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SUMMARY:Recombinant Expression of Silk Sericin in Duckweed (Lemna japonica
 ) as a Sustainable Platform for Functional Biomaterial Production
DTSTART;VALUE=DATE-TIME:20261002T070000Z
DTEND;VALUE=DATE-TIME:20261002T071500Z
DTSTAMP;VALUE=DATE-TIME:20260915T154449Z
UID:indico-contribution-445-2937@cern.ch
DESCRIPTION:Speakers: Julia Eva Fortmueller (Weizmann Institute of Science
  )\nSilk sericin\, a glycoprotein produced by Bombyx mori\, naturally coat
 s and binds silk fibroin fibers during cocoon formation. Beyond this role\
 , sericin's biocompatibility\, low immunogenicity\, and bioactive properti
 es\, including antioxidant and adhesive effects\, have made it attractive 
 for a range of biomedical and biomaterial applications. However\, conventi
 onal degumming methods are harsh\, reduce protein purity\, and are constra
 ined by low yield and poor reproducibility between batches.\nTo overcome t
 hese limitations\, we explored duckweed (Lemna japonica)\, a fast-growing\
 , readily transformable aquatic plant\, as an alternative production platf
 orm. We generated stable transgenic duckweed lines expressing silk sericin
 \, representing one of the first efforts to establish duckweed as a platfo
 rm for recombinant silk-derived protein expression\, and characterized exp
 ression levels and tissue-specific accumulation. Soluble sericin was recov
 ered from plant extracts via heat-treatment method.\nWe then evaluated the
  functional bioactivity of duckweed-derived sericin using an established m
 ammalian cell model\, benchmarking its performance against commercially av
 ailable sericin under standardized conditions. Quantitative and morphologi
 cal assessments confirmed that duckweed-derived sericin significantly enha
 nced the assessed functional endpoints\, outperforming commercial sericin.
 \nThis work establishes proof-of-concept for duckweed as a scalable\, plan
 t-based platform for producing functional recombinant sericin via a mild e
 xtraction route\, offering a sustainable\, cost-effective alternative to c
 onventional methods with broader implications for recombinant protein prod
 uction in plants and downstream biomaterial applications.\n\nhttps://indic
 o.unina.it/event/117/contributions/2937/
LOCATION:Department of Agricultural Sciences of the University of Napoli F
 ederico II\, Portici\, Italy Sala Cinese
URL:https://indico.unina.it/event/117/contributions/2937/
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BEGIN:VEVENT
SUMMARY:Towards a subunit oral vaccine to Newcastle disease in transgenic 
 duckweeds
DTSTART;VALUE=DATE-TIME:20261002T064500Z
DTEND;VALUE=DATE-TIME:20261002T070000Z
DTSTAMP;VALUE=DATE-TIME:20260915T154449Z
UID:indico-contribution-445-2936@cern.ch
DESCRIPTION:Speakers: Ron Vunsh (Weizmann Institute for Sciences)\nNewcast
 le virus disease (ND) in poultry is highly contagious. Weak strains cause 
 loss in egg production\, virulent strains kill the birds1. NDV virions pos
 ses an envelop and contain a single molecule of linear\, negative sense RN
 A coding for at least six proteins. The important proteins for subunit vac
 cines are two glycoproteins: the hemagglutinin-neuraminidase (HN)\, and th
 e fusion protein (F)\, which are used as antigens for immunization. Immuni
 zation is currently by injection\, nasal spray\, ocular or drinking water 
 that contain the HN antigen. \n\nDuckweeds are small\, edible monocot plan
 ts that float on the surface of fresh water and need only light\, air and 
 some common minerals for rapid growth. Plants of these genera are preferre
 d food as indicated by their name. Transgenic edible plants can deliver va
 ccines to different animals2.\n\nWe introduced HN and the F protein genes 
 into a duckweed species to deliver these antigens for induction of protect
 ive immune response in chickens. We get high expression of both antigens i
 n the transgenic plants\, which grow normally with no apparent phenotypic 
 change.\n\nhttps://indico.unina.it/event/117/contributions/2936/
LOCATION:Department of Agricultural Sciences of the University of Napoli F
 ederico II\, Portici\, Italy Sala Cinese
URL:https://indico.unina.it/event/117/contributions/2936/
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BEGIN:VEVENT
SUMMARY:Duckweed as a platform for oral vaccines in sustainable fish aquac
 ulture
DTSTART;VALUE=DATE-TIME:20261002T063000Z
DTEND;VALUE=DATE-TIME:20261002T064500Z
DTSTAMP;VALUE=DATE-TIME:20260915T154449Z
UID:indico-contribution-445-2935@cern.ch
DESCRIPTION:Speakers: Olena Kishchenko (Leibniz Institute of Plant Genetic
 s and Crop Plant Research (IPK) Germany\; Institute of Cell Biology and Ge
 netic Engineering\, National Academy of Science of Ukraine)\nVaccination i
 s a cornerstone of modern health management. It`s particular important in 
 intensive animal production systems\, such as aquaculture\, where high sto
 cking densities facilitate the rapid spread of pathogens. Oral vaccines of
 fer a stress-free\, scalable alternative to traditional fish injections. O
 ur study explores duckweed as platform for vaccine production and as vehic
 le for oral administration. Using a deconstructed potato virus X-based tra
 nsient expression system [1]\, recombinant proteins analogs of antigens of
  koi herpesvirus (KHV) and carp edema virus (CEV) were expressed in duckwe
 ed. Freeze-drying was shown to preserve the recombinant antigens in the du
 ckweed biomass\, enabling long-term storage at room temperature. Obtained 
 freeze-drying duckweed biomass expressing KHV antigens was used for carp i
 mmunization via intraperitoneal injection and intubation [2]. Both methods
  of administration induced release of the specific KHV-neutralising antibo
 dies. Such data provide a strong support for the efficacy of duckweed as p
 roducer of oral vaccines. Transient expression of recombinant proteins in 
 duckweed can facilitate and accelerate the development of oral vaccines fo
 r animals.\n\nhttps://indico.unina.it/event/117/contributions/2935/
LOCATION:Department of Agricultural Sciences of the University of Napoli F
 ederico II\, Portici\, Italy Sala Cinese
URL:https://indico.unina.it/event/117/contributions/2935/
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