Sea Slug Mixes Ingredients in
Chemical Defense Before Firing at Predators
Antimicrobial property of secretion
has potential industrial applications
When threatened by predators, sea slugs defend themselves
by ejecting a potent inky secretion into the water
consisting of hydrogen peroxide, ammonia and several
types of acids. A team of CBN researchers has found
that this secretion is produced from normally inert
chemicals stored separately in two glands. The discovery,
published in the Dec. 15 on-line edition of the Journal
of Experimental Biology, provides insight into
a natural chemical process with potential industrial
applications.
In the study, Georgia State University biologist
Charles Derby, PhD, and his colleagues examined the
ink and opaline glands of Aplysia sea slugs
for the chemicals L-lysine, L-arginine and an enzyme
protein called escapin. In previous research, Derby’s
team determined that escapin mediates the chemical
reaction with L-lysine and L-arginine that results
in the defensive secretion. Using a variety of chemical
and molecular techniques, the scientists identified
L-lysine and L-arginine in the opaline gland, which
produces the sticky white component of the secretion,
and escapin in the ink gland, which produces the
purple dye in the secretion.
“Aplysia packages these innocuous
precursors separately and then releases them simultaneously
into its mantle cavity at the precise time when they
are needed,” explained Derby. “This mechanism
insures the secretion’s potency against attacking
predators to enable sea slugs to escape.”
Aplysia employs a variety of mechanisms
to defend against predators. Its secretion stimulates
feeding behaviors in spiny lobsters, but deters these
behaviors in other animals. In previous studies,
Derby and his team also identified an antimicrobial
property in the secretion resulting from the chemical
reaction between escapin and L-lysine. The scientists
are currently examining the chemical process that
results in the antimicrobial component and also are
attempting to identify Aplysia predators
which are affected by this property of the secretion.
“The antimicrobial property probably evolved
to work against predators,” said Derby. “But
it might also function as an antimicrobial salve
for Aplysia’s own wounds.”
Derby’s team, who discovered escapin and holds
a provisional patent for its genetic sequence, has
been studying the protein for its potential applications
as an antimicrobial compound for the healthcare and
marine industries. The team has determined that escapin
prevents the growth of all major forms of bacteria
as well as other microbes.
“As we learn more about how escapin works
in Aplysia, we will hopefully be able to
reproduce its chemical properties in the laboratory,” said
Derby.
In addition to Derby, co-authors of the Journal
of Experimental Biology study are Paul Johnson,
PhD, Cynthia Kicklighter, PhD, Manfred Schmidt,
PhD, Michiya Kamio, PhD, Hsiuchin Yang, PhD, and
Phang Tai, PhD, of the Georgia State biology department.
Other co-authors include physiologists Dimitry
Elkin and William Michel, PhD, of the University
of Utah School of Medicine.
Derby’s research is supported by grants from
the National Science Foundation, National Institutes
of Health and the Georgia Research Alliance.
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