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Article

Phenolics and Flavonoids Compounds, Phenylanine Ammonia Lyase and Antioxidant Activity Responses to Elevated CO2 in Labisia pumila (Myrisinaceae)

by
Hawa Z.E. Jaafar
*,
Mohd Hafiz Ibrahim
and
Ehsan Karimi
Department of Crop Science, Faculty of Agriculture, University Putra Malaysia, Serdang 43400, Selangor, Malaysia
*
Author to whom correspondence should be addressed.
Molecules 2012, 17(6), 6331-6347; https://doi.org/10.3390/molecules17066331
Submission received: 22 March 2012 / Revised: 17 May 2012 / Accepted: 21 May 2012 / Published: 25 May 2012
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Abstract

:
A split plot 3 × 3 experiment was designed to examine the impact of three concentrations of CO2 (400, 800 and 1,200 µmol·mol−1) on the phenolic and flavonoid compound profiles, phenylalanine ammonia lyase (PAL) and antioxidant activity in three varieties of Labisia pumila Benth. (var. alata, pumila and lanceolata) after 15 weeks of exposure. HPLC analysis revealed a strong influence of increased CO2 concentration on the modification of phenolic and flavonoid profiles, whose intensity depended on the interaction between CO2 levels and L. pumila varieties. Gallic acid and quercetin were the most abundant phenolics and flavonoids commonly present in all the varieties. With elevated CO2 (1,200 µmol·mol−1) exposure, gallic acid increased tremendously, especially in var. alata and pumila (101–111%), whilst a large quercetin increase was noted in var. lanceolata (260%), followed closely by alata (201%). Kaempferol, although detected under ambient CO2 conditions, was undetected in all varieties after exposure. Instead, caffeic acid was enhanced tremendously in var. alata (338~1,100%) and pumila (298~433%). Meanwhile, pyragallol and rutin were only seen in var. alata (810 µg·g−1 DW) and pumila (25 µg·g−1 DW), respectively, under ambient conditions; but the former compound went undetected in all varieties while rutin continued to increase by 262% after CO2 enrichment. Interestingly, naringenin that was present in all varieties under ambient conditions went undetected under enrichment, except for var. pumila where it was enhanced by 1,100%. PAL activity, DPPH and FRAP also increased with increasing CO2 levels implying the possible improvement of health-promoting quality of Malaysian L. pumila under high CO2 enrichment conditions.

1. Introduction

Carbon dioxide is regarded as one of the most limiting factors in photosynthesis. Currently, the CO2 concentration in ambient atmosphere is about 380 µmol·mol−1 and it is expected to increase by 600 µmol·mol−1 CO2 by end of 2050 [1]. The prospect of improving photosynthesis in crops through CO2 enrichment has interested plant scientists for many years [2]. Enriching plants with high levels of CO2 has been proven to increase plant growth, morphology, development, and yield of many crops, and this response is a function of CO2 rate and duration of exposure [3]. Crops under enriched CO2 atmosphere acquire positive features with enhanced plant adaptation and growth. The greatest advantages of CO2 enrichment is in the enhancement of leaf gas exchange capacity, particularly under undesirable climatic conditions [4].
Plant antioxidants have been a focus of attention in recent years due to the health preservation functions of these components that can help reduce the threat of chronic diseases such as cancer, diabetes and hypertension. This is attributed to the high scavenging activity of antioxidants towards free radicals that are usually associated with these diseases [5]. It is currently known that phenolic acids and flavonoids are antioxidants with high anti-inflammatory and anti-carcinogenic activities [6,7]. It is also known that phenolics and flavonoids can function as reducing agents, free radical scavengers and quenchers of singlet oxygen formation [8]. High contents of natural flavonoids and phenolic acids are found in green tea, fruits, and vegetables, while some amounts of phenolics also exist in red wine and coffee [9]. These components of polyphenols have been proven to have significant roles in the curing cancer and other human ailments [10]. The concentration of phenolics and flavonoids in plants varies among organs, tissues and developmental stage, and is influenced by environmental factors such as temperature, UV and visible radiation, nutrient and water availabilities, and atmospheric CO2 concentration [11].
The exposure of medicinal plants to high level of CO2 may give positive response in the form of increased anti-oxidative properties [12]. Furthermore, several researchers have found increase in anti-oxidative activity under elevated CO2 exposure due to increases in the levels of some secondary metabolite compounds that might up-regulate the antioxidant activity [13,14]. As it is generally known that secondary metabolism and primary metabolism are inter-related by the rates at which substrates are diverted from primary pathways and channeled into the secondary biosynthetic routes [15]. Several environmental factors affecting growth, photosynthesis and other parts of primary metabolism will also affect secondary metabolism [16]. Resource allocation hypotheses such as the carbon-nutrient balance (CNB) [17] and growth differentiation balance (GDB) [18] have been proposed by researchers to predict the effects of increased CO2 concentration on plant secondary metabolites. They assume that changes in carbon source-sink relationship, as a consequence of carbon availability, determines variations in the relative partitioning of carbon to growth and production of carbon based secondary metabolites (CBSM). Recently, in Malaysia, it has been found that the enrichment of Labisia pumila and Zingiber officinale with high levels of CO2 could increase the secondary metabolite production [19,20]. The same result was in agreement with data previously obtained from Pinus taeda [4], Podophyllum hexandrum [21], Digitalis lanata [22], Brassica oleracea [23] and Hypericum perforatum [24].
Labisia pumila, Benth. popularly known as Kacip Fatimah, is a sub-herbaceous plant with creeping stems from the family Myrsinaceae that is found widespread in Indochina and throughout the Malaysian forest. Recently, it was found that this herb is a good source of natural antioxidants due to its high content of anthocyanins, flavonoids, and phenolic acids [25,26]. Results of elevated CO2 imposition on total phenolics and flavonoids have been reported by Ibrahim et al. [27], however, there is no available information on the effects of CO2 concentration on the profiling of phenolics and flavonoids composition and antioxidant activity of this plant under high CO2 conditions, especially for three recognized varieties of this plant (var alata, pumila and lanceolata). Previous research has shown that there no significant differences in the total phenolics, flavonoids and carbohydrate content between those varieties [28]. This study was performed to evaluate the effects of elevated CO2 enrichment on leaf of phenolics and flavonoids compounds in the three varieties of L. pumila. The DPPH, FRAP activity and phenylalanine ammonia lyase (PAL) were also determined in the study.

