In microbial communities such as those found in biofilms, individual organi
sms most often display heterogeneous behavior with respect to their metabol
ic activity, growth status, gene expression pattern, etc. In that context,
a novel reporter system for monitoring of cellular growth activity has been
designed. It comprises a transposon cassette carrying fusions between the
growth rate-regulated Escherichia coli rrnBP1 promoter and different varian
t gfp genes. It is shown that the pi promoter is regulated in the same way
in E. coli and Pseudomonas putida, making it useful for monitoring of growt
h activity in organisms outside the group of enteric bacteria. Construction
of fusions to genes encoding unstable Gfp proteins opened up the possibili
ty of the monitoring of rates of rRNA synthesis and, in this way, allowing
on-line determination of the distribution of growth activity in a complex c
ommunity. With the use of these reporter tools, it is demonstrated that ind
ividual cells of a toluene-degrading P. putida strain growing in a benzyl a
lcohol-supplemented biofilm have different levels of growth activity which
develop as the biofilm gets older. Cells that eventually grow very slowly o
r not at all may be stimulated to restart growth if provided with a more ea
sily metabolizable carbon source. Thus, the dynamics of biofilm growth acti
vity has been tracked to the level of individual cells, cell clusters, and
microcolonies.