The ability to monitor changes in metabolites and corresponding
gene transcription within living cells is highly desirable. However,
most current assays for quantification of metabolites or for gene
transcription are destructive, precluding tracking the real-time dynamics
of living cells. Here, we used the intracellular elemental sulfur
in a Thiophaeococcus mangrovi cell
as a proof-of-concept to link the quantity of metabolites and relevant
gene transcription in living cells by a nondestructive Raman approach.
Raman spectroscopy was utilized to quantify intracellular elemental
sulfur noninvasively, and a computational mRR (mRNA and Raman) model
was developed to infer the transcription of genes relevant to elemental
sulfur. The results showed a significant linear correlation between
the exponentially transformed Raman spectral intensity of intracellular
elemental sulfur and the mRNA levels of genes encoding sulfur globule
proteins in T. mangrovi. The mRR model
was verified independently in two genera of Thiocapsa and Thiorhodococcus, and the mRNA levels predicted
by mRR showed high consistency with actual gene expression detected
by real-time polymerase chain reaction (PCR). This approach could
enable noninvasive assessment of the quantity of metabolites and link
the pertinent gene expression profiles in living cells, providing
useful baseline data to spectroscopically map various omics in real
time.