2. Results and Discussion

2.1. HPLC Analysis of Phenolics

In the study, initially, four phenolics compounds were determined, i.e., (gallic acid, pyragallol, caffeic acid and salicylic acid). However, only three phenolics compounds were revealed to be present as no salicylic acid was detected in all three varieties under ambient levels or exposure to elevated CO2 conditions.
Leaf profiling results for phenolic compounds were observed to be significantly influenced by the interaction between CO2 and varieties (p ≤ 0.01; Table 1; Figure 1). Among the phenolic acid compounds profiled, gallic acid exhibited the highest concentration. With increasing CO2 the gallic acid levels increased tremendously, but at different rates for the different varieties under different CO2 concentrations. Increased CO2 levels from 400 to 800 µmol·mol−1 CO2, saw the gallic acid component in var. alata improve by 86% (448 µg·g−1 dry weight vs. 837 µg·g−1 dry weight) followed by var. pumila (30%) and lanceolata (16.4%) (Table 2). However further exposure to 1,200 µmol·mol−1 CO2 showed a remarkable improvement of gallic acid in var. lanceolata (130%), more than var. alata (111%) and var. pumila (101%), implying that increased CO2 levels had a direct impact on gallic acid concentration that varied among varieties. Under exposure to elevated CO2 (1,200 µmol·mol−1) the gallic acid content of var. alata and lanceolata was higher than pomegranate (901 µg·g−1 dry weight), but lower than onion that recorded 1,490 µg·g−1 dry weight. The present data indicate that enrichment of L. pumila with high CO2 can possibly enhance the production of gallic acid in the three varieties.
Table
Table 1. Phenolics content (µg·g−1 dry weight) in three varieties of Labisia pumila grown under different CO2 concentration.
Table 1. Phenolics content (µg·g−1 dry weight) in three varieties of Labisia pumila grown under different CO2 concentration.
CO2 levels (µmol·mol−1)VarietiesGallic acid *PyragallolCaffeic acid
Alata448.12 ± 2.44 d810.03 ± 2.4447.83 ± 3.22 f
400Pumila215.48 ± 4.32 gND43.92 ± 2.11 f
Lanceolata406.03 ± 3.22 fND115.21 ± 1.14 e
Alata837.434 ± 0.87 bND215.51 ± 2.54 c
800Pumila282.17 ± 0.43 gND177.35 ± 2.56 d
Lanceolata474.33 ± 3.67 cNDND
Alata948.28 ± 6.77 aND543.88 ± 3.44 a
1200Pumila435.69 ± 9.87 eND237.86 ± 5.66 b
Lanceolata935.91 ± 4.34 aNDND
ND = not detected. All analyses are the mean of nine measurements ± standard error of mean. Results expressed in µg·g−1of dry plant material. Means not sharing a common letter were significantly different at p ≤ 0.05.*
Molecules 17 06331 g001 550
Figure 1. The RP-HPLC chromatogram of phenolics compounds in the leaves of Labisia pumila. Identification of compounds: gallic acid, pyrogallol and caffeic acid.
Figure 1. The RP-HPLC chromatogram of phenolics compounds in the leaves of Labisia pumila. Identification of compounds: gallic acid, pyrogallol and caffeic acid.
Molecules 17 06331 g001
Table
Table 2. Percent of increase or decrease of phenolics compounds in three varieties of Labisia pumila grown under elevated CO2 concentration (800 and 1,200 µmol·mol−1).
Table 2. Percent of increase or decrease of phenolics compounds in three varieties of Labisia pumila grown under elevated CO2 concentration (800 and 1,200 µmol·mol−1).
Phenolic compoundsVar. alataVar. pumilaVar. lanceolata
800 (µmol·mol−1)1,200 (µmol·mol−1)800 (µmol·mol−1)1,200 (µmol·mol−1)800 (µmol·mol−1)1,200 (µmol·mol−1)
Gallic acid+86%+111%+30%+101%+16.4%+130%
Pyragallol−100%−100%0%0%0%0%
Caffeic acid+338%+1010%+298%+433%−100%−100%
Results expressed in percent; + and − indicate respectively increase and decrease of component concentrations when exposed to CO2.
What was more interesting with modification of CO2 is the non-detectability of pyragallol in var. alata when exposed to 800 and 1,200 µmol·mol−1 CO2 although the component were only detected in var. alata at high concentration under ambient CO2 condition. A similar effect was observed with var. lanceolata where caffeic acid was not detected when the plant exposed to elevated CO2 (800 and 1,200 µmol·mol−1 CO2), although a significant increase in caffeic acid concentration was observed in both var. alata and pumila. The caffeic acid concentration recorded increases by 338% and 1010% for var. alata and 298% and 433% for var. pumila at 800 and 1,200 µmol·mol−1 CO2 respectively. A similar result was obtained by Lindroth et al. [29] whereby exposure to 650 µmol·mol−1 CO2 had increased phenolic compounds (gallic acid, phenolic glycosides, gallotannin, and ellagitannin) in aspen, oak and maple seedlings. Vurro et al. [30] also saw increased phenolics components in Thymus vulgaris with exposure to 500 µmol·mol−1 CO2. They also found supplementation with elevated CO2 increased the superoxide dismutase and gluthatione reductase activity and essential content in the plants. The current results exhibited an enhanced of the medicinal properties of L. pumila, particularly the gallic acid compounds through CO2 enrichment. The increase in phenolics compounds in the current study under elevated CO2 might be attributed to increased L. pumila growth under CO2 exposure that enhanced the concentration of phenolics per gram dry mass basis of L. pumila [31]. The current result showed an agreement with CNB and GDB hypotheses [17,18] that predict an increase in phenolics content under elevated CO2 conditions. From previous study by Ibrahim and Jaafar [27] it was found that the total phenolics and flavonoids have a significant positive correlation with total biomass and specific leaf leaf area that indicated the increase in secondary metabolites content in L. pumila was due to enhanced plant morphology that might contain more plant secondary metabolites [19].

