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In situ microscopy for on‐line determination of biomass
Author(s) -
Bittner C.,
Wehnert G.,
Scheper T.
Publication year - 1998
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/(sici)1097-0290(19981005)60:1<24::aid-bit3>3.0.co;2-2
Subject(s) - in situ , line (geometry) , biomass (ecology) , microscopy , environmental science , biochemical engineering , biology , materials science , microbiology and biotechnology , chemistry , engineering , ecology , optics , mathematics , physics , organic chemistry , geometry
A sensor is presented, which allows on‐line microscopic observation of microorganisms during fermentations in bioreactors. This sensor, an In Situ Microscope (ISM) consists of a direct‐light microscope with a measuring chamber, integrated in a 25 mm stainless steel tube, two CCD‐cameras, and two frame‐grabbers. The data obtained are processed by an automatic image analysis system. The ISM is connected with the bioreactor via a standard port, and it is immersed directly in the culture liquid—in our case Saccharomyces cerevisiae in a synthetic medium. The microscopic examination of the liquid is performed in the measuring chamber, which is situated near the front end of the sensor head. The measuring chamber is opened and closed periodically. In the open state, the liquid in the bioreactor flows unrestricted through the chamber. In closing, a defined volume of 2,2 · 10 −8 mL of the liquid becomes enclosed. After a few seconds, when the movement of the cells in the enclosed culture has stopped, they are examined with the microscope. The microscopic images of the cells are registered with the CCD‐cameras and are visualized on a monitor, allowing a direct view of the cell population. After detection, the measuring chamber reopens, and the enclosed liquid is released. The images obtained are evaluated as to cell concentration, cell size, cell volume, biomass, and other relevant parameters simultaneously by automatic image analysis. With a PC (486/33 MHz), image processing takes about 15 s per image. The detection range tested when measuring cells of S. cerevisiae is about 10 6 to 10 9 cells/mL (equivalent to a biomass of 0.01 g/L to 12 g/L). The calculated biomass values correlate very well with those obtained using dry weight analysis. Furthermore, histograms can be calculated, which are comparable to those obtained by flow cytometry. © 1998 John Wiley & Sons, Inc. Biotechnol Bioeng 60: 24–35, 1998.