1
Zentrum Angewandte Chemie Institut für Technische Chemie Callinstr. 5 , D-30167 Hannover Andreas Prediger 1 , Tim Höpfner , Patrick Lindner , Mehriban Akin , Merve Yuksel , Sascha Beutel , Suna Timur , Thomas Scheper 1 1 2 2 1 2 1 1 Leibniz University Hannover, , Callinstr. 5, D-30167 Hannover Institute of Technical Chemistry A multifunctional at-line analysis system for monitoring of cell cultivations Control software An integration of further sensors into the system is desired. A fibre optical detection of the pH-value could be carried out analogously to the pO -value detection. The used enzymes in the biosensor could be exchanged to allow the detection of other relevant biological substances such as lactate or organic acids. New image processing algorithms are constantly developed. An aim for the future is the cell viability determination via optical properties of the cell without the need to stain them. One approach for this is the implementation of neuronal networks. A new flow microscope prototype for fluorescence measurements is under development. It will be used for at-line monitoring of micro algae cultivations and could be integrated into the multisensor system as well. 2 Funded by 2 Ege University, Faculty of Science, Biochemistry Department, 35100 Bornova-Izmir, Turkey Perspectives Fig.3: Monitoring of a cultivation S.cerevisiae Image processing Fig.1: Schematic setup of the multisensor system Biosensor Introduction In biotechnology lots of interesting products are produced in suspension cell cultures. Process security and a high quality of the final product are essential in this field. This is why continuous monitoring of the bioprocesses is essential. A multifunctional at-line analysis system was developed to allow the automatic acquisition of process data from different sensor systems. Fig.1 shows a simplified schematic setup of the device. A flow microscope (Fig.2) allows the monitoring of cell density and cell viability. Dead cells are stained using dyes (e.g. Methylen blue) and the acquired images are analyzed with an image processing software. The developement of glucose and ethanol concentrations during a cultivation can be monitored using a dual biosensor. The pO -value is determined via fibreoptical measurements. A mixing chamber that is attached to an injection system allows the automatic dilution of samples and thus the monitoring of broad cell density and concentration ranges. 2 Fig.2: Flow Microscope 1 1 2 3 3 4 5 5 6 1: Connection for control and power supply 2: CCD camera 3: Micrometer screws 4: Microscope body 5: Connections for flow cell 6: Illumination system with connection cable Fig.4: Original image Fig.5: Result image of software The acquired images are analyzed with the processing software " . Using an edge-detection algorithm the cells in the image are detected via grey value gradients. Subsequently the mean grey value of the cell is determined. If it exceeds a defined threshold the cells are marked as living (yellow box). If it is below the threshold the cells are marked as dead (blue circle). Life and Death" Five living cells and one dead cell are detected by the image processing software A flow electrode with a dual biosensor is used for the detection of glucose and ethanol concentrations. Pyranoseoxidase und ethanoloxidase are immobilized separately on two gold electrodes using PAMAM (Polyamidoamine). They catalyze the following reactions: Glucose + O Gluconolactone + H O Ethanol + O Acetaldehyde +HO The substrate concentration is measured indirectly via the oxygen consumption. Oxygen is detected at a potential of -700 mV and thus no interference with media ingredients occurs. The linear range of both biosensors is between 0 and 0.5 mM. A stability test showed that after 11h 98% (Pyranoseoxidase) and 94% (Ethanoloxidase) of the initial enzyme activity were retained. 2 2 2 2 2 2 in the WTZ Programme Published in: Akin . 2011 A new set up for multi-analyte sensing: At-line bio-process monitoring. Biosensors & Bioelectronics 26:4532-4537. et al . Fig. 3 shows the result from monitoring of an example cultivation of with the multisensor system. After calibration all data were acquired completely automatically. S.cerevisiae The device is controlled with the software FIA-Master. Via a RS232 serial interface all pumps, valves and the illumination system can be controlled. All actions are determined with a script that is easily created and modified for different applications.