2.2. HPLC Analysis of Flavonoids

The results obtained from the analysis of flavonoids are shown in Table 3. Five flavonoid compounds were analyzed, i.e., rutin, naringenin, myrecetin, quercetin and kaempferol (Figure 2). From the result, it observed that the production of kaempferol became undetectable in the three L. pumila varieties when the plants were exposed to elevated CO2. Under ambient CO2 conditions kaempferol content was found to be higher in var. pumila (221.91 µg·g−1 dry weight), followed by var. alata (186.71 µg·g−1 dry weight) and the least in var. lanceolata, that recorded only 163.71 µg·g−1 dry weight (Table 3). Meanwhile, increasing the CO2 concentration from 400 to 1,200 µmol·mol−1 generally resulted in enhanced quercetin in all of the varieties. Under ambient CO2 levels the quercetin in var. pumila recorded the highest value at 105.66 µg·g−1 dry weight compared to var. alata and var. pumila that recorded 57.61 µg·g−1 dry weight and 56.90 µg·g−1 dry weight, respectively. With increasing CO2 concentration from 800 to 1,200 µmol·mol−1, the increase in quercetin concentration in var, alata (absolute) was by 3-fold (179%) and 4-fold (221%), var. lanceolata by about two and five fold (81%–260%); and lowest increases in quercetin occurred in var. pumila that recorded at only 10%–20% (Table 4). In the present study, elevated CO2 exposure did not enhance quercetin content as much in black tea and papaya that recorded 1,107 and 1,260 µg·g−1 dry weight values, respectively.
Table
Table 3. The concentrations of flavonoid compounds in three varieties of Labisia pumila grown under different CO2 concentration.
Table 3. The concentrations of flavonoid compounds in three varieties of Labisia pumila grown under different CO2 concentration.
CO2 levels (µmol·mol−1)VarietiesFlavonoid content (µg·g−1 dry weight)
KaempferolQuercetin *MyricetinRutinNaringenin
Alata186.71 ± 0.34 b57.61 ± 1.22 g87.81 ± 0.34 cND139.20 ± 2.56 c
400Pumila221.91 ± 0.21 a105.66 ± 2.11 f30.41 ± 2.33 e24.51 ± 0.45 c80.44 ± 0.98 d
Lanceolata162.71 ± 0.31 c56.90 ± 2.34 g27.45 ± 3.11 fND87.11 ± 1.78 e
AlataND160.88 ± 3.44 c273.84 ± 7.44 bNDND
800PumilaND117.42 ± 4.11 eND41.8 ± 3.22 b619.59 ± 9.78 b
LanceolataND103.13 ± 2.78 f49.73 ± 0.54 dNDND
AlataND183.32 ± 5.43 b287.77 ± 0.21 aNDND
1200PumilaND127.52 ± 0.45 dND87.45 ± 2.54 a947.85 ± 9.76 a
LanceolataND205.91 ± 0.21 a85.76 ± 1.45 cNDND
ND = not detected. All analyses are the mean of nine measurements ± standard error of mean. Results expressed in µg·g−1 of dry plant material. Means not sharing a common letter were significantly different at * p ≤ 0.05.
Molecules 17 06331 g002 550
Figure 2. The RP-HPLC chromatogram of flavonoids compounds in the leaves of Labisia pumila. Compound identification as labeled.
Figure 2. The RP-HPLC chromatogram of flavonoids compounds in the leaves of Labisia pumila. Compound identification as labeled.
Molecules 17 06331 g002
Table
Table 4. Percent of increase or decrease of flavonoid compounds in three varieties of Labisia pumila grown under elevated CO2 concentration (800 and 1,200 µmol·mol−1)
Table 4. Percent of increase or decrease of flavonoid compounds in three varieties of Labisia pumila grown under elevated CO2 concentration (800 and 1,200 µmol·mol−1)
Flavonoid compoundsVar alataVar pumilaVar lanceolata
800 (µmol·mol−1)1,200 (µmol·mol−1)800 (µmol·mol−1)1,200 (µmol·mol−1)800 (µmol·mol−1)1,200 (µmol·mol−1)
Kaempferol−100%−100%−100%−100%−100%−100%
Quercetin+179%+221%+10%+20%+81%+260%
Myricetin+210%+226%−100%−100%+75%+203%
Rutin0%0%+70%+262%0%0%
Naringenin−100%−100%+683%+1100%−100%−100%
Results expressed in percent; + and − indicate respectively increase and decrease of component concentrations when exposed to CO2.
The enhancement of myricetin concentration in CO2-enriched L.pumila was only observed in var. alata and var. lanceolata. Under 800 and 1,200 µmol·mol−1 CO2 enrichment myricetin in var. alata increased by 210% and 226%, respectively, compared to ambient conditions that just recorded 87.11 µg·g−1 dry weight (Table 3). In var. lanceolata myricetin concentration improved from 27.45 µg·g−1 dry weight in 400 µmol·mol−1 CO2 to 49.73 µg·g−1 dry weight in 800 µmol·mol−1 CO2 and 85.76 µg·g−1 dry weight under 1,200 µmol·mol−1 CO2 enrichment. Interestingly, myricetin disappeared in var. pumila when it was exposed to higher than ambient CO2. In contrast, the production of rutin and naringinin was only enhanced in var. pumila exposed to higher CO2 of 800 and 1,200 µmol·mol−1 CO2. There were no related increases found in the varieties alata and lanceolata with increasing CO2 level (Table 3). Under ambient conditions, rutin was only detected in var. pumila. As CO2 levels increased from 800 to 1,200 µmol·mol−1 CO2 rutin was enhanced by 70% and 260%, respectively in var. pumila. Meanwhile under ambient CO2 levels the naringenin content was highest in var. alata, recording values of 139.21 µg·g−1 dry weight, followed by var. lanceolata (87.11 µg·g−1 dry weight) and the lowest in var. pumila (80.44 µg·g−1 dry weight). Upon CO2 enrichment with 800 µmol·mol−1 CO2 and 1,200 µmol·mol−1 CO2 the naringenin content in var. pumila increased tremendously by 345% and 581%, respectively, compared to var. alata under ambient conditions. The naringenin content in var. pumila with a value of 947.85 µg·g−1 dry weight under 1,200 µmol·mol−1 CO2 was slightly low compared to grapefruit (1,150 µg·g−1 dry weight), that was found to contain the highest naringenin compared to other plant sources, but is relatively higher compared to tomato (448 µg·g−1 dry weight) and orange (887 µg·g−1 dry weight) [32,33]. Naringenin is a flavonoid that is considered to have a bioactive effect on human health as an antioxidant, free radical scavenger, anti-inflammatory, carbohydrate metabolism promoter, and immune system modulator [20]. The increase in quercetin and naringenin in the present study under elevated CO2 have also been documented by Ghasemzadeh et al. [20] in ginger where they observed increased quercetin and naringenin to be about 26% and 480%, respectively, in ginger leaves when exposed to 800 µmol·mol−1 CO2.
The increase in production of total phenolics and flavonoids in the present study might be due to increased production of total non structural carbohydrates when plants are exposed to elevated CO2. The same observation was also reported by Wang et al. [34] and Malikov et al. [35] in Fragaria ananassa and Betula pendula, respectively, when exposed to high CO2 levels. Ibrahim et al. [19] previously have indicated that the increased production of secondary metabolites in L. pumila under elevated CO2 was due to an accumulation of starch and soluble sugars under high exposure to CO2 (800 and 1,200 µmol·mol−1). In other study, Ibrahim and Jaafar [36] also found that the increase in the production of total phenolics and flavonoids was concomitantly followed by an increase in the production of fructose. The increase in production of secondary metabolites by the increase in fructose content had been observed by Hilal et al. [37] in quinoa seedlings where the increase in total phenolics and flavonoids of the seedlings under UV-B radiation was significantly related to an increase in fructose content in quinoa leaves. The up-regulation of plant secondary metabolites with increasing fructose levels under elevated CO2 might be due to enhanced activity of the pentose phosphate pathway to supply high levels of erythose-4-phosphate, which is used as a substrate for the synthesis of lignin and secondary metabolite compounds in the shikimic acid pathway [38]. The increase in the production of erythose-4-phoshate implies a high production of fructose because both these compounds are synthesized in the same reaction in the pentose phosphate pathway catalyzed by transaldolase [39]. The current results suggest that the increased production of secondary metabolites in L. pumila under elevated CO2 might be due to enhanced production of erythose-4-phosphate under this condition.
Wang et al. [34], obtained the same result when CO2 was enriched at 950 µmol·mol−1 in strawberry the concentrations of flavonoid compounds such as p-coumaroylglucose, dihydroflavonol, quercetin 3-glucoside, quercetin 3-glucuronide, kaempferol 3-glucoside contents, cyanidin 3-glucoside, pelargonidin 3-glucoside, and pelargonidin 3-glucoside succinate were significantly enhanced. The same finding was also observed with Chabot et al. [40] who showed the ability of elevated CO2 concentrations to enhance flavonoid components in Gigaspora margarita where the exposure to high CO2 enhanced flavonoid compounds like quercetin, morin, hesperetin, genistein and chrysin. Estiarte et al. [41] also found exposure that exposure of Triticum aestivum c.v. Yecora Rojo to elevated CO2 at 550 µmol·mol−1 enhanced the production of flavonoids and their components. They observed that a flavonoid compound (isoorientin) content was enhanced by 14% under elevated CO2 conditions. The interspecific difference in the phenolics and flavonoid compounds in this study might be due to the differences in enyzme stimulation for each compound, precursor availability, differing biosynthetic pathways, genetic and carbon allocation to plant parts either for storage or structural components.
Stimulation of secondary metabolite production of L. pumila under elevated CO2 in the present study might be due to increased availability of carbon uptake due to enhancement of leaf gas exchange properties [27]. Under elevated CO2 net photosynthesis was up-regulated, the increase in net photosynthesis with high levels of CO2 increased the production of total non-structural carbohydrates. The increase in production of total non-structural carbohydrate under elevated CO2 was observed in Citrus aurantrium when exposed to 670 µmol·mol−1 CO2 [42]. Plant polyphenols (flavonoid and phenolics) are biosynthesized via several routes and thus constitute a heterogeneous group from the metabolic point of view. The two basic pathways involved are the shikimic acid and the malonic acid pathways. The shikimic acid pathway is able to convert simple carbohydrate precursors derived from glycolysis and pentose phosphate pathway into aromatic amino acids [20]. Previous studies have shown that the increase in phenolic and flavonoid compound is related to the balance between carbohydrate sources and sinks, such that greater source or sink ratio under exposure to elevated CO2 will results in higher phenolic concentration and compounds [43,44]. The present result suggest that enhancement of leaf gas exchange under elevated (photosynthesis) have increase the availability of carbohydrate that enhance the production of phenolics and flavonoid content in L. pumila.

