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. 2021 Jul 30;12:710487. doi: 10.3389/fphar.2021.710487

Nutraceutical Study on Maianthemum atropurpureum, a Wild Medicinal Food Plant in Northwest Yunnan, China

Li Xu 1,2,†, Yizhou Wang 1,2,†, Yuanyuan Ji 1,2,3,4,†, Ping Li 1,2, Wujisiguleng Cao 1,2,3, Shibiao Wu 4, Edward Kennelly 4,5, Chunlin Long 1,2,3,*
PMCID: PMC8363226  PMID: 34393791

Abstract

Maianthemum atropurpureum (Franch) LaFrankie (Asparagaceae), called nibai in Tibetan or dongka in Drung or zhu-ye-cai in local Chinese, is a wild vegetable consumed by the Tibetan people and other ethnic groups in Northwest Yunnan, China. It is also a traditional medicinal plant used by different linguistic groups for antimicrobial purposes. However the nutritional and phytochemical compositions of this important medicinal food plant have not been well studied previously. In this study, the nutrient content for nibai was determined by the China National Standards (GB) methods, and the phytochemical analysis involved multiple chromatographic and spectral methods including LC-TOF-MS analysis. Dried nibai is a rich source of protein (ca. 24.6%), with 18 of the 21 common amino acids. The amino acid content of nibai can reach up to 17.9/100 g, with the essential amino acids as major contributors, corresponding to 42.3% of the total amino acids. Nibai contains rich mineral elements, dietary fiber, vitamins, β-carotene, carbohydrates, and lipids. The phytochemical content of nibai was examined by conventional isolation strategies, as well as HR-ESI-TOF-MS to detect and identify 16 compounds including nine steroid saponins and seven flavonoids. Among these compounds, uridine, adenosine, guanosine, and β-methyl-6-methyl-d-glucopyranoside were found from the genus Maianthemum for the first time. These results help to demonstrate that the local people’s practice of consuming Maianthemum atropurpureum is reasonable due to its high levels of vitamins, minerals, essential amino-acids, and phytochemicals. Nibai may be further developed in Tibet and surrounding regions, and beyond as a health food, nutraceutical, and/or dietary supplement product.

Keywords: Maianthemum atropurpureum, ethnic people, east Himalayas, nutraceutical profile, steroid saponins

Introduction

Wild edible plants play an important role in furthering food security and improving the nutrition in the diets of people around the world, especially in poor rural communities (Lulekal et al., 2011). The utilization of wild edible plants is receiving more and more attention, not only due to their health benefits but also the opportunities they may present to rural economies (Multari et al., 2016). In daily life, wild vegetables may be a significant source of nutrients, including minerals, vitamins, fiber, and essential amino acids which are critical for good health, but often their nutrient and phytochemical content are not well studied (Turan et al., 2003). Many edible plants are also considered medicinal herbs (Liu et al., 2018; Luo et al., 2019; Sarker and Oba, 2019a, Sarker and Oba, 2020a; Sarker and Oba, 2020b). Some wild vegetables are gaining more widespread popularity due to their unique flavors, colors, and potential health properties (Costa et al., 2013; Sarker and Oba, 2019b).

The ethnic groups including Nu, Dulong (Drung), Lisu, Yi, Pumi, Bai, Naxi and Tibetan as well in northwest Yunnan (including Nujiang, Diqing, Dali and Lijiang provinces) of China, reside at high elevation areas with mountains and deep valleys. To better survive in these extreme conditions, local ethnic people often turn to wild (uncultivated) plants to supplement their diet and therebey enrich their food diversity. Ahmad and Pieroni found that certain wild edible plants have been embraced by a particular local culture because of their traditionally acquired knowledge-based principles, feelings, and manners (Ahmad and Pieroni, 2016). Moreover, wild foods contribute to overcoming periods of famine, and dishes made of wild plants can be very healthy by providing local people with various essential nutritious elements, such as vitamins and minerals.

The local people in northwest Yunnan collect the young shoots (tender aerial parts) of a group of seven species in Maianthemum Web. for food, including M. atropurpureum (Franch.) LaFrankie, M. purpurea (Wall.) LaFrankie, M. oleracea (Baker) LaFrankie, M. tatsienense (Franch.) LaFrankie, M. forrestii (W.W. Sm.) LaFrankie, M. fuscum (Wall.) LaFrankie, and M. henryi (Baker) LaFrankie (Ju et al., 2012), belonging to the family Asparagaceae. Among them, M. atropurpureum is the most well-known, and considered to taste the best. Maianthemum atropurpureum (Franch.) LaFrankie, called nibai in Tibetan, dongka in Drung, zhu-ye-cai in local language, or gao-da-lu-yao in Mandarin, a flavorful seasonal wild vegetable with unique flavors. It grows at high attitude on mountains, and can be collected in May when the snow has just melted (Figure 1). It was one of the major vegetables consumed by local herdsmen in the Tea Horse Road trade route. The previous studies reported that everyday about 2 tons (2000 kg) of would be sold in a single market of a town in northwest Yunnan, while more Maianthemum atropurpureum (nibai) were collected and directly consumed by the local people (Gui et al., 2000a; Gui et al., 2000b). Now it is considered by Tibetan, Nu, Drung, Lisu, Bai, Yi, Pumi, and Naxi people as a delicacy used to celebrate festivals and entertain guests. There are many ways to prepare M. atropurpureum: the fresh shoots can be used in soups, stir-fried with pork, or eaten raw as salad, and the dried shoots can be served in wintertime hot pot dishes.

FIGURE 1.

FIGURE 1

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The plant of Maianthemum atropurpureum. (A) Wild habitat; (B) Shoots sold on market; (C) Mature leaves (photographed by the authors).

Maianthemum atropurpureum is also considered to be an excellent medicine for annealing, heat-clearing, detoxicating, and lowering blood pressure in traditional Chinese medicine practice. The rhizome, as a folk medicine, has been used to treat lung ailment, rheumatism, menstrual disturbance, mammitis, cuts, bruises, kidney diseases, and also to activate blood circulation and to alleviate pain (Jiang, 1977; State Administration of Traditional Chinese Medicine, 1999). The minerals, vitamins, essential amino-acids, carbohydrates and lipids in leaves of Maianthemum atropurpureum (nibai) have been preliminarily investigated (Gui et al., 2000a). In addition, steroid saponins, nucleosides and flavonoids, were isolated from nibai (Yang, 2003; Zhang et al., 2006; Yang et al., 2009).

