Randers-Eichhorn L, Albano C R, Sipior J, Bentley W E, Rao G
Department of Chemical and Biochemical Engineering, University of Maryland Baltimore County, Baltimore, Maryland 21250, USA.
Biotechnol Bioeng. 1997 Sep 20;55(6):921-6. doi: 10.1002/(SICI)1097-0290(19970920)55:6<921::AID-BIT9>3.0.CO;2-I.
We present an intensity based sensor designed for on-line monitoring of green fluorescent protein, a revolutionary marker of protein expression. The device consisted of a blue light emitting diode as the excitation source. A band pass excitation filter cut off light longer than 490 nm. The light was directed into a bifurcated optical fiber bundle with the common end inserted into a stainless steel housing equipped with a quartz window. The fiber bundle and stainless steel housing are steam sterilizable. The emission radiation was collected through a long wave pass filter to reject the excitation light shorter than 505 nm and was detected by a photomultiplier tube. The signal was amplified and sent to a computer for recording time course data. The sensor was tested in an Escherichia coli fermentation of JM105 transformed with pBAD-GFP. The on-line signal was compared to off-line fluorescence spectrophotometer measurements. The on-line profile closely followed the off-line. Western blot data showed that with a time shift, the sensor was able to both continuously and quantitatively monitor expression of green fluorescent protein on-line in real time.
我们展示了一种基于强度的传感器,该传感器设计用于在线监测绿色荧光蛋白(一种蛋白质表达的革命性标记物)。该装置由一个蓝色发光二极管作为激发源。一个带通激发滤光片截止波长大于490nm的光。光被导入一个分叉的光纤束,其公共端插入一个配备石英窗的不锈钢外壳中。光纤束和不锈钢外壳可进行蒸汽灭菌。发射辐射通过一个长波通滤光片收集,以滤除波长小于505nm的激发光,并由一个光电倍增管进行检测。信号被放大并发送到计算机以记录时间进程数据。该传感器在转化了pBAD-GFP的JM105大肠杆菌发酵过程中进行了测试。将在线信号与离线荧光分光光度计测量结果进行了比较。在线曲线与离线曲线紧密吻合。蛋白质印迹数据表明,经过时间偏移后,该传感器能够实时、连续且定量地在线监测绿色荧光蛋白的表达。