2.3. Phenylalanine Ammonia Lyase (PAL) Activity

The PAL activity was influenced by CO2 concentrations (p ≤ 0.05; Figure 3). In all the three varieties PAL activity was found to be consistently highest under 1,200 µmol−1·mol−1 CO2 with values ranging between (11.24–12.45 nM transcinnamic mg−1 protein hour−1) than at 800 µmol−1·mol−1 CO2 that recorded PAL activity just 6.78 to 7.56 nM transcinnamic mg−1 protein hour−1. Under ambient CO2 conditions, PAL activity in the three varieties registered the lowest values, between 2.94 and 3.87 nM transcinnamic mg−1protein hour−1. The present study showed that as CO2 levels increased, the production of PAL activity was also enhanced. It can be hypothesized that the increase in production of secondary metabolites in the present work could be attributed to an increase in PAL activities under high CO2 levels. This is basically due to the fact that PAL is a precursor to total phenolics and flavonoids biosynthesis [45,46]. The increase in PAL activity in the current study might also be related to reduction in nitrogen content in plant exposed to high CO2 levels which could have increased the availability of phenylalanine (phe) due to restriction in the protein production that enhanced phenylalanine partitioning to the production of CBSM [47]. The increase in PAL activity was usually followed by increase in C/N ratio due to enhanced growth rate under elevated CO2 that easily reduced nitrogen content. Winger et al. [48] indicated that increases in the C/N ratio in plants were an indication of increases in the synthesis of plant secondary metabolites, especially phenolics and flavonoids. The increase in PAL activity under high CO2 was also observed by Matros et al. [49] and Hartley et al. [50] in tobacco and Spergula avensis, respectively.
Molecules 17 06331 g003 550
Figure 3. The effects of different CO2 concentration on PAL activity of three varieties of L. pumila. N = 9. Bars represent standard error of differences between means (SEM).
Figure 3. The effects of different CO2 concentration on PAL activity of three varieties of L. pumila. N = 9. Bars represent standard error of differences between means (SEM).
Molecules 17 06331 g003

2.4. Radical Scavenging Activity (DPPH)

Generally, the highest DPPH antioxidant activity was recorded with 1,200 µmol·mol−1 CO2 followed by 800 µmol·mol−1 CO2 and the lowest for 400 µmol·mol−1 CO2 treatment. The treatment effects of DPPH were contributed by CO2 levels (p ≤ 0.05; Figure 4). At 370 µg/mL, the DPPH antioxidant activity recorded the highest inhibition value (62.89–66.74%) when exposed to 1,200 µmol·mol−1CO2, followed by the 800 µmol·mol−1 CO2 (56.21–59.24%), and the least in the 400 µmol·mol−1 CO2 treatment (44.62–49.52%). This study showed that L. pumila methanolic extract has a good free radical scavenging activity, and, hence, it can be used as a radical scavenging agent acting possibly as a primary antioxidant. This result also implies that exposure to high CO2 concentrations could significantly enhance the DPPH radical scavenging activity of a medicinal plant. It is noteworthy that the DPPH assay principally measures the activity of water-soluble antioxidants [51]. Results of the current work suggest that high CO2 supply is advantageous to L. pumila in the improvement of the antioxidant activity of water-soluble antioxidants. In our previous study, besides phenolics and flavonoid compounds, other water-soluble antioxidants of the extracts such as ascorbic acid and anthocyanin could also exert an additive effect on DPPH radical scavenging activity.
Molecules 17 06331 g004 550
Figure 4. Leaf DPPH scavenging activities in different varieties of L. pumila under different CO2 levels. BHT and α-tocopherol were used as positive controls.
Figure 4. Leaf DPPH scavenging activities in different varieties of L. pumila under different CO2 levels. BHT and α-tocopherol were used as positive controls.
Molecules 17 06331 g004