Seven new steroidal saponins, atropurosides A–G, with new polyhydroxylated aglycones, were identified from the rhizomes of Maianthemum atropurpureum, together with a known saponin and dioscin. Among them, atropurosides B and F showed moderate inhibitory activity against Candida albicans, Candida glabrata, Cryptococcus neoformans, and Aspergillus fumigatus, while dioscin was more active against C. albicans and C. glabrata (Zhang et al., 2006). These three compounds are moderately cytotoxic. It appears that the antifungal activity of these steroidal saponins correlates with their cytotoxicity against mammalian cells (Zhang et al., 2006).

Thesecondary metabolites from young edible shoots of Maianthemum atropurpureum have not been reported. Further work on Maianthemum atropurpureum, therefore, is necessary since its bioactive constituents are not fully understood. Its nutritional composition also need to be re-examined based on modern standard techniques. This study investigated the nutritional content and chemical constituents of this typical medicinal and food plant valued by the Tibetan, Nu, Drung and other linguistic groups, and discuss its potential to be developed as new functional food or nutraceutical.

Materials and Methods

Samples and Sample Preparation

The aerial parts of Maianthemum atropurpureum (Franch.) LaFrankie were collected in Gongshan County, Nujiang Prefecture, NW Yunnan, China, in May 2013 and identified by Prof. Chun-Lin Long (Minzu University of China). The voucher specimen (No. 20130584) was deposited at the Herbarium of Minzu University of China. Some of the sample (300 g) was boiled with salt water and dried for the determination of nutrient content. The remaining sample (8.5 kg) was dried in the Sun directly for phytochemical studies.

Solvents, Reagents and Standards

The general laboratory solvents, including methanol (MeOH), ethanol (EtOH), petroleum ether (Pet), ethyl acetate (EtOAc), n-butyl alcohol (n-BuOH), acetone, chloroform (CHCl3), and dichloromethane (DCM) were of analytical grade and were purchased from Beijing Chemical Works (Beijing, China). Chromatography and extraction solvents (acetonitrile, methanol, formic acid) were of HPLC grade obtained from VWR Inc (Bridgeport, PA, United States). UPLC grade water was prepared by using the Millipore Milli-RO 12 system (Millipore, Bedford, United States). All pure isolated compounds were characterized by HR-ESI-MS, 1H NMR, and 13C NMR spectroscopic methods for identification purposes.

Determination of Proximate Composition

Percentages of moisture was determined by vacuum oven under 105°C for 2 h to constant weight per the China national standards (GB) method (GB 5009.3-2010) (Zhang et al., 2009). Ash was determined by direct analysis according to the China standards method (GB 5009.4-2010), the sample was fully carbonized with a low flame until no smoke was produced, and weighed. The dry sample was then placed in a muffle furnace to burn under 550 ± 25°C for 4 h, removed, and placed into a desiccator for 30 min after cooling down to 200°C. The whole process was repeated until to a constant weight (Nie et al., 2014). Total lipid content was determined by Soxhlet extraction using the China standards method (GB/T 5009.6-2003) (Wang et al., 2005; Liu et al., 2015). Protein content was determined by Kjeldahl nitrogen using the China standards method (GB/T5009.5-2010) (Zhang, 2008), and the percentage of crude protein was estimated as the total nitrogen content multiplied by the conversion factor 6.25. Total carbohydrates were calculated by subtracting the total percentage of other components (saccharides, starch and dietary fiber) from 100.

Determination of Dietary Fiber

Total fiber, soluble fiber, and insoluble fiber contents were determined by Dietary Fiber Determination System (VELP GDE + CSF6, Italian) using the GB/T 5009.88-2008 method (Zhou, 2014).

Determination of Minerals, Vitamins and β-carotene

Minerals, vitamins, and β-carotene were analyzed according to corresponding China standard methods GB/T (Wang et al., 2005), among which K, Na, Fe, Mn, Mg, Ca, Cu and Zn were determined using inductively coupled plasma-mass spectrometery (ICP-MS) (Wang et al., 2005); P and vitamin C were determined by ultra-violet and visible spectrophotometery (UVPC) (Wang et al., 2005); Cr was determined using an atomic absorption spectrometer (AAS) (Wang et al., 2005); vitamin A was determined using ultra performance liquid chromatography (UPLC) (Wang et al., 2005); vitamin B2 was determined using molecular fluorescence photometer (Wang et al., 2005). The determination of β-carotene was carried out by high-performance liquid chromatography (HPLC) as previously reported (Sun et al., 2009).

Determination of Amino Acids

Amino acids were measured according to the method GB/T 5009.124-2003 by Amino acid Analyzer (Hitachi L-8900, Japan) (Wang et al., 2005; Xing et al., 2012). Data were expressed as milligrams of amino acid per 100 g of nibai.

Isolation and Identification of Chemical Compounds

Dried and powdered samples of Maianthemum atropurpureum (nibai) (8.5 kg) were extracted five times with 70% EtOH under reflux to give an ethanol extract. After evaporation under reduced pressure, the extracted residue was suspended in water and partitioned successively with petroleum ether, ethyl acetate, and n-BuOH. The n-BuOH extract (109 g) was subjected to silica gel (200–300 mesh) column chromatography eluting with EtOAc-acetone gradient (1:0→0:1) and pooled based on TLC profiles to yield seven fractions (Fr.1-Fr.7). Fr.2 (3.24 g) was dissolved with MeOH, and the insoluble part was recrystallized with MeOH and gave compound 1. The soluble part was subjected to silica gel (200–300 mesh) column chromatography eluting with CH2Cl2-MeOH gradient (25:1→2:1) to yield Fr.2.3 and Fr.2.5. Fr.2.3 was purified by Sephadex LH-20 chromatography using MeOH as the eluent to yield compound 3. In addition, Fr.2.5 was repeated chromatographed by silica gel column under different gradient conditions with CH2Cl2-MeOH to give compounds 4, 5, and 7. The insoluble part in Fr.3 (3.01 g) was also recrystallized with MeOH and gave compound 2, and the soluble part was further purified by successive silica gel column chromatography with CH2Cl2-MeOH (20:1, 15:1, 10:1) followed by CH2Cl2-MeOH (15:1, 10:1), yielding 8 mg of compound 6. Fr.5 (4.47 g) was subjected to Si gel column chromatography with CH2Cl2-MeOH (18:1, 15:1, 10:1) and pooled based on TLC profiles to yield five fractions (Fr.5.1-Fr.5.5). Fr.5.3 was purified by silica gel column chromatography (15:1, 12:1) to yield compound 10. Fr.5.4 was repeated silica gel medium pressure liquid chromatography gradient eluted with a MeOH-H2O solvent system (5, 10, 20, 40, 60, and 100%), followed by preparative HPLC with 50% MeOH (MeOH-H2O) and further purified by silica gel column to yield compounds 8 and 9.