Zentrum Angewandte Chemie · 2015. 7. 30. · Zentrum Angewandte Chemie Institut für Technische Chemie Callinstr. 5 , D-30167 Hannover Andreas Prediger1, Tim Höpfner , Patrick Lindner

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Page 1: Zentrum Angewandte Chemie · 2015. 7. 30. · Zentrum Angewandte Chemie Institut für Technische Chemie Callinstr. 5 , D-30167 Hannover Andreas Prediger1, Tim Höpfner , Patrick Lindner

Zentrum Angewandte ChemieInstitut für Technische ChemieCallinstr. 5 , D-30167 Hannover

Andreas Prediger1, Tim Höpfner , Patrick Lindner , Mehriban Akin ,

Merve Yuksel , Sascha Beutel , Suna Timur , Thomas Scheper

1 1 2

2 1 2 1

1Leibniz University Hannover, , Callinstr. 5, D-30167 HannoverInstitute of Technical Chemistry

A multifunctional at-line analysis systemfor monitoring of cell cultivations

Control software

An integration of further sensors into the system is desired. A fibre optical detection of thepH-value could be carried out analogously to the pO -value detection. The used enzymes

in the biosensor could be exchanged to allow the detection of other relevant biologicalsubstances such as lactate or organic acids.New image processing algorithms are constantly developed. An aim for the future is thecell viability determination via optical properties of the cell without the need to stain them.One approach for this is the implementation of neuronal networks.A new flow microscope prototype for fluorescence measurements is under development.It will be used for at-line monitoring of micro algae cultivations and could be integrated intothe multisensor system as well.

2

Funded by

2Ege University, Faculty of Science, Biochemistry Department, 35100 Bornova-Izmir, Turkey

Perspectives

Fig.3: Monitoring of a cultivationS.cerevisiae

Image processing

Fig.1: Schematic setup of the multisensor system

Biosensor

IntroductionIn biotechnology lots of interesting products are produced in suspension cellcultures. Process security and a high quality of the final product are essentialin this field. This is why continuous monitoring of the bioprocesses is essential.Amultifunctional at-line analysis system was developed to allow the automaticacquisition of process data from different sensor systems. Fig.1 shows asimplified schematic setup of the device.A flow microscope (Fig.2) allows the monitoring of cell density and cell viability.Dead cells are stained using dyes (e.g. Methylen blue) and the acquiredimages are analyzed with an image processing software. The developementof glucose and ethanol concentrations during a cultivation can be monitoredusing a dual biosensor. The pO -value is determined via fibreoptical

measurements.A mixing chamber that is attached to an injection system allows the automaticdilution of samples and thus the monitoring of broad cell density andconcentration ranges.

2

Fig.2: Flow Microscope1

1

2

3

3

4

5

56

1: Connection for control and power supply2: CCD camera3: Micrometer screws4: Microscope body5: Connections for flow cell6: Illumination system with connection cable

Fig.4: Original image

Fig.5: Result imageof software

The acquired images are analyzedwith the processing software "

.Using an edge-detection algorithmthe cells in the image are detectedvia grey value gradients.Subsequently the mean grey value ofthe cell is determined. If it exceeds adefined threshold the cells aremarked as living (yellow box). If it isbelow the threshold the cells aremarked as dead (blue circle).

Life

and Death"

Five living cells and onedead cell are detected

by the image processingsoftware

Aflow electrode with a dual biosensor is used for the detection of glucose andethanol concentrations.Pyranoseoxidase und ethanoloxidase are immobilized separately on twogold electrodes using PAMAM (Polyamidoamine). They catalyze thefollowing reactions:

Glucose + O Gluconolactone + H O

Ethanol + O Acetaldehyde + H O

The substrate concentration is measured indirectly via the oxygenconsumption. Oxygen is detected at a potential of -700 mV and thus nointerference with media ingredients occurs.The linear range of both biosensors is between 0 and 0.5 mM. A stability testshowed that after 11h 98% (Pyranoseoxidase) and 94% (Ethanoloxidase) ofthe initial enzyme activity were retained.

2 2 2

2 2 2

in the WTZ Programme

Published in: Akin . 2011 A new set up for multi-analyte sensing: At-line bio-process monitoring.Biosensors & Bioelectronics 26:4532-4537.

et al .

Fig. 3 shows the result from monitoring of an example cultivation ofwith the multisensor system. After calibration all data were

acquired completely automatically.S.cerevisiae

The device is controlled with the software FIA-Master. Via a RS232 serialinterface all pumps, valves and the illumination system can be controlled. Allactions are determined with a script that is easily created and modified fordifferent applications.