2.5. Reducing Ability (FRAP)

The ferric reducing antioxidant potential (FRAP) was influenced by CO2 exposure (p ≤ 0.01). The FRAP assay is very simple, fast and precise, and was recently developed to measure the total antioxidant power of biological fluids [52]. The FRAP activity was found to followed similar trend with DPPH antioxidant activity where the highest activity was observed in 1,200 µmol·mol−1 CO2, followed by 800 µmol·mol−1 CO2 and 400 µmol·mol−1 CO2 (Figure 5). The reducing ability of extracts from different varieties of L. pumila with 1,200 µmol·mol−1 CO2 was in the range of 817.14 to 874.26 µm of Fe(II) dry weight, whilst at 800 µmol·mol−1 CO2 the improvement was only 700.27 to 777.24 µm Fe(II) dry weight. Comparatively, at ambient CO2 concentration of 400 µmol·mol−1 CO2 a low reducing ability of the leaf extract (516.33 to 570.12 µm of Fe(II) dry weight; Table 5) was observed. The FRAP values for the methanolic extracts of the leaves, were statistically and significantly lower than vitamin C and α-tocopherol, but higher than that of BHT. Our finding is in agreement with that of Wang et al. [34], who reported the increase in FRAP activity in strawberry fruit by 24% as exposed to elevated CO2 concentrations at 950 µmol·mol−1CO2.The enhancement of DPPH and FRAP activity under elevated CO2 in the present study might be due to increase in production of total phenolics and flavonoids under high levels of CO2. The present study suggest that the increase antioxidant capabilities under elevated CO2 might be to up-regulation of production of plant secondary metabolites that were characterized high production of phenolics and flavonoids compounds.
Molecules 17 06331 g005 550
Figure 5. Leaf total antioxidant activity (FRAP) in different varieties of L. pumila under different CO2 levels. BHT and α-tocopherol were used as positive controls.
Figure 5. Leaf total antioxidant activity (FRAP) in different varieties of L. pumila under different CO2 levels. BHT and α-tocopherol were used as positive controls.
Molecules 17 06331 g005

3. Experimental

3.1. Experimental Location, Plant Materials and CO2 Treatments

The experiment was carried out under a growth house at Field 2, Faculty of Agriculture Glasshouse Complex, Universiti Putra Malaysia (longitude 101°44'N and latitude 2°58'S, 68 m above sea level) with a mean atmospheric pressure of 1.013 kPa. Three-month old L. pumila seedlings that were propagated from leaf cuttings of var. alata, var. pumila and var. lanceolata were left for a month in a nursery to acclimatize until they were ready for the treatments. The seedlings were planted in soil-less medium containing coco-peat, burnt paddy husk and well composted chicken manure in 5:5:1 (v/v) ratio in 25-cm diameter polyethylene bags. Organic fertilizer was applied every two weeks using well composted chicken manure at 20 g/plant. Carbon dioxide enrichment treatment started when the seedlings reached four months of age where plants were exposed to 400, 800 and 1,200 µmol·mol−1 CO2. This 2-factorial experiment was arranged in a split plot using a randomized complete block design with CO2 levels being the main plot, and varieties as the sub-plot replicated three times. Each treatment consisted of nine seedlings. The seedlings were raised in specially constructed growth houses receiving 12-h photoperiod and average photosynthetic photon flux density of 300 µmol·m−2s−1. Day and night temperatures were recorded at 30 ± 1.0 °C and 20 ± 1.5 °C, respectively, and relative humidity at about 70% to 80%. Vapor pressure deficit ranged from 1.01 to 2.52 kPa. Carbon dioxide at 99.8% purity was supplied from a high-pressure CO2 cylinder and injected through a pressure regulator into fully sealed 2 m × 3 m growth houses at 2-h daily and applied continuous from 08:00 to 10:00 a.m. The CO2 distributed inside the growth house by having two opening at the edge of the constructed growth chamber that were mounted a small fan. During enrichment, small low r.p.m. fans were simultaneously used to disperse CO2 evenly inside the constructed growth house. The CO2 concentration at different treatments was measured using Air Sense™ CO2 sensors designated to each chamber during CO2 exposition period. Plants were watered three to four times a day at 5 min per session to ensure normal growth of plant using drip irrigation with emitter capacity of 2 L·h−1. The experiment lasted for 15 weeks from the onset of treatment [53,54].

3.2. Preparation of Extracts for RP-HPLC

Samples were extracted using methanol as a solvent as described by Crozier et al. [55]. Two grams of freeze-dried leaf were weighed and placed into a 100 mL conical flask, and treated with 80% (v/v) aqueous methanol (40 mL). It was followed by an addition of 6 M HCl (10 mL). The mixture was refluxed for 2 h at 90 °C and filtered using Whatman No. 1 filter paper (Whatman, Durham, UK) followed by evaporation of the filtrate using a vacuum rotary evaporator (Buchi, Arbon, Switzerland). The crude extracts were re-dissolved in methanol for RP-HPLC analyses.

3.3. Analyses of Phenolic and Flavonoid Compounds by RP-HPLC

The phenolic and flavonoid compounds of the leaf of Labisa pumila were quantitatively measured by reversed-phase HPLC based on the method described by Crozier et al. [55] with some modifications. Phenolic standards used were gallic acid, caffeic acid and pyrogallol. Flavonoid standards were quercetin, rutin, myricetin, kaempferol and naringin at stock concentrations of 100 µg/mL. An aliquot of sample extract was loaded on the HPLC equipped with an Intersil ODS-3 (5 μm 4.6 × 150 mm, Gl Science Inc) analytical column. Solvents comprising deionised water (solvent A) and acetonitrile (solvent B) were used. The pH of water was adjusted to 2.5 with trifluoroacetic acid. The phenolic and isoflavonoid compounds were detected at 280 nm while flavonoid compounds at 350 nm. The column was equilibrated by 85% solvent A and 15% solvent B. Then the ratio of solvent A was increased to 85% in 50 min followed by reducing solvent B to 15% in 55 min. This ratio was maintained to 60 min for the next analysis with flow rate at 0.6 mL/min.

3.4. Phenylalanine-Ammonia-Lyase (PAL)

Phenylalanine-ammonia-lyase (PAL) activity was measured using the method described by Martinez and Lafuente [56]. The enzyme activity was determined by measuring spectrophotometrically the production of trans-cinnamic acid from L-phenylalanine. Enzyme extract (10 µL) was incubated at 40 °C with 12.1 mM L-phenylalanine (90 µL, Sigma, Chicago, IL, USA) that were prepared in 50 mM Tris-HCl, (pH 8.5). After 15 min of reaction, trans-cinnamic acid yield was estimated by measuring increase in the absorbance at 290 nm. Standard curve was prepared by using a trans-cinnamic acid standard (Sigma) and the PAL activity was expressed as nM trans-cinnamic acid µg−1 protein h−1.

