The potential of pyrolysis mass spectrometry to distinguish closely related
cyanobacterial strains was assessed by using the technique to compare symb
iotic cyanobacteria isolated from the hornwort Phaeoceros laevis and free-l
iving cyanobacterial strains at the same field site. The same strains had p
reviously been compared using polymerase chain reaction-based DNA fingerpri
nting techniques (West & Adams 1997, Appl. Environ. Microbiol. 63: 4479-448
4). Many of the strains were grouped identically by the two techniques, alt
hough there were some differences, possibly resulting from the ability of t
hese cyanobacteria to develop a range of specialised cell types having diff
erent chemical compositions to the vegetative cells. Although growth condit
ions were chosen to suppress cellular differentiation, this may not always
have been completely successful. With careful control of growth conditions
pyrolysis mass spectrometry has considerable potential as an additional too
l for the phenetic comparison of cyanobacterial strains. It has the advanta
ge that analysis is directly derived from whole cells, and hence is simpler
and cheaper than DNA-based methods, although it does require the growth of
axenic strains. The technique may be particularly useful in the study of s
ome of the more cryptic unicellular and non-heterocystous filamentous cyano
bacterial groups, in which the lack of cellular differentiation should mini
mise any variability in the chemical composition of cells.