring using a 2D-spectroscopic GFP whole cell biosensing system",
abstract = "A 2D-spectroscopic genotoxicity biosensing system is presented. This optical sensing system monitors the genotoxicant-induced expression of green fluorescent protein (GFP) in a recombinant Escherichia coli strain. In this organism, GFP synthesis is driven by the recA gene promoter of the bacterial SOS DNA repair system. Using nalidixic acid as a model genotoxicant, we have demonstrated a response range that varies as a function of the excitation wavelength. When GFP fluorescence was monitored at 510 nm, the linear working range to nalidixic acid was within the range of 0.03-0.3 ppm at 390 nm excitation and 0.05-0.3 ppm at 480 nm excitation.",
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T1 - Genotoxicity monitoring using a 2D-spectroscopic GFP whole cell biosensing system

AU - Bartolome, Amelita J.

AU - Ulber, Roland

AU - Scheper, Thomas

AU - Sagi, Eran

AU - Belkin, Shimshon

N1 - Funding information: A.J.B. wishes to thank the Deustche Akademischer Austauschdienst (DAAD) for the PhD scholarship grant. This project was supported by a research grant from the Land Niedersachen Min. f. Wissenchaft & Kultur 16.11.1998—25 A.5—76 251-99-2/98 (ZN549) to T.S. and S.B.

PY - 2003/1/21

Y1 - 2003/1/21

N2 - A 2D-spectroscopic genotoxicity biosensing system is presented. This optical sensing system monitors the genotoxicant-induced expression of green fluorescent protein (GFP) in a recombinant Escherichia coli strain. In this organism, GFP synthesis is driven by the recA gene promoter of the bacterial SOS DNA repair system. Using nalidixic acid as a model genotoxicant, we have demonstrated a response range that varies as a function of the excitation wavelength. When GFP fluorescence was monitored at 510 nm, the linear working range to nalidixic acid was within the range of 0.03-0.3 ppm at 390 nm excitation and 0.05-0.3 ppm at 480 nm excitation.

AB - A 2D-spectroscopic genotoxicity biosensing system is presented. This optical sensing system monitors the genotoxicant-induced expression of green fluorescent protein (GFP) in a recombinant Escherichia coli strain. In this organism, GFP synthesis is driven by the recA gene promoter of the bacterial SOS DNA repair system. Using nalidixic acid as a model genotoxicant, we have demonstrated a response range that varies as a function of the excitation wavelength. When GFP fluorescence was monitored at 510 nm, the linear working range to nalidixic acid was within the range of 0.03-0.3 ppm at 390 nm excitation and 0.05-0.3 ppm at 480 nm excitation.

KW - 2D-spectroscopy

KW - Genotoxicity

KW - Green fluorescent protein

KW - Whole cell biosensor

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U2 - 10.1016/S0925-4005(02)00423-9

DO - 10.1016/S0925-4005(02)00423-9

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VL - 89

SP - 27

EP - 32

JO - Sensors and Actuators, B: Chemical

JF - Sensors and Actuators, B: Chemical

SN - 0925-4005

IS - 1-2

ER -

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