3.5. DPPH Radical Scavenging Assay

The DPPH free radical scavenging activity of each sample was determined according to the method described by Ibrahim et al. [57]. A solution of 0.1 mM DPPH in methanol was prepared. The initial absorbance of the DPPH in methanol was measured at 515 nm. An aliquot (40 µL) of an extract was added to 3 mL of methanolic DPPH solution. The change in absorbance at 515 nm was measured after 30 min. The antiradical activity (AA) was determined using the following formula:
Molecules 17 06331 i001
The optic density of the samples, the control and the empty samples were measured in comparison with methanol. One synthetic antioxidant, BHT (butylated hydroxytoluene) and α-tocopherol, were used as positive controls. The antioxidant capacity based on the DPPH free radical scavenging ability of the extract was expressed in percent of free radical inhibition

3.6. Reducing Ability (FRAP Assay)

The ability to reduce ferric ions was measured using modifying methods of Benzie and Strain [52]. An aliquot (200 µL) of the extract with appropriate dilution was added to FRAP reagent (3 mL, 10 parts of 300 mM sodium acetate buffer at pH 3.6, 1 part of 10 mM TPTZ solution and 1 part of 20 mM FeCl3·6H2O solution) and the reaction mixture was incubated in a water bath at 37 °C. The increase in absorbance at 593 nm was measured after 30 min. The antioxidant capacity based on the ability to reduce ferric ions of the extract was expressed as expressed in µM Fe(II)/g dry mass and compared with those of standards for BHT, ascorbic acid, and α-tocopherol.

3.7. Statistical Analysis

Data were analyzed using analysis of variance by SAS version 17. Mean separation test between treatments was performed using Duncan multiple range test and standard error of differences between means was calculated with the assumption that data were normally distributed and equally replicated [58,59].

4. Conclusions

The manipulation of CO2 may be an effective method to increase the expression of phenolic and flavonoid compounds in L. pumila. The phenolic and flavonoid profiles are dependent on the interspecific variability between CO2 levels and L. pumila varieties. High performance liquid chromatography (HPLC) results showed that gallic acid and quercetin were the most abundant phenolic and flavonoid acids in Malaysian L. pumila varieties, which can be further improved with elevated CO2. From the study, it was noted that the increase in the production of phenolics and flavonoids under elevated CO2 might be due to enhanced PAL activity as CO2 levels increased. From the study, it was observed that the increase in production of plant secondary metabolites in L. pumila was followed by enhancement of the antioxidant activity (DPPH and FRAP) under exposure of elevated CO2. The present results showed the potential use of CO2 enrichment techniques for enhancement of medicinal properties of this plant for future cultivation.

Acknowledgements

The authors are grateful to the Ministry of Higher Education Malaysia and Research Management Centre, Universiti Putra Malaysia for financing this work under the Research University Grant Scheme No. 91007; and the Ministry of Agriculture and Agro-Based Industry for partially funding the work under the Science Fund Scheme No. 5450487.

