Characterization of allelopathic algicide produced by solid-state fermentation of okara byproducts
Harmful algae bloom (HAB) has become an increasingly worrisome problem with impact spanning across crucial industries, such as: agriculture, water utilities, recreation, and tourism. Despite the disadvantages of prolonged and indiscriminate use of traditional copper algicides, formulations contai...
Saved in:
Main Author: | |
---|---|
Other Authors: | |
Format: | Thesis-Doctor of Philosophy |
Language: | English |
Published: |
Nanyang Technological University
2025
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/181824 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Summary: | Harmful algae bloom (HAB) has become an increasingly worrisome problem with
impact spanning across crucial industries, such as: agriculture, water utilities, recreation,
and tourism. Despite the disadvantages of prolonged and indiscriminate use of traditional
copper algicides, formulations containing copper has remained as one of the most utilized
algicides on the market, with copper sulphate and chelated copper taking a major market
share. Continual discovery and development of novel algicides which are biodegradable,
operate at a species-specific level, and has limited negative impacts on the targeted
ecosystems is crucial to update the toolbox which water managers use to remove and
inhibit algae growth under specific applications. Among biological methods, direct
bacteria-to-microalgae contact, and bacterial extracellular metabolites are identified as
potential algicidal agents that can fulfil the demand for green and sustainable algicides.
Often, the algicidal metabolites are presented as extracellular metabolites which bacteria,
fungi, protozoans, and plants secrete into their living environment, whether as a direct
reaction to the presence of microalgal competitors or with microalgal inhibition as a
secondary unintended consequence. In Chapter II, the cell-free fermentate produced from the aerobic fermentation of
P. chlororaphis in LB media exhibited a higher algal inhibition rate than those produced
under microaerobic conditions against the tested strains (Chlorella sp. ATCC 14854 and
P. tricornutum UTEX LB642); this result presents a stark contrast against previous
studies. Later, the serendipitous discovery of a bright orange coloration within the
fermentate served as a base hypothesis for the identification of potential algae-inhibiting
metabolites produced by P. chlororaphis. Among the well-known, orange-colored
metabolites of P. chlororaphis, phenazine derivatives (phenazine-1-carboxylic acid, PCA
and phenazine-1-carboxamide, PCN) were hypothesized to be the active algae inhibiting
component. A potential link was established between phenazine derivatives and algal
inhibition rate (%) against Chlorella sp. (ATCC 14854) and P. tricornutum (UTEX
LB642) based on the positive correlation between the concentration of phenazine
derivatives produced as detected by HPLC-DAD analysis, and the incubation time of P. chlororaphis under aerobic condition. Aerobic fermentation produced a maximum
concentration of phenazine derivatives at 26.48 μg/mL on the 72H of aerobic
fermentation which coincided with the maximum algal inhibition rate of 72.25% after
24H incubation with Chorella sp. and suggests a concentration-dependent mode of algal
inhibition. These results provided a theoretical foundation upon which further algicide
discovery work can be built on. Considering the drawbacks of using traditional copper algicides in live
aquaculture and agriculture processes and coupled by key market drivers in the APAC
region where consumers are demanding more sustainable production processes, it is
imperative to discover novel methods to sustainably produce algicides using existing
byproduct and sidestreams generated from Singapore’s agri-food ecosystem. Chapter III
of this thesis explores okara, an agricultural byproduct generated from soymilk
production as a substrate for solid-state fermentation. It was used as the sole nutrient
source in a ‘proof-of-concept’ experiment to sustain the growth of rhizosphere bacterium,
P. chlororaphis and to produce the suspected algicidal extracellular metabolites –
phenazine derivatives and rhamnolipids congeners in a batchwise solid-state fermentation.
Using targeted LC-MS Q-ToF metabolomic analysis, the batch fermentation experiments
found conclusive presence of phenazine-1-carboxylic acid (PCA) and potential presence
of glycolipids though their acid hydrolysate products [C8, C10, C12, C12:1] in fermented
okara extracts (FOE). LC-MS Q-ToF analysis has not found clear evidence of phenazine-
1-carboxamide (PCN) and rhamnolipids congeners in the samples. However, chemical
assays have provided evidence for the presence of a pH-responsive foaming agent as an
unintended response to pH changes when rhamnolipid standards and potentially
rhamnolipids-containing samples were pH-adjusted during the methylene blue
complexation assay. The challenge of using chemical assay to locate phenazine
derivatives and rhamnolipid fractions was the substantial interference from the
nutritiously rich okara substrate since both methods of measuring rhamnolipid content:
anthrone reducing sugar assay, and methylene blue complexation assay have respectively
shown a higher amount of reducing sugar and anionic surfactant ‘rhamnolipids’ in nonfermented
extract as compared to fermented extract. This confuses the authenticity of
‘rhamnolipid’ detected in the fermented samples since the result might have been contributed by the remnants of the non-transformed okara substrate. The confirmed
presence of PCA also does not dismiss the possibility of other compounds acting as
algicides since P. chlororaphis could produce more than just phenazines or rhamnolipids.
Microbial degradation of okara may also contribute algicidal component of a substrate
origin, instead of bacterium origin since okara contains a rich unfractionated trove of
amino acids and peptides which may function as algicides in their own rights. Faced with
ambiguous results, further refinement to experimental designs and the existing hypothesis
would serve as an impetus towards furthering the knowledge of how extracellular
metabolites of P. chlororaphis may serve a more functional role within the food security
and safety ecosystem and find its own niche as a green algicide within the current circular
economy paradigm. |
---|