Liquid Chromatography Time-of-Flight Mass Spectrometry Analysis

LC-TOF-MS analysis of the n-BuOH extract was performed using a Waters (Milford, MA, United States) Alliance 2695 system equipped with 2695 separation module units and 2998 PDA detectors using a 100 mm × 2.0 mm, 2.5 µm Phenomenex Synergi Hydro-RP 100 A column with 3 mm × 4.0 mm Phenomenex Security Guard column (Torrance, CA United States). The mobile phase consisted of solvents (A) 0.1% aqueous formic acid solution and (B) acetonitrile using a stepwise gradient elution of 3% B for 5 min, 3%–15% B at 5–15 min, 15% B for 5 min, 15%–45% B at 21–35 min, 45%–90% B at 35–40 min, and this proportion of solvent kept for 10 min. The UV-Vis spectra were recorded from 190 to 700 nm. The flow rate and the injection volume were 0.2 ml/min and 10 μL, respectively. Both column and sample temperatures were 25°C. LC/MS-grade methanol was used to redissolve the freeze-dried sample, and then brought up to 2 mg/ml and filtered using 25 mm syringe filter (0.45 µm PTFE membrane) prior to injection.

High-resolution electrospray ionization time of flight mass spectrometry (HR-ESI-TOF-MS) was performed using an LCT Premier XE TOF mass spectrometer (Waters, Milford, MA) equipped with an ESI interface and controlled by Mass Lynx V4.1 software. Mass spectra were acquired in both positive and negative modes over range m/z 100–1500. The capillary voltages were set at 3000 V (positive mode) and 2700 V (negative mode), respectively, and the cone voltage was 30 V. Nitrogen gas was used for both the nebulizer and desolvation. The desolvation and cone gas flow rates were 600 and 20 L/h, respectively. The desolvation temperature was 400°C, and the source temperature was 120°C.

Results and Discussions

Nutrient Composition and Dietary Fiber

The nutrient composition and dietary fiber content of Maianthemum atropurpureum (Franch.) LaFrankie (nibai) are listed in Table 1. Insoluble dietary fiber was the predominant component (26.0/100 g), followed by protein (24.6/100 g), while carbohydrate and lipid contents were much lower. The dietary fiber content is comparable with that of fiddlehead fern (Pteridium aquilinum var. latiusculum) with 25.5/100 g, one of the most important wild food plants in China (Liu et al., 2012), and higher than that of spinach (Spinacia oleracea) with 12.7/100 g. The protein and carbohydrate content among three species are very different; nibai has the highest protein content (24.6/100 g), and the lowest carbohydrate content (23.8/100 g). The protein and carbohydrate content of nibai is much higher than different vegetable amaranth species, such as Amaranthus blitum (Sarker and Oba, 2020c), stem amaranth (Sarker et al., 2020a), green morph amaranth (Sarker et al., 2020b) and red morph amaranth (Sarker and Oba, 2019c).

TABLE 1.

Compositional and nutritional characteristics of zhu-ye-cai compared with other well-known edible greens. (Values per 100 g of zhu-ye-cai dried after boiling with salted water)

Parameters Unit zhu-ye-cai fiddleheada spinacha
Approximate composition
 Moisture G 7.22 nd Nd
 Ash G 13.5 nd Nd
 Crude lipid G 4.9 0.9 0.6
 Crude protein G 24.6 6.6 6.4
 Total carbohydrate G 23.8 54.2 63
Dietary fiber
 Total dietary fiber G 26.1 25.5 12.7
 Soluble dietary fiber (SDF) G 0.07 nd Nd
 Insoluble dietary fiber (IDF) G 26.0 nd Nd
Minerals
 K Mg 1800 59 919
 Na Mg 2490 20.4 242
 Ca Mg 252 851 411
 Mg Mg 231 82 183
 Fe Mg 20.3 23.7 25.9
 Mn Mg 5.98 2.31 1.61
 Zn Mg 4 18.11 3.91
 Cu Mg 6.62 2.79 2.08
 Cr Mg 0.84 nd Nd
 P Mg 313 253 222
Vitamins and β- carotene
 β-carotene Mg 7.95 nd Nd
 Vitamin A Mg 9.8 0 598
 Vitamin B2 Mg 0.2 nd Nd
 Vitamin C Mg 2 3 82
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a

From Chinese Food Composition Table.35.

All of these vegetables are dehydrated, and zhu-ye-cai is dried after boiling with salt water so the Sodium content is extremely high; nd means not detected (below the detection level).

Dietary fiber is indispensable to a healthy diet, and its health benefits have been known for decades (Le et al., 2016). In the gastrointestinal tract, dietary fibers can promote intestinal peristalsis to accelerate the removal of carcinogenic substances and toxic matter, and reduce bacterial growth. Dietary fiber can also help to reduce cholesterol levels, prevent obesity and chronic diseases (Patil et al., 2009). Dietary fiber significantly contributed to the cure of constipation, digestibility, and palatability (Sarker et al., 2020c; Sarker and Oba, 2020d; Sarker and Oba, 2020e). Nibai has a high content of protein, along with a low carbohydrate content, making it a potentially healthy food plant for people looking to reduce carbohydrate intake. With the growing obesity epidemic in developed nations, foods with high protein and diet fiber content, and low carbohydrate and lipid content has been advocated by certain nutritionists. Thus, nibai could potentially be considered a functional food which can meet the modern healthy diet requirement.

Minerals, Vitamins and β-Carotene

Ten minerals have been detected in nibai, and five of them are essential microelements of human body, including Fe, Zn, Cu, Cr, and Mg (Table 1). The content of Fe (20.3 mg/100 g) is comparable with that of spinach (25.9 mg/100 g) and fiddlehead (23.7 mg/100 g) which are commonly considered Fe-rich vegetables. However, it is much higher than commonly considered Fe rich Amaranthus hypochondriacus (Sarker and Oba, 2020d). The Mg, Cu and P levels in nibai are the highest, when compared to spinach and fiddlehead fern. Mg, Cu and P were much higher than vegetable amaranth (Sarker and Oba, 2020e). Zn levels in nibai are similar to spinach, but both are significantly lower than fiddlehead. However, Zn content was much lower than vegetable amaranth (Sarker et al., 2020c). It has been estimated that half the world’s population is iron deficient (Karakoy et al., 2012). Therefore, nibai could be a very useful dietary source for Fe and other nutrients to help maintain good health for people with certain nutrient deficiencies. Vitamins serve many physiological functions and are of the essence to maintain health. Compared with spinach and vegetable amaranth, the contents of vitamins A, B2, and C in nibai are lower, but it is still an important source of vitamins for Tibetans and other linguistic groups through the famine and the food shortages caused by the extreme environment. Consuming nibai contribute to prevent vitamins and trace elements deficiencies and maintain the normal bodily functions.