References and Notes

  1. Taylor, J.A.; Llyold, J. Sources and sinks of atmospheric CO2. Aust. J. Bot. 1992, 40, 401–418. [Google Scholar]
  2. Porter, M.A.; Grodzinski, B. CO2 enrichment of protected crops. Hort. Res. 1985, 7, 345–398. [Google Scholar]
  3. Brevoort, P. The blooming United State botanical market: A new overview. Herbalgram 1998, 44, 33–46. [Google Scholar]
  4. Mark, S.J.; Jackson, S.B. Growth responses of Quercus petraea, Fraxinus excelsior and Pinus sylvestris to elevated carbon dioxide, ozone and water supply. New Phytol. 2000, 146, 437–451. [Google Scholar] [CrossRef]
  5. Byers, T.; Guerrero, N. Epidemilogic evidence for vitamin C and vitamin E in cancer prevention. Am. J. Clin. Nutr. 1995, 62, 1385–1392. [Google Scholar]
  6. Heijnen, C.G.; Haenen, G.R.; Vanacker, F.A.; Vijgh, W.J.; Bast, A. Flavonoids as peroxynitrite scavengers:the role of the hydroxyl groups. Toxicol. In Vitro 2001, 15, 3–6. [Google Scholar] [CrossRef]
  7. Chun, O.K.; Kim, D.O.; Lee, C.Y. Superoxide radical scavenging activity of the major polyphenols in fresh plums. J. Agric. Food Chem. 2003, 51, 8067–8072. [Google Scholar] [CrossRef]
  8. Chan, E.W.C.; Lim, Y.Y.; Wong, L.F.; Lianto, F.S.; Wong, S.K.; Lim, K.K.; Joe, C.E.; Lim, T.Y. Antioxidant and tyrosinase inhibition properties of leaves and rhizomes of ginger species. Food Chem. 2008, 109, 477–483. [Google Scholar] [CrossRef]
  9. Ho, C.T.; Lee, C.Y.; Hungan, M.T. Phenolics compounds in food and their effects on health (analysis, occurance, and chemistry). J. Am. Chem. Soc. 1992, 43, 2–19. [Google Scholar]
  10. Harborne, J.B.; Williams, C.A. Advances in flavonoid research science. Phytochemistry 2000, 55, 481–504. [Google Scholar] [CrossRef]
  11. Booker, F.L. Influence of carbon dioxide enrichment, ozone and nitrogen fertilization on cotton (Gossypium hirsutum L.) leaf and root composition. Plant Cell Environ. 2000, 23, 573–583. [Google Scholar] [CrossRef]
  12. Polle, A.; Eiblmeier, M.; Sheppard, L.; Murray, M. Responses of antioxidative enzymes to elevated CO2 in leaves of beech (Fagus sylatica L.) seedlings grown under a range of nutrient regimes. Plant Cell Environ. 1997, 20, 1317–1321. [Google Scholar]
  13. Schwanz, P.; Polle, A. Antioxidative systems, pigment and protein contents in leaves of adult Mediterranean oak species (Quercus pubescens and Quercus. ilex) with lifetime exposure to elevated CO2. New Phytol. 1998, 140, 411–423. [Google Scholar] [CrossRef]
  14. Pérez-López, U.; Robredo, A.; Lacuesta, M.; Sgherri, C.; Muñoz-Rueda, A.; Navari-Izzo, F.; Mena-Petite, A. The oxidative stress caused by salinity in two barley cultivars is mitigated by elevated CO2. Physiol. Plantarum 2009, 135, 29–42. [Google Scholar] [CrossRef]
  15. Mattson, W.J.; Julkunen-Tiitto, R.; Herms, D.A. CO2 enrichment and carbon partitioning to phenolics: Do plant responses accord better with the protein competition or the growth-differentiation balance models? Oikos 2005, 111, 337–347. [Google Scholar]
  16. Bryant, J.P.; Chapin, F.S.; Klein, D.R. Carbon nutrient balance of boreal plants in relation to vertebrate herbivory. Oikos 1983, 40, 357–368. [Google Scholar] [CrossRef]
  17. Herms, D.A.; Matson, W.J. The dilemma of plants: To grow or defend. Quart. Rev. Biol. 1992, 67, 283–335. [Google Scholar]
  18. Ibrahim, M.H.; Jaafar, H.Z.E.; Rahmat, A.; Abdul Rahman, Z. The relationship between phenolics and flavonoids production with total non structural carbohydrate and photosynthetic rate in Labisia pumila Benth. under high CO2 and nitrogen fertilization. Molecules 2011, 16, 162–174. [Google Scholar]
  19. Ibrahim, M.H.; Hawa, Z.E.J. Carbon dioxide fertilization enhanced antioxidant compounds in Malaysian Kacip Fatimah (Labisia pumila Blume). Molecules 2011, 16, 6068–6081. [Google Scholar] [CrossRef]
  20. Ghasemzadeh, A.; Jaafar, H.Z.; Rahmat, A. Elevated carbon dioxide increases contents of flavonoids and phenolic compounds, and antioxidant activities in Malaysian young ginger (Zingiber officinale Roscoe.) varieties. Molecules 2010, 15, 7907–7922. [Google Scholar] [CrossRef]
  21. Chaturvedi, A.K.; Vashistha, R.J.; Rawat, N. Effect of CO2 Enrichment on photosynthetic behavior of Podophyllum Hexandrum Royle, an endangered medicinal herb. J. Am. Sci. 2009, 5, 113–118. [Google Scholar]
  22. Stuhlfauth, T.; Fock, H.P. Effect of whole season CO2 enrichment on the cultivation of a medicinal plant, Digitalis lanata. J. Agron. Crop Sci. 1990, 164, 168–173. [Google Scholar] [CrossRef]
  23. Schonhof, I.; Klaring, H.P.; Krumbein, A.; Schreiner, M. Interaction between atmospheric CO2 and glucosinolates in broccoli. J. Chem. Ecol. 2007, 33, 105–114. [Google Scholar]
  24. Save, R. Effects of atmospheric carbon dioxide fertilization on biomass and secondary metabolites of some plant species with pharmacological interest under greenhouse conditions. Afinidad 2007, 64, 237–241. [Google Scholar]
  25. Ibrahim, M.H.; Jaafar, H.Z.E. The relationship of nitrogen and C/N ratio with secondary metabolites levels and antioxidant activities in three varieties of malaysian kacip fatimah (Labisia pumila Blume). Molecules 2011, 16, 5514–5526. [Google Scholar] [CrossRef]
  26. Ibrahim, M.H.; Jaafar, H.Z.; Rahmat, A.; Rahman, Z.A. Effects of nitrogen fertilization on synthesis of primary and secondary metabolites in three varieties of kacip fatimah (Labisia Pumila Blume). Int. J. Mol. Sci. 2011, 12, 5238–5254. [Google Scholar] [CrossRef]
  27. Ibrahim, M.H.; Jaafar, H.Z. Enhancement of leaf gas exchange and primary metabolites under carbon dioxide enrichment up-regulates the production of secondary metabolites in Labisia pumila seedlings. Molecules 2011, 16, 3761–3777. [Google Scholar] [CrossRef]
  28. Karimi, E.; Jaafar, H.Z.; Ahmad, S. Phytochemical analysis and antimicrobial activities of methanolic extracts of leaf, stem and root from different varieties of Labisa pumila Benth. Molecules 2011, 16, 4438–4450. [Google Scholar] [CrossRef]
  29. Lindroth, R.L.; Kinney, K.K.; Platz, C.L. Responses of diciduous trees to elevated CO2: Productivity, phytochemistry, and insect performance. Ecology 1993, 74, 763–777. [Google Scholar] [CrossRef]
  30. Vurro, E.; Bruni, R.; Bianchi, A.; Sanità, L. Elevated atmospheric CO2 decreases oxidative stress and increases essential oil yield in leaves of Thymus vulgaris grown in a mini FACE system. Environ. Exp. Bot. 2009, 65, 99–106. [Google Scholar] [CrossRef]
  31. Ibrahim, M.H.; Jaafar, H.Z.E. Photosynthetic capacity, photochemical efficiency and chlorophyll content of three varieties of Labisia pumila Benth. Exposed to open field and greenhouse growing conditions. Acta Physiol. Plant. 2011, 33, 2179–2185. [Google Scholar] [CrossRef]
  32. Felgines, C.; Texier, O.; Morand, C.; Manach, C.; Scalbert, A.; Régerat, F.; Rémésy, C. Bioavailability of the flavanone naringenin and its glycosides in rats. Am. J. Physiol. Gastrointest. L. 2000, 279, G1148–G1154. [Google Scholar]
  33. Ho, P.C.; Saville, D.J.; Coville, P.F.; Wanwimoluk, S. Content of CYP3A4 inhibitors, naringin, naringenin and bergapten in grapefruit and grapefruit juice products tomato. Pharm. Acta Helv. 2000, 74, 379–385. [Google Scholar] [CrossRef]
