posted on 2017-03-15, 03:05authored byTan Wei Shang
In recent years,
immense interest is placed on the bioactivities of endophytic fungi due to the
possibility of these microorganisms synthesizing pharmacologically active
compounds with vast biotechnological applications. This project aimed to study
the biodiversity and explore the bioactivities of endophytic fungi from a local
medicinal plant Andrographis paniculata (Hempedu Bumi) which is rich with
various ethnobotanical properties. It was hypothesized that endophytic fungi
from this medicinal plant possess potentials as bioactive compound producers.
The biodiversity of endophytic fungi from this plant was successfully
established, with 50 of the isolates clustered into 15 different genera, mainly
Colletotrichum, Guignardia, Fusarium, Phomopsis and Diarporthe. Root tissues
have the highest number of isolates (21 isolates), followed by stem (11
isolates), leaf (15 isolates), and finally flower tissues (3 isolates).
Bioprospecting studies revealed different bioactivities of the endophytes. Four
of the 50 isolates showed antibacterial activity, with one isolate HBR18 (Aspergillus
sclerotiorum) showing broad-spectrum activity against 10 bacterial pathogens
tested. For antioxidant assays, 18 endophytic isolates demonstrated
2.2’-Diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity greater
than 50%. This study is the first to report Guignardia sp. as potential free
radical scavenger (92.27% scavenging rate). Three Colletotrichum sp. isolates
(HBR4, HBR14, HBL8) demonstrated the highest ferric ion reducing potential
(FRP) with FRP value greater than 1.900. Total phenolic content (TPC) of all 50
isolates were between 0.12 – 10.85 mg/mL culture filtrate with no specific
association found between TPC, FRP and DPPH values. Enzymatic screening showed
all 50 isolates were capable of producing at least four of the eight enzymes
screened, with one isolate HBR1 (Corynespora cassiicola) producing seven
enzymes. For antifungal potential, three and seven endophytic isolates
inhibited the growth of Ganoderma boninense and Fusarium oxysporum f. sp.
cubense race4 (FOCR4) up to 50%. G. boninense and FOCR4 are the causal agents
for basal stem rot disease and Fusarium wilt in oil palm and banana
plantations, respectively. Isolate HBR9 (Aspergillus nomius) exhibited
promising inhibitory activities towards both fungal pathogens and hence was
selected for further studies. The growth conditions of isolate HBR9 was
optimized to be 1% sucrose, 1% sodium nitrate in pH 5 Czapek Dox medium
cultured at static condition at room temperature (25± 2 oC). Investigation of
the antifungal mechanisms of isolate HBR9 revealed two groups of antifungal
compounds (heat-sensitive and heat-stable) contributing to its inhibitory
activities. Heat-sensitive metabolites were determined to be potent fungal cell
wall-degrading enzymes, namely β-glucanase and chitinase. These antifungal
enzymes were characterized based on the optimum incubation time, pH stability,
thermos-stability, effect of substrate concentration and kinetic studies.
Heat-stable antifungal metabolites, on the other hand, constituted of various
phytochemicals tested in this study (saponins, phenolic compounds, cardiac
glycosides, steroids, flavonoids, terpenoids, and anthraquinone). Isolate HBR9
was also found to produce hydrolytic enzymes such as amylase, cellulase,
xylanase, and lipase which advantage this isolate to procure nutriment from
host plants while eliciting protective mechanisms against pathogens especially
G. boninense and FOCR4. However, genome analysis of isolate HBR9 revealed
complete aflatoxin-producing gene clusters. Production of aflatoxin, a potent
liver carcinogen, was tested positive in isolate HBR9. Future work should
concentrate on silencing aflatoxin gene expression before further phytochemical
purification and application of the metabolites of HBR9 in the field to avoid
aflatoxin contamination in oil palm and banana crops.