Amino Acids

The 18 amino acids identified and quantified in nibai are presented in Table 2, in which eight are essential to humans. Tryptophan was detected in nibai for the first time (Gui et al., 2000a; Gui et al., 2000b). The total amino acid content is up to 17.9 g/100 g, and the percentage of essential amino acids in total amino acids (E/T) reach up to 42.29%, which is higher than that of soybean (33%). According to the ideal model proposed by WHO/FAO, the ratio of E/T of good quality protein is about 40%, and the ratio of E/N (the percentage of essential amino acids to nonessential amino acid) is above 60% (Zhang et al., 2013). The composition of amino acid of nibai meets this ideal model. Additionally, the content of glutamic acid is the highest (2.98 g/100 g), followed by aspartic acid (1.73 g/100 g), leucine (1.71 g/100 g), lysine (1.32 g/100 g), and alanine (1.29 g/100 g), respectively.

TABLE 2.

Amino acids of zhu-ye-cai (Values per 100 g of zhu-ye-cai dried after boiling with salted water).

Amino acids unit zhu-ye-cai
Aspartic acid (Asp) g 1.73
Threonine (Thr)* g 0.73
Serine (Ser) g 0.74
Glutamate (Glu) g 2.98
Proline (Pro) g 0.64
Glycine (Gly) g 0.9
Alanine (Ala) g 1.29
Cystine (Crs) g 0.26
Valine (Val)* g 1.24
Methionine (Met)* g 0.11
Isoleucine (Ile)* g 1.09
Leucine (Leu)* g 1.71
Tyrosine (Tyr) g 0.41
Phenylalanine (Phe)* g 1.16
Lysine (Lys)* g 1.36
Histidine (His) g 0.34
Tryptophan (Try)* g 0.17
Arginine (Arg) g 0.92
Essential amino acids(E) g 7.57
Total amino acids(T) g 17.9
E/T % 42.29
Lys/T % 7.59
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Note * indicates essential amino acids.

Glutamate and arginine play important roles in regulating gene expression, cell signaling, antioxidative responses, and immunity (Wu, 2010). Our work showed that nibai is a good source of amino acids, which can provide indigenous people with nearly all the amino acids that humans require. Four amino acids in nibai, aspartic acid and glutamate contribute to its umami taste, while glycine and alanine contribute to its sweet taste (Bu et al., 2013). The total content of these four amino acids in nibai was 6.9 g/100 g, accounting for 38.6% of the total amino acids, these four amino acid contribute a characteristic taste to the flavor of nibai.

Phytochemical Constituents

Sixteen compounds were detected and tentatively identified using a method based on HPLC coupled with both PDA and HR-ESI-TOF-MS. The TIC chromatography of the n-BuOH extract of M. atropurpureum is displayed in the supplementary material (DataSheet 1). Their retention times, UV spectra, and exact mass spectral fragmental ions in positive and negative modes are shown in Table 3, and compared with literature values. Furthermore, the molecular formula was calculated based upon fragment ion peak data along with previous reports in SciFinder and other databases. The structures of part selected compounds are shown in Figure 2.

TABLE 3.

LC-MS-TOF data of the compounds identified from the n-butonal extract of Maianthemum atropurpureum.