  34. Wang, Y.S.H.; Bunce, A.J.; Maas, L.J. Elevated carbon dioxide increases contents of antioxidant compounds in field-grown strawberries. J. Agric. Food Chem. 2003, 51, 4315–4320. [Google Scholar] [CrossRef]
  35. Malikov, V.M.; Yuledashev, M.P. Phenolic compounds of plants of the Scutellaria L. genus: Distribution, structure, and properties. Chem. Nat. Compd. 2002, 38, 358–406. [Google Scholar] [CrossRef]
  36. Ibrahim, M.H.; Jaafar, H.Z.E. Involvement of carbohydrate, protein and phenylanine ammonia lyase on up-regulation of production of secondary metabolites (total phenolics and flavonoid) in Labisia pumila (Blume) Fern-Vill (Kacip Fatimah) under high CO2 and different nitrogen levels. Molecules 2011, 16, 4172–4190. [Google Scholar] [CrossRef]
  37. Hilal, M.; Parrado, M.E.; Rosa, M.; Gallardo, M.; Orce, L.; Massa, E.D. Epidermal lignin deposition in quinoa cotyledons in response to UV-B radiation. Photochem. Photobiol. 2004, 79, 205–210. [Google Scholar] [CrossRef]
  38. Dennis, D.T.; Blakeley, S.D. Carbohydrate Metabolism. In Biochemistry and Molecular Biology of Plants; Buchanan, B.B., Gruisem, W., Jones, R.L., Eds.; American Society of Plant Physiologists: Rockville, MD, USA, 2000; pp. 630–675. [Google Scholar]
  39. Johnson, R.H.; Lincoln, D.E. Sagebrush carbon allocation patterns and grasshopper nutrition: The influence of CO2 enrichment and soil mineral limitation. Oecologica 1991, 87, 127–134. [Google Scholar] [CrossRef]
  40. Chabot, S.; Belrhlid, R.; Chenevert, R.; Pichie, Y. Hyphal growth promotion in vitro of 27 mycorrhizal fungus, Gigaspora margarita Becker & Hall, by the activity of structurally specific 28 flavonoid compounds under CO2 enriched condition. New Phytol. 1992, 122, 461–467. [Google Scholar] [CrossRef]
  41. Estiarte, M.; Penuelas, J.; Kimball, B.A.; Hendrix, D.L.; Pinter, P.J.; Wall, G.W.; Lam-orte, R.L.; Hunsaker, D.J. Free-air CO2 enrichment of wheat: Leaf flavonoid concentration throughout the growth cycle. Physiol. Plant. 1999, 105, 423–433. [Google Scholar] [CrossRef]
  42. Schwanz, P.; Kimball, B.A.; Idso, S.B.; Hendrix, D.L.; Polle, A. Antioxidants in sun and shade leaves of sour orange trees (Citrus aurantium) after long-term acclimation to elevated CO2. J. Exp. Bot. 1996, 47, 1941–1950. [Google Scholar] [CrossRef]
  43. Herrmann, K.M.; Weaver, L.M. The shikimate pathway. Ann. Rev. Plant Phys. Plant Mol. Biol. 1999, 50, 473–503. [Google Scholar] [CrossRef]
  44. Penuelas, J.; Estiarte, M. Can elevated CO2 affect secondary metabolism and ecosystem function? Trees 1998, 13, 20–24. [Google Scholar]
  45. Muzika, R.M. Terpenes and phenolics in response to nitrogen fertilization: A test of the carbon/nutrient balance hypothesis. Chemoecology 1993, 4, 3–7. [Google Scholar] [CrossRef]
  46. Fajer, E.D.; Bowers, M.D.; Bazaaz, F.A. The effects of nutrients and enriched CO2 environment on the production of carbon based allelochemicals in Plantago: A test of the carbon/nutrient balance hypothesis. Am. Nat. 1992, 140, 707–723. [Google Scholar]
  47. Meyer, S.; Cerovic, Z.G.; Goulas, Y.; Montpied, P.; Demotes, S.; Bidel, L.P.R.; Moya, I.; Dreyer, E. Relationship between assessed polyphenols and chlorophyll contents and leaf mass per area ratio in woody plants. Plant Cell Environ. 2006, 29, 1338–1348. [Google Scholar] [CrossRef]
  48. Winger, A.; Purdy, S.; Maclean, A.; Pourtau, N. The role of sugars in integrating environmental signals during the regulation of leaf senescence. New Phytol. 2006, 161, 781–789. [Google Scholar]
  49. Matros, A.; Amme, S.; Kettig, B.; Buck, S.G.H.; Sonnewald, U.Y.; Mock, H.P. Growth at elevated CO2 concentrations leads to modified profiles of secondary metabolites in tobacco cv. SamsumNN and to increased resistance against infection with potato virus Y. Plant Cell Environ. 2006, 29, 126–137. [Google Scholar] [CrossRef]
  50. Hartley, S.E.; Jones, C.G.; Couper, G.C.; Jones, T.H. Biosynthesis of plant phenolics compounds in elevated atmospheric CO2. Glob. Change Biol. 2000, 6, 497–506. [Google Scholar] [CrossRef]
  51. Frankel, E.N.; Huang, S.W.; Kanner, J.; German, J.B. Interfacial phenomena in the evaluation of antioxidants: Bulk oils versus emulsions. J. Agric. Food Chem. 1994, 42, 1054–1059. [Google Scholar] [CrossRef]
  52. Benzie, I.F.; Strain, J.F. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: The FRAP assay. Anal. Biochem. 1996, 239, 70–76. [Google Scholar] [CrossRef]
  53. Ibrahim, M.H.; Jaafar, H.Z.E.; Haniff, M.H.; Raffi, M.Y. Changes in growth and photosynthetic patterns of oil palm seedling exposed to short term CO2 enrichment in a closed top chamber. Acta Physiol. Plant. 2010, 32, 305–313. [Google Scholar] [CrossRef]
  54. Ibrahim, M.H.; Hawa, Z.E.J. Primary, secondary metabolites, H2O2, maliondialdehyde and photosynthetic responses of Orthosiphon stimaneus Benth. to different irradiance levels. Molecules 2012, 17, 1159–1176. [Google Scholar] [CrossRef]
  55. Crozier, A.; Lean, M.E.J.; McDonald, M.S.; Black, C. Quantitative analysis of the flavonoid content of commercial tomatoes, onions, lettuce, and celery. J. Agric. Food Chem. 1997, 45, 590–595. [Google Scholar] [CrossRef]
  56. Martinez-Tellez, M.A.; Lafuente, M.T. Effects of high temperature conditioning on ethylene, phenylalanine ammonia lyase, peroxidase and polyphenol oxidase in flavedo of chilled “Fortune” mandarin fruit. J. Plant Physiol. 1997, 150, 674–678. [Google Scholar] [CrossRef]
  57. Ibrahim, M.H.; Jaafar, H.Z.E.; Asmah, R.; Zaharah, A.R. Involvement of Nitrogen on Flavonoids, Glutathione, Anthocyanin, Ascorbic Acid and Antioxidant Activities of Malaysian Medicinal Plant Labisia pumila Blume (Kacip Fatima. Int. J. Mol. Sci. 2012, 13, 393–408. [Google Scholar]
  58. Ibrahim, M.H.; Hawa, Z.E.J. Reduced photoinhibition enhanced kacip fatimah (Labisia pumila Blume) secondary metabolites, phenyl alanine lyase and antioxidant activity. Int. J. Mol. Sci. 2012, 13, 5290–5306. [Google Scholar] [CrossRef]
  59. Ibrahim, M.H.; Jaafar, H.Z. Impact of elevated carbon dioxide on primary, secondary metabolites and antioxidant responses of Eleais guineensis Jacq. (Oil Palm) seedlings. Molecules 2012, 17, 5195–5211. [Google Scholar] [CrossRef]
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Jaafar, H.Z.E.; Ibrahim, M.H.; Karimi, E. Phenolics and Flavonoids Compounds, Phenylanine Ammonia Lyase and Antioxidant Activity Responses to Elevated CO2 in Labisia pumila (Myrisinaceae). Molecules 2012, 17, 6331-6347. https://doi.org/10.3390/molecules17066331

AMA Style

Jaafar HZE, Ibrahim MH, Karimi E. Phenolics and Flavonoids Compounds, Phenylanine Ammonia Lyase and Antioxidant Activity Responses to Elevated CO2 in Labisia pumila (Myrisinaceae). Molecules. 2012; 17(6):6331-6347. https://doi.org/10.3390/molecules17066331

Chicago/Turabian Style

Jaafar, Hawa Z.E., Mohd Hafiz Ibrahim, and Ehsan Karimi. 2012. "Phenolics and Flavonoids Compounds, Phenylanine Ammonia Lyase and Antioxidant Activity Responses to Elevated CO2 in Labisia pumila (Myrisinaceae)" Molecules 17, no. 6: 6331-6347. https://doi.org/10.3390/molecules17066331

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