Abstract:
Moringa oleifera Lam. is one of the world’s most useful medicinal plants. Different parts
of the M. oleifera tree contain a rich profile of important minerals, proteins, vitamins, and various
important bioactive compounds. However, there are differences in the phytochemical composition of
the medicinal plant’s raw materials due to seasonal variation, cultivation practices, and post-harvest
processing. The main objective of this study was therefore to determine the effect of harvesting
frequencies on selected bioactive compounds of a M. oleifera cultivar (PKM1) grown in a hydroponic
system under a shade net structure. Three harvesting frequency treatments were applied in the study,
with the plants harvested at every 30 days (high frequency), 60 days (intermediate frequency), and
90 days (low frequency) respectively. 1H-NMR was used for data acquisition, and multivariate data
analysis by means of principal component analysis (PCA), partial least square discriminatory analysis
(PLS-DA), and orthogonal partial least square discriminatory analysis (OPLS-DA) were applied
to determine the changes in the leaf metabolite profile, and also to identify the spectral features
contributing to the separation of samples. Targeted metabolite analysis was used to match the NMR
peaks of the compounds with the NMR chemical shifts of the contribution plot. The contribution
plot showed that the increase in concentration of some compounds in aliphatic, sugar and aromatic
regions contributed to the separation of the samples. The results revealed that intermediate and
low harvesting frequencies resulted in a change in the leaf metabolite profile. Compounds such as
chlorogenic acid, ferulic acid, vanillic acid, wogonin, esculetin, niazirin, and gamma-aminobutyric
acid (GABA) showed an increase under intermediate and low harvesting frequencies. These results
provide insight into the effect of harvesting frequencies on the metabolite profile and associated
medicinal activity of M. oleifera.
Description:
SUPPLEMENTARY MATERIAL: FIGURE S1: Contribution plot showing metabolite peaks in the NMR aliphatic, sugar and aromatic regions of M. oleifera leaf metabolomics associated with March sample separation under high harvesting frequency as shown in Figure 2, FIGURE S2: OPLS-DA loading score plot showing 1H-NMR spectral data of M. oleifera (cultivar PKM1) metabolite profile under low/ intermediate and high harvesting frequency, FIGURE S3: PLSDA score plot showing 1H-NMR spectral data of M. oleifera (cultivar PKM1) metabolite profile under low/intermediate and high harvesting frequencies, showing separation between day 0 and end point harvesting, FIGURE S4: PLS-DA model validity permutation test for M. oleifera (cultivar PKM1) metabolite profile under low, intermediate and high harvesting frequencies, TABLE S1: 1H-NMR spectral regions of annotated compounds that contributed to the separation of leave samples.
