Systematic analysis of a Monoterpene synthase from bangun-bangun (Plectranthus amboinicus lour. spreng)
Plectranthus amboinicus (Lour.) Spreng, is an aromatic medicinal herb noted for its therapeutic and nutritional properties attributed by the presence of terpenoids. To date, molecular research on terpenoids biosynthesis from this herb is still limited and the terpene synthases responsible for ter...
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| Format: | Thesis |
| Language: | English |
| Published: |
2021
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| Subjects: | |
| Online Access: | http://psasir.upm.edu.my/id/eprint/92670/1/FBSB%202021%2014%20-%20IR.pdf |
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| Summary: | Plectranthus amboinicus (Lour.) Spreng, is an aromatic medicinal herb noted for
its therapeutic and nutritional properties attributed by the presence of terpenoids.
To date, molecular research on terpenoids biosynthesis from this herb is still
limited and the terpene synthases responsible for terpenoids production in P.
amboinicus have yet to be described. Terpenoids have high demands in their
applications as flavours and fragrances in food and cosmetics, and also as
therapeutic agents in pharmaceutical products. Unfortunately, nature rarely
produces these compounds in abundance. Hence, isolating the desired gene
from the P. amboinicus for production of the terpenoid compounds in a suitable
heterologous system poses an alternative way to overcome such limitations in
the natural sources. The aim of this study was to isolate and characterise the P.
amboinicus terpene synthase. Among the approaches involved are profiling of
volatiles that contributed to the distinctive aroma of P. amboinicus conducted
using GC-MS, accompanied by characterisation of the recombinant terpene
synthase and terpenoids production in an Escherichia coli system, gene
expression analysis in planta using quantitative real-time PCR and in silico
structure prediction using homology modelling and protein docking. Volatiles
profiling of P. amboinicus leaves revealed the presence of 46 % monoterpenes
and 53 % sesquiterpenes comprising of α-bergamotene, carvacrol,
caryophyllene, ρ-cymene, γ-terpinene and terpene alcohols. A putative
monoterpene synthase coding sequences (designated as PamTps1) with an
open reading frame of 1797 bp encoding a predicted protein of 598 amino acids
with more than 60 % identity to known terpene synthases of Lamiaceae was
isolated. A soluble recombinant PamTps1 with estimated size of ~79 kDa was
successfully expressed via pET-32b(+) expression vector in Escherichia coli
Rosetta™ 2(DE3) system at 28 °C with 0.5 mM IPTG induction. Enzyme
characterisation revealed that the PamTps1 catalysed the conversion of geranyl
pyrophosphate (GPP, C10) and farnesyl pyrophosphate (FPP, C15) into linalool
and nerolidol, respectively. Biochemical properties of PamTps1 exhibited the highest activity at an optimal pH and temperature of 6.5 and 30 °C, respectively,
in the presence of 20 mM magnesium as a cofactor. The Michaelis-Menten
constant (Km) and catalytic efficiency (kcat /Km) were 16.72 ± 1.32 μM and 9.57 x
10-3 μM-1 s-1, respectively showed that the PamTps1 had a higher binding affinity
and specificity for GPP instead of FPP as expected for a monoterpene synthase.
The recombinant E. coli harbouring PamTps1 produced 13.6 ± 0.2 μg/ml and
10.6 ± 0.1 μg/ml linalool and nerolidol after 72 h and 24 h incubation,
respectively. These outcomes validated the multi-substrate use of this enzyme
in producing linalool and nerolidol, both in the in vivo and in vitro systems.
Transcript expression analysis revealed that PamTps1 was up-regulated in
leaves (42-fold of expression level) instead of stems which were associated with
linalool emission following a diurnal rhythm regulated by circadian clock of the
plant. Homology modelling of PamTps1 was predicted using BPPS (1N24) with
67 % sequence identity as a template. PamTps1 active site pocket analysis
revealed nine aromatic residues (W268, Y272, Y299, F371, Y378, Y379, F447,
Y517, and Y523) that defined the hydrophobic walls of the active site cavity and
shaped the active site for proper substrate binding and folding. While residues
from the RRx8W motif, RxR motif, H-α1, and J-K loops formed the active site lid,
protecting the highly reactive carbocationic intermediates from solvents. The
dual-substrates used by PamTps1 were hypothesised due to the architecture
and residues lining the catalytic site that can accommodate larger substrate
(FPP) as demonstrated by protein modelling and docking analysis. The
PamTps1 herein was identified as a linalool/nerolidol synthase, and this is the
first study describing isolation and characterisation of such substrate promiscuity
terpene synthase from the P. amboinicus. This study provides an initial insight
into terpenoids biosynthesis in this herb that can be exploited for production of
these natural products using metabolic engineering in both microbial and plant
systems. |
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