The potential of focussed beam reflectance measurement (FBRM) as a tool to monitor changes in biomass concentration was investigated in a number of biological systems. The measurement technique was applied to two morphologically dissimilar plant cell suspension cultures, Morinda citrifolia and Centaurea calcitrapa, to a filamentous bacteria, Streptomyces natalensis, to high density cultures of Escherichia coli and to a murine Sp2/0 hybridoma suspension cell line, 3-2.19. In all cases, the biomass concentration proved to be correlated with total FBRM counts. The nature of the correlation varied between systems and was influenced by the concentration, nature, size and morphology of the particle under investigation.

A morphological interpretation is presented for data collected during growth of a filamentous organism, using a focused beam reflectance measurement (FBRM) system. The morphology of the organism was also obtained using conventional semiautomatic image analysis to support the interpretation of the FBRM data. The model organism employed is the filamentous soil-borne actinomycete Streptomyces natalensis, which produces the antifungal agent pimaricin. The organism was cultivated both in shake flasks and in a bench-scale stirred tank bioreactor. It was found that FBRM could be used to track changes in the morphology of the organism throughout the course of its growth on both scales. These changes were highlighted using both the median chord length and length-weighted mean chord length obtained from the chord length distribution measured with the FBRM probe. The ability of the FBRM probe to respond to changes in both the size and morphology of mycelial aggregates was supported by standard image analysis parameters, including equivalent diameter, convex area, and compactness.

In this paper the use of a focused beam reflectance measurement (FBRM) particle characterisation probe was investigated as a tool for monitoring the growth of the filamentous bacteria Streptomyces natalensis. The optimum operating parameters of the probe were identified, and it was found that the sample agitation rate had the largest effect on the mean value of a number of statistics of the chord length distribution (CLD) measured by the FBRM probe. A series of fractions of the particle size distribution was generated by sieving. It was found that the mean chord length measured by the probe responded to changes in the size distribution examined, increasing from 57.2 µm to 69.9 µm with an increase in the upper particle size from 180 µm to 300 µm. It was also found that the average total counts measured by the probe also increased with increasing sample concentration. This relationship was further investigated and it was found that in the normal range of biomass levels experienced in a fermentation (up to 4.0 g dm −3 ) there was an apparently linear relationship between counts and concentration. However, as concentration was increased further the relationship became increasingly non-linear.

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