No R.T. (min) UV [M + H]+ or [M-H]- (M.F., ppm) Adduct and fragmental ion exact masses [M-X]+ or [M-X]- (M.F., ppm) Identification References
8 8.3 230, 256 611.1619 [M + H]+ (C27H31O16, 1.1) 633.1429 [M + Na]+ (C27H30O16 Na,-0.5); 465.1053 [M + H-146(Rha)]+ (C21H21O12, 4.3) Rutin Kaneta et al. (1980)
609.1428 [M-H]- (C27H29O16, -4.6) 655.1569 [M-H + HCOOH]- (C28H31O18, 9.0)
9 10.5 230, 256 465.1055 [M + H]+(C21H21O12, 4.7) 303.0497 [M + H- Glc]+ (C15H11O7,−2.6); 487.0862 [M + Na]+ (C21H20O12Na, 2.1) Quercetin 3-O-galactoside Kaneta et al. (1980)
463.0916 [M-H]- (C21H19O12, 8.4) —
10 13.1 230, 256 611.1620 [M + H]+(C27H31O16, 1.3) 633.1478 [M + Na]+(C27H30O16 Na,7.3); 465.1027 [M + H-146(Rha)]+ (C21H21O12, -1.3); 303.0521 [M + H-Rha-Glc]+(C15H11O7, -1.3) Quercetin 3-O-glucoside 7-O-rhamnoside Kaneta et al. (1980)
609.1505 [M-H]- (C27H29O16, 8.0) 655.1569 [M-H + HCOOH]- (C28H31O18, 9.0)
11 13.6 230, 256 625.1740 [M + H]+(C28H33O16,-4.6) 479.1211 [M-Rha + H]+ (C22H23O12,4.4); 317.0660 [M-Rha-Glc + H]+ (C16H13O7,-0.3); 647.1553 [M + Na]+(C28H32O16Na, -5.4) Isorhamnetin-3-Rutinoside El-Alfy et al. (1975)
623.1763 [M-H]-(C28H31O16,- 0.3) 669.1641 [M-H + HCOOH]- (C29H33O18,-3.9)
12 14.6 — 755.4235 [M + H]+(C39H63O14,2.3) 593.3706 [M-Glc + H]+ (C33H53O9,2.7); 27-epi-Trikamsteroside A Yokosuka et al. (2008)
13 15.0 — — 871.4673 [M-H2O + H]+(C44H71O17, −2.1); 793.4024 [M-Xyl+2H2O + H]+ (C39H69O16,1.3); 725.4124 [M-Rha-H2O + H]+ (C38H61O13,1.7); 593.3668 [M- Xyl-Rha- H2O + H]+ (C35H53O9, −3.7); 413.3078 [M- Xyl-Rha-Gal- 2H2O + H]+(C27H41O3,5.3); 911.4673 [M + Na]+ (C44H72O18Na, 6.3) (3β,5α,6β,25R)-spirostane-3,5,6-triol-3-O-β-D-apiofuranosyl-(1→ 3)-[α-l-rhamnopyranosyl-(1→2)]- β-D-glucopyranoside Wu et al. (2012)
887.4696 [M-H]- (C44H71O18, 6.3) 933.4628 [M-H + HCOOH]-(C45H73O20,-7.2)
14 15.9 — 901.4814 [M + H]+(C45H73O18,1.9) 923.4615 [M + Na]+ (C45H72O18 Na, −0.1); 739.4250 [M -Glc + H]+(C39H63O13, −2.6); 577.3737 [M-2Glc- + H]-(C33H53O8, −0.5) Funkioside D Yang et al. (2009)
— 899.4673 [M-H]- (C45H71O18,3.7) 945.4709 [M-H + HCOOH]- (C46H75O20,1.5) — —
15 16.8 — — 885.4833 [M + H-H2O]+(C45H73O17, −1.7); 739.4282 [M -Rha- H2O + H]+(C39H63O13, 1.8); 577.3737 [M-Gal-Rha- H2O + H]+(C33H53O8, −0.5); 415.3230 [M-Gal-Glc-Rha-H2O + H]+ (C27H43O3, 4.3); 925.4753 [M + Na]+ (C45H74O18Na, −2.2) Slimacinoside C Yang et al. (2009)
— 901.4769 [M-H]- (C45H73O18, −3.1) 947.4926 [M-H + HCOOH]- (C46H75O20, 7.8) — —
16 17.7 230, 256 303.0494 [M + H]+(C15H11O7, -3.6) — Quercetin Zhao et al. (2009)
— 301.0342 [M-H]- (C15H9O7, -2.0) — — —
17 17.9 230, 256 287.0549 [M + H]+(C15H11O6, -2.4) — Luteolin Zhao et al. (2009)
— 285.0405 [M-H]- (C15H9O6, 2.1) — — —
18 18.1 — — 739.4282 [M-Rha- H2O + H]+(C39H63O13, 0.0); 577.3745 [M-Gal-Rha-H2O + H]+ (C33H53O8,0.9); 415.3211 [M-Gal-Glc-Rha- H2O + H]+ (C27H43O3, −0.2); 397.3138 [M-Gal-Glc-Rha- H2O + H]+ (C27H43O3, −0.2); 925.4819 [M + Na]+ (C45H74O18Na, 5.0) (3β,22α)-26-(β-D-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl2-O-(6-deoxy-α-L-mannopyranosyl) -β-D-glucopyranoside
— 901.4828 [M-H]- (C45H73O18, 3.4) 947.4926 [M-H + HCOOH]- (C46H75O20, 7.8) — —
19 18.7 230, 256 — 353.4832 [M + Na]+ (C22H35 O2 Na, 3.9) 1-Phenanthren-emethanol Kitajima et al. (1982)
— 329.4812M-H]- (C22H33O2, −2.1) — — —
20 18.9 230, 256 885.4838 [M + H]+(C45H73O17,-1.1) 907.4659 [M + Na]+ (C45H72O17Na, −0.9); 739.4293 [M-Rha + H]+(C39H63O13, 3.2); 577.3766 [M-Glc-Rha + H]+(C33H53O8, 4.5); 415.3199 [M-2Glc-Rha + H]+ (C27H43O3, −3.1) Gracillin Inoue et al., 1995; Zhao et al., 2011
— 883.4691 [M-H]- (C45H71O17, -4.0) 929.4808 [M-H + HCOOH]- (C46H73O19, 6.7) — —
21 19.7 — — 355 [M + Na]+ (C22H37 O2 Na, −3.4) Ent-kaur-15-en-17-ol Kitajima et al. (1982)
— 331 [M-H]- (C22H35O2,1.9) — —
22 19.9 230, 256 301.0717 [M + H]+ (C16H13O6, 1.7) — 5,7,4′-trihydroxy-3′-methoxyflavone Zhao et al. (2009)
— 299.0573 [M-H]- (C16H11O6, 5.7) 345.0599 [M-H + HCOOH]- (C17H13O8, −3.2) — —
23 20.9 — — 577.3740 [M-H2O + H]+(C33H63O8, 6.8); 617.3685 [M + Na]+ (C33H54O9Na,3.1) 26-O-β-D-glucopyranosyl-(25R)-furost-5-ene-3β, 22ξ, 26-triol Wu et al., 2012
— 593.3697 [M-H]- (C33H53O9, 1.2) 639.3683 [M-H + HCOOH]- (C34H55O11, −9.5) — —
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FIGURE 2.

FIGURE 2

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Structures of seven compounds isolated from Maianthemum atropurpureum. Thymidine (A), uridine (B), adenosine (C), guanosine (D), 2-Phenylethyl-β-D-glucopyranoside (E), β-methyl-6-methyl-D-glucopyranoside (F), isorhamnetin-3-O-robinobioside (G).

Seven known compounds (Figures 2A–G) have been isolated using conventional column chromatography and elucidated on the basis of detailed spectroscopic analyses from nibai, including thymidine 1) (Yang and Liu, 2003), uridine 2) (Gong and Ding, 2005), adenosine 3) (Yang and Liu, 2003), guanosine 4) (Gong and Ding, 2005), 2-phenylethyl- β-D-glucopyranoside 5) (Kim et al., 2008), β-methyl-6-methyl-d-glucopyranoside 6) (Gong and Ding, 2005), and isorhamnetin-3-O-robinobioside 7) (Wang et al., 2010). Among them, compounds 2, 3, 4, 6 were found from the genus Maianthemum for the first time.

More compounds had been identified from Maianthemum atropurpureum comparing with current literatures (Yang and Liu, 2003; Gong and Ding, 2005; Kim et al., 2008). In particular, four compounds including uridine, adenosine, guanosine, and β-methyl-6-methyl-d-glucopyranoside had not been reported from Maianthemum in any previous references. Our methods adopted for isolating chemical compounds may be more appropriate.

