Encapsulation of host-derived probiotics using functional polysaccharides
Probiotics can be used to address the challenge of infectious diseases in aquaculture. However, they are vulnerable to acidic gastric conditions, thereby reducing their cell viability. To solve this issue, microencapsulation is commonly used to protect probiotics from the harsh environments of...
Saved in:
Main Author: | |
---|---|
Other Authors: | |
Format: | Final Year Project |
Language: | English |
Published: |
Nanyang Technological University
2023
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/166642 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Summary: | Probiotics can be used to address the challenge of infectious diseases in aquaculture.
However, they are vulnerable to acidic gastric conditions, thereby reducing their cell
viability. To solve this issue, microencapsulation is commonly used to protect
probiotics from the harsh environments of the stomach. It is worth noticing that the
functional properties of encapsulants are often overlooked in previous studies.
Therefore, this project aims to evaluate the functionality of common encapsulants,
exemplified by using polysaccharides, and fabricate a probiotic encapsulation system
using selected polysaccharides that work synergistically with Enterococcus hirae, the
host-derived probiotic, for Jade Perch. Needle extrusion was employed to encapsulate
the bacteria with alginate and Kappa-Carrageenan (KC), with alginate being the
“golden standard” for probiotic encapsulation and KC being selected based on its Short
Chain Fatty Acids (SCFAs) production and the change in the gut bacteria composition
after co-incubation. SCFAs serve as an energy source and promote the growth of fish,
hence a higher concentration of SCFAs is more favourable. KC was found to be able
to suppress the growth of an opportunistic pathogen Edwardsielle. Regarding the
encapsulation process, various parameters, such as the polysaccharides concentration,
the flow rate, and the temperature of the salt solution, were optimized for the ionic
gelation process. The study found that 2% alginate and KC were the most suitable
concentrations as they provide a good balance in the protectability and release ability.
A flow rate of 1 mL/min was used as it allows the proper formation and hardening of
particles. Higher flow rates resulted in extremely small particles being formed whereas
lower flow rates resulted in the formation of big lumps of particles. Besides that, an
ice bath must be employed during the extrusion of KC particles as KC is a thermal sensitive gel, where cooling temperature can facilitate in maintaining the shape of the
particles. Furthermore, encapsulated probiotics exhibited higher cell viability than
unencapsulated ones upon exposure to Simulated Gastro Fluid (SGF). For instance,
encapsulation using polysaccharides improve the cell viability around 10^6 CFU/mL.
Additionally, Scanning Electron Microscope (SEM) imaging at 2000× magnification
confirmed the presence of spherical shape E.hirae probiotics embedded in the extruded
alginate and KC microparticles, which were approximately 1-2 µm. In the future, in
vivo feeding trials will be conducted for Jade Perch to evaluate the persistence of the
delivered bacteria in the gut, pathogen resistance, and other performances of
encapsulated probiotics, to achieve the manipulation of the host gut microbiota and
increase disease resistance. |
---|