Aims: Conjugated hydroxycinnamates, such as chlorogenic acid (caffeoyl-quin
ic acid), are widely consumed in a Western diet, coffee being one of the ri
chest sources. Ingested hydroxycinnamate esters can reach the large intesti
ne essentially unaltered, and may then be hydrolysed by esterases produced
by the indigenous microflora. This study is aimed at identifying bacterial
species responsible for the release of natural antioxidants, such as hydrox
ycinnamic acids, in the human large intestine.
Methods and Results: Thirty-five isolates recovered after anaerobic batch c
ulture incubation of human faecal bacteria in a chlorogenic acid-based medi
um were screened for cinnamoyl esterase activity. Six isolates released the
hydroxycinnamate, ferulic acid, from its ethyl ester in a plate-screening
assay, and these were identified through genotypic characterization (16S rR
NA sequencing) as Escherichia coli (three isolates), Bifidobacterium lactis
and Lactobacillus gasseri (two strains). Chlorogenic acid hydrolysing acti
vities were essentially intracellular. These cinnamoyl esterase-producing o
rganisms were devoid of other phenolic-degrading activities.
Conclusions: The results show that certain gut bacteria, including some alr
eady recognized as potentially health-promoting (i.e. species belonging to
the genera Bifidobacterium and Lactobacillus), are involved in the release
of bioactive hydroxycinnamic acids in the human colon.
Significance and Impact of the Study: Free hydroxycinnamates, including caf
feic, ferulic and p-coumaric acids, exhibit antioxidant and anticarcinogeni
c properties both in vitro and in animal models. Given that the gut flora h
as a major role in human nutrition and health, some of the beneficial effec
ts of phenolic acids may be ascribed to the microflora involved in metaboli
sm.