Title of article :
Further development of silk sericin as a biomaterial: comparative investigation of the procedures for its isolation from Bombyx mori silk cocoons
Author/Authors :
Chirila, Traian V. Queensland Eye Institute - South Brisbane, Australia , Suzuki, Shuko Queensland Eye Institute - South Brisbane, Australia , McKirdy, Natalie C. Queensland Eye Institute - South Brisbane, Australia
Abstract :
There is significant research dedicated to fibroin
and sericin, the two major proteinaceous components of the
silk threads produced by the domesticated silkworm,
Bombyx mori. While fibroin is accepted as an established
biomaterial, sericin (BMSS) has been largely neglected in
this respect on the account of a hypothetical allergenic
activity. Research over the past decade, including our
previous study (Prog Biomater 2:14, 2013), demonstrated
the biocompatibility of sericin and feasibility of its use as a
biomaterial. However, the current procedures for isolating
BMSS from the raw silk cocoons can only provide
degraded proteins, where the size and distribution of their
molecular masses are significantly altered. Based on the
plausible assumption that such effects can have a negative
impact on the properties of sericin as a biomaterial, in this
study we investigated comparatively four different extraction
procedures in order to find the method that would
cause the least hydrothermal degradation of BMSS. The
products resulting from commonly used procedures (extraction
in boiling water, alkaline extraction, and extraction
in autoclave) were compared to those resulting from
aqueous extraction in mild conditions as described a long
time ago by Anderlini. The molecular mass distribution in
BMSS resulting from each procedure was examined by
electrophoretic analysis performed on sodium dodecyl
sulphate-polyacrylamide gel (SDS-PAGE), while the conformational
changes pertaining to secondary structure of
BMSS were evaluated by Fourier transform infrared-attenuated
total reflectance (FTIR-ATR) spectrometry. The
electrophoretograms indicated that the aqueous extraction
in mild conditions conducted at 50 C for durations up to
4 weeks, with/without stirring, afforded the least degraded
BMSS. The infrared spectrometric analysis showed that
BMSS resulting from the mild extraction method contained
predominantly b-sheet conformations, while the more
degradative methods (alkaline, autoclave) led to BMSS
where the random-coil conformations were preferential.
The long-duration aqueous extraction at 50 C (but not at
60 C) appeared as a valid option for obtaining BMSS
products where the hydrothermally induced fragmentation
of the polypeptidic components is minimized.
Keywords :
Bombyx mori silk , Silk proteins , Sericin , Methods of extraction , Molecular mass distribution
Journal title :
Progress in Biomaterials
Journal title :
Progress in Biomaterials