The stable isotope ratios of C-bonded H (δ2Hn values) can be used to locate soil samples for
forensic purposes
because of their close correlation with the δ2H values
of precipitation. Post-sampling bacterial activity might change the
δ2Hn values via glycolysis. We tested
to which degree C-bonded H is replaced by H from ambient water under
favorable and unfavorable growing conditions. We provided two heterotrophic
bacteria (Bacillus atrophaeus, Escherichia coli) with glucose (favorable) or lysine
(unfavorable) under aerobic conditions. We assessed the H incorporation
from ambient water via 2H labeling. We found that the H
incorporation into bacterial biomass in the glucose treatment was
79 ± 5.9% (B. atrophaeus) and
43 ± 3.0% (E. coli), likely as
a consequence of glycolysis and conservation of the δ2H value in the anabolic mode of the tricarboxylic acid (TCA) cycle.
Differences between species were possibly related with different compositions
of metabolite mixtures. The bacteria did hardly grow with lysine while
respiration continued, and we found no H incorporation because the
catabolic mode of the TCA cycle, which was active when the bacteria
grew on lysine, is associated with CO2 release and a complete
cleavage of former C–2H bonds. Our results support
the glycolysis pathway as a mechanism underlying the incorporation
of ambient-water H into the C-bonded H pool of bacteria. Stressful
conditions forcing bacteria into a catabolism-dominated metabolism
disable the incorporation of ambient-water H, and δ2Hn values can be applied to identify the origin of soil
samples in forensics.