Thymidine 1) was isolated as colorless acicular crystal. All NMR data are in agreement with literature data (Yang and Liu, 2003). The molecular formula was obtained via ESI-MS and deduced as C10H14N2O5 (observed m/z at 243 [M + H]+ (calcd for C10H14N2O5, 243). The identification of uridine 2) which was isolated as colorless acicular crystal was confirmed by comparing the 13C NMR data with literature and database values (Gong and Ding, 2005). ESI-MS m/z 245 [M + H]+, C9H12N2O6. Compared with that of 1, upfield shifts in the C-5 and C-2′ indicated that there was no methyl substitute group, but with ribose connected. Based on these data, compound 2 was identified as uridine. Adenosine 3) was white powder; 1H NMR and 13C NMR were in agreement with literature values. ESI-MS m/z 267 [M + H]+ (calcd for C10H13N5O4, 267) corresponded with those reported in the literature (Yang and Liu, 2003). Guanosine 4) was identified as white powder; 1H NMR and 13C NMR were in agreement with the literature (Gong and Ding, 2005); ESI-MS m/z 283 [M + H]+ (calcd for C10H13N5O5, 283) and was identical to literature data (Gong and Ding, 2005). 2-Phenylethyl-β-d-glucopyranoside 5) was gummy, colorless, solid; 1H NMR13C-NMR are in agreement with published values. ESI-MS m/z 285 [M + H]+ (calcd for C14H20O6, 285) was identical to literature data (Kim et al., 2008). β-methyl-6-methyl-d-glucopyranoside 6) was white powder; 13C NMR (75 MHz, MeOD): δ 103.5 (C-1), 78.2 (C-3), 74.1 (C-5), 73.7 (C-2), 72.5 (C-6), 71.9 (C-4), 66.5 (C6-OCH 3), 64.5(C1-OCH 3); ESI-MS m/z 208 [M] (calcd for C8H16O6). Comparing with NMR database, the 13C NMR data showed 75% similarity to that of ethyl-β-D-fructopyranoside, from which the hydroxyl substituent fructose was confirmed. The 1H NMR spectrum of 6 showed the presence of six hydrogens at δ1.74 and 2 carbons at δ 66.5 and 64.5, pointing to the existence of two methoxy groups. Comparing all the carbon chemical shift data of β-methyl-d-glucopyranoside with 6-O-methyl-β-d-glucopyranoside, the data were in agreement with those obtained from the literature data (Gong and Ding, 2005). Therefore, 6 was identified as β-methyl-6-methyl-d-glucopyranoside. Isorhamnetin-3-O-robinobioside (7): pale yellow crystal; 1H NMR and 13C NMR are in agreement with published data (Kaneta et al., 1980), ESI-MS m/z 467 [M + Na]+ (calcd for C28H32O16, 467) (Wang et al., 2010).

Biological Activities

The biological activities of nibai are attributed to its diverse bioactive components, especially the main constituents. According to this study and previous literature, the primary chemical components of M. atropurpureum are steroid saponins, nucleosides, and flavonoids, especially the large polarity constituents, some of which have considerable biological activities. For instance, the smilacinoside A, aspidistrin, and funkioside D isolated from the aerial parts of M. atropurpureum exhibited prominent activity in vitro cytotoxicity against K562 tumor cell line with IC50 values of 1.09, 0.47, and 2.93 μg/ml, respectively (Yang et al., 2009). Nucleosides also exerted a variety of biological activities, such as antitumor (Ogawa et al., 1998), antivirus (Ruth and Cheng, 1981) and gene therapy effects (Parker et al., 1997). Thymidine, for instance, is the nucleus of stavudine and zidovudine which are both anti-AIDS drugs (Ross et al., 2001). Moreover, adenosine has a range of significant pharmacological effects, including making blood vessels diastolic, lowering blood pressure, slowing heart rate, inhibiting platelet gathering, relaxing vascular smooth muscle, improving cardio-cerebral blood circulation, preventing arrhythmia, inhibiting the release of neurotransmitters, and adjusting the activities of adenosine activation enzyme (Layland et al., 2014). Flavonoids, such as rutin, quercetin, luteolin, and their glycosides are the most common and widely distributed group of plant phenolics (Sarker and Oba, 2018a; Sarker and Oba, 2018b). Many studies have demonstrated their antioxidant, scavenging free radical, anti-inflammatory, antibacterial, antiviral, and immunomodulatory effects (Sarker and Oba, 2020f; Sarker and Oba, 2020g; Sarker and Oba, 2021). All of these bioactive constituents as well as vitamin C, β-carotene and several minerals (Fe, Zn, and Mn), along with amino acids have contributed to nibai’s medicinal effects and thus demonstrate the current utilization of this wild plant to treat diseases and enhance immunity in humans.

Many studies have correlated diet and certain chronic diseases such as cancer, cardiovascular disease, diabetes, and osteoporosis. Bioactive compounds from edible plants have the potential to prevent certain chronic conditions (Patil et al., 2009; Sarker and Oba, 2018c; Sarker and Oba, 2018d; Sarker and Oba, 2018e). Nibai, dongka or zhu-ye-cai (M. atropurpureum), an endemic species to the Hengduan Mountains, is a less common wild vegetable rich in nutrient and phytochemical content. It plays an important role not only in providing local Tibetans and other linguistic groups with various essential nutrition elements, but may also contribute to maintaining health, promoting immunity, and preventing several kinds of diseases. Consequently, nibai can be considered a promising new functional health food and/or nutraceutical.

Acknowledgments

We are very grateful to the staff of the PONY Testing Company (Beijing) for testing nutritional ingredients. Special thanks go to all informants of NW Yunnan, especially the collectors, retailers and restaurateurs in Diqing Tibetan Autonomous Prefecture and Nujiang Lisu Autonomous Prefecture for their unreserved information and patience, and Ms. Yan Ju from College of Life and Environmental Sciences, Minzu University of China.

Data Availability Statement

The datasets presented in this article are not readily available because, All datasets had been included in the paper. Requests to access the datasets should be directed to long@mail.kib.ac.cn or long.chunlin@muc.edu.cn.

Ethics Statement

Prior Informed Consent was obtained before collecting information related to traditional knowledge of Maianthemum from local people in northwest Yunnan.

Author Contributions

LX, YW, and YJ equally contributed to the article. LX: Investigation, Writing-original Draft. YW and YJ: Methodology, Data curation, Investigation, Formal analysis, Writing-Editing. PL, WC, SW, and EK: Validation, Writing-Review and Editing. CL: Conceived the study, Writing-Review and Editing, Supervision.

Funding

This work was supported by the Minzu University of China (No. 2020MDJC03), the Biodiversity Survey and Assessment Project of the Ministry of Ecology and Environment of China (No. 2019HJ2096001006), the National Natural Science Foundation of China (Nos. 31761143001 and 31870316) and the Ministry of Education of China (No. B08044).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2021.710487/full#supplementary-material

Click here for additional data file. (1.4MB, PDF)

Abbreviations

GB, national standard method of the people’s republic of China (initial of Guo Biao); MS/MS, mass spectrometry/mass spectrometry; NMR, nuclear magnetic resonance; PDA, photo-diode array; HR-ESI-TOF-MS, high resolution electrospray ionization time-of-flight mass spectrometry; TIC, total ion currency chromatograms; ESI-MS, electrospray ionization mass spectrometry; LC-TOF-MS, liquid chromatography time-of-flight mass spectrometry; MFCs, minimum fungicidal concentrations.

References

  1. Ahmad K., Pieroni A. (2016). Folk Knowledge of Wild Food Plants Among the Tribal Communities of Thakht-E-Sulaiman Hills, North-West Pakistan. J. Ethnobiol. Ethnomedicine 12, 17–32. 10.1186/s13002-016-0090-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bu J. Z., Dai Z. Y., Li Y., Wang H. H., Zhao Q. L., Jiang Q. Q. (2013). Analysis of Nutritional and Flavor Compounds in Crab Boiled Liquid. J. Chin. Inst. Food Sci. Tech. 9, 207–216. 10.13386/j.issn1002-0306.2017.03.003 [DOI] [Google Scholar]
  3. Costa A. G. V., Garcia-Diaz D. F., Jimenez P., Silva P. I. (2013). Bioactive Compounds and Health Benefits of Exotic Tropical Red-Black Berries. J. Funct. Foods 5, 539–549. 10.1016/j.jff.2013.01.029 [DOI] [Google Scholar]
  4. El-Alfy T. S., Paris R. R. (1975). On the Flavonoids of Ruscus Hypoglossum L. (Liliaceae). Pl. Med. Phytother. 9, 308–314. [Google Scholar]
  5. Gong Y. H., Ding L. S. (2005). Analysis of Natural Products. Kunming: Yunnan Science and Technology Press, 856–947. [Google Scholar]
  6. Gui M. Y., Chen B., ShenJ., Tian Y. S. (2000a). The Nutritional Value of Maianthemum Atropurpurea and its Exploitation. Guihaia 20, 71–74. [Google Scholar]
  7. Gui M. Y., Li Z. J., Chen B., Shen J., Tian Y. S. (2000b). The Compare of the Sample of Different Treatment Procedures to the Nutrition Contents of Similacina Atropurpurea . J. Jishou Univ. 21 (2), 55–57. [Google Scholar]
  8. Inoue K., Kobayashi S., Noguchi H., Sakawa U., Ebizuka Y. (1995). Spirostanol and Furostanol Glycosides of Costus Speciosus (Koenig.). SM. Nat. Med. 49, 336–339. [Google Scholar]
  9. Jiang S. X. (1977). Traditional Chinese Medicine. Shanghai: Shanghai People’s Publishing House, 754. [Google Scholar]
  10. Ju Y., Zhuo J., Liu B., Long C. (2013). Eating from the Wild: Diversity of Wild Edible Plants Used by Tibetans in Shangri-La Region, Yunnan, China. J. Ethnobiol. Ethnomedicine 9, 28–176. 10.1186/1746-4269-9-28 [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kaneta M., Hikichi H., Endo S., Sugiyama N. (1980). Identification of Flavones in Thirteen Liliaceae Species. Agric. Biol. Chem. 44, 1405–1406. 10.1080/00021369.1980.1086413810.1271/bbb1961.44.1405 [DOI] [Google Scholar]
  12. Karaköy T., Erdem H., Baloch F. S., Toklu F., Eker S., Kilian B., et al. (2012). Diversity of Macro- and Micronutrients in the Seeds of Lentil Landraces. Scientific World J. 2012, 1–9. 10.1100/2012/710412 [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kim K. H., Lee K. H., Choi S. U., Kim Y. H., Lee K. R. (2008). Terpene and Phenolic Constituents of Lactuca Indica L. Arch. Pharm. Res. 31, 983–988. 10.1007/s12272-001-1256-8 [DOI] [PubMed] [Google Scholar]
  14. Kitajima J., Komori T., Kawasaki T. (1982). Studies on the Constituents of the Crude Drug "Fritillariae bulbus." III. On the Diterpenoid Constituents of Fresh Bulbs of Fritillaria Thunbergii Miq. Chem. Pharm. Bull. 30, 3912–3921. 10.1248/cpb.30.3912 [DOI] [Google Scholar]
  15. Layland J., Carrick D., Lee M., Oldroyd K., Berry C. (2014). Adenosine. JACC: Cardiovasc. Interventions 7, 581–591. 10.1016/j.jcin.2014.02.009 [DOI] [PubMed] [Google Scholar]
  16. Le Gall S., Even S., Lahaye M. (2016). Fast Estimation of Dietary Fiber Content in Apple. J. Agric. Food Chem. 64, 1401–1405. 10.1021/acs.jafc.5b05301 [DOI] [PubMed] [Google Scholar]
  17. Liu Y. L., Hu W. Z., Jiang A. L., Liu C. H., Bai L. L. (2015). Determination of Fat and Fatty Acid in Chili and Chili Processing Food. Sci. Tech. Food Ind. 36, 285–291. 10.13386/j.issn1002-0306.2015.01.051 [DOI] [Google Scholar]
  18. Liu Y., Liu Q., Li P., Xing D., Hu H., Li L., et al. (2018). Plants Traditionally Used to Make Cantonese Slow-Cooked Soup in China. J. Ethnobiol. Ethnomedicine 14, 4. 10.1186/s13002-018-0206-y [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Liu Y. N., Liang Y., Wang G. J. (2014). Pharmacokinetics Research on Ophiopogonins Components in Ophiopogon Japonicus Extract. Chin. J. Experim. Tradit. Med. Formul. 20, 137–142. 10.13422/j.cnki.syfjx.2014090137 [DOI] [Google Scholar]
  20. Liu Y., Wujisguleng W., Long C. (2012). Food Uses of Ferns in China: a Review. Acta Soc. Bot. Pol. 81, 263–270. 10.5586/asbp.2012.046 [DOI] [Google Scholar]
  21. Lulekal E., Asfaw Z., Kelbessa E., Van Damme P. (2011). Wild Edible Plants in Ethiopia: a Review on Their Potential to Combat Food Insecurity. Af 24, 71–121. 10.21825/af.v24i2.4998 [DOI] [Google Scholar]
  22. Luo B., Li F., Ahmed S., Long C. (2019). Diversity and Use of Medicinal Plants for Soup Making in Traditional Diets of the Hakka in West Fujian, China. J. Ethnobiol. Ethnomedicine 15, 60. 10.1186/s13002-019-0335-y [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Multari S., Neacsu M., Scobbie L., Cantlay L., Duncan G., Vaughan N., et al. (2016). Nutritional and Phytochemical Content of High-Protein Crops. J. Agric. Food Chem. 64, 7800–7811. 10.1021/acs.jafc.6b00926 [DOI] [PubMed] [Google Scholar]
  24. Nie X. L., Sun W., Xu C. X. (2014). The Applicability of Two Methods for Ash Determination in Food. J. Food Saf. Qual. 5, 925–928. 10.19812/j.cnki.jfsq11-5956/ts.2014.03.051 [DOI] [Google Scholar]
  25. Ogawa A., Tanaka M., Sasaki T., Matsuda A. (1998). Nucleosides and Nucleotides. 180. Synthesis and Antitumor Activity of Nucleosides that Have a Hydroxylamino Group Instead of a Hydroxyl Group at the 2'- or 3'-Position of the Sugar Moiety1. J. Med. Chem. 41, 5094–5107. 10.1002/chin.19991724310.1021/jm980466g [DOI] [PubMed] [Google Scholar]
  26. Parker W. B., King S. A., Allan P. W., Bennett L. L., Secrist J. A., Montgomery J. A., et al. (1997). In VivoGene Therapy of Cancer withE. coliPurine Nucleoside Phosphorylase. Hum. Gene Ther. 8, 1637–1644. 10.1089/hum.1997.8.14-1637 [DOI] [PubMed] [Google Scholar]
  27. Patil B. S., Jayaprakasha G. K., Chidambara Murthy K. N., Vikram A. (2009). Bioactive Compounds: Historical Perspectives, Opportunities, and Challenges. J. Agric. Food Chem. 57, 8142–8160. 10.1021/jf9000132 [DOI] [PubMed] [Google Scholar]
  28. Ross L., Scarsella A., Raffanti S., Henry K., Becker S., Fisher R., et al. (2001). Thymidine Analog and Multinucleoside Resistance Mutations Are Associated with Decreased Phenotypic Susceptibility to Stavudine in HIV Type 1 Isolated from Zidovudine-Naive Patients Experiencing Viremia on Stavudine-Containing Regimens. AIDS Res. Hum. Retroviruses 17, 1107–1115. 10.1089/088922201316912718 [DOI] [PubMed] [Google Scholar]
  29. Ruth J. L., Cheng Y. C. (1981). Nucleoside Analogues with Clinical Potential in Antivirus Chemotherapy. The Effect of Several Thymidine and 2'-deoxycytidine Analogue 5'-triphosphates on Purified Human (Alpha, Beta) and Herpes Simplex Virus (Types 1, 2) DNA Polymerases. Mol. Pharmacol. 20, 415–422. 10.0000/PMID6272095 [DOI] [PubMed] [Google Scholar]
  30. Sarker U., Hossain M. M., Oba S. (2020b). Nutritional and Antioxidant Components and Antioxidant Capacity in green Morph Amaranthus Leafy Vegetable. Sci. Rep. 10, 1336. 10.1038/s41598-020-57687-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Sarker U., Hossain M. N., Iqbal M. A., Oba S. (2020c). Bioactive Components and Radical Scavenging Activity in Selected advance Lines of Salt-Tolerant Vegetable Amaranth. Front. Nutr. 7, 587257. 10.3389/fnut.2020.587257 [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Sarker U., Islam M. T., Oba S. (2018e). Salinity Stress Accelerates Nutrients, Dietary Fiber, Minerals, Phytochemicals and Antioxidant Activity in Amaranthus Tricolor Leaves. PLoS ONE 13, e0206388. 10.1371/journal.pone.0206388 [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Sarker U., Oba S. (2019a). Antioxidant Constituents of Three Selected Red and green Color Amaranthus Leafy Vegetable. Sci. Rep. 9, 18233. 10.1038/s41598-019-52033-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Sarker U., Oba S. (2018b). Augmentation of Leaf Color Parameters, Pigments, Vitamins, Phenolic Acids, Flavonoids and Antioxidant Activity in Selected Amaranthus Tricolor under Salinity Stress. Sci. Rep. 8, 12349. 10.1038/s41598-018-30897-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Sarker U., Oba S. (2021). Color Attributes, Betacyanin, and Carotenoid Profiles, Bioactive Components, and Radical Quenching Capacity in Selected Amaranthus Gangeticus Leafy Vegetables. Sci. Rep. 11, 11559. 10.1038/s41598-021-91157-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Sarker U., Oba S., Daramy M. A. (2020a). Nutrients, Minerals, Antioxidant Pigments and Phytochemicals, and Antioxidant Capacity of the Leaves of Stem Amaranth. Sci. Rep. 10, 3892. 10.1038/s41598-020-60252-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Sarker U., Oba S. (2018a). Drought Stress Enhances Nutritional and Bioactive Compounds, Phenolic Acids and Antioxidant Capacity of Amaranthus Leafy Vegetable. BMC Plant Biol. 18, 258. 10.1186/s12870-018-1484-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Sarker U., Oba S. (2020f). Leaf Pigmentation, its Profiles and Radical Scavenging Activity in Selected Amaranthus Tricolor Leafy Vegetables. Sci. Rep. 10, 18617. 10.1038/s41598-020-66376-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Sarker U., Oba S. (2019b). Nutraceuticals, Antioxidant Pigments, and Phytochemicals in the Leaves of Amaranthus Spinosus and Amaranthus Viridis Weedy Species. Sci. Rep. 9, 20413. 10.1038/s41598-019-50977-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Sarker U., Oba S. (2020e). Nutraceuticals, Phytochemicals, and Radical Quenching Ability of Selected Drought-Tolerant advance Lines of Vegetable Amaranth. BMC Plant Biol. 20, 564. 10.1186/s12870-020-02780-y [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Sarker U., Oba S. (2020c). Nutrients, Minerals, Pigments, Phytochemicals, and Radical Scavenging Activity in Amaranthus Blitum Leafy Vegetables. Sci. Rep. 10, 3868. 10.1038/s41598-020-59848-w [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Sarker U., Oba S. (2020d). Nutritional and Bioactive Constituents and Scavenging Capacity of Radicals in Amaranthus Hypochondriacus. Sci. Rep. 10, 19962. 10.1038/s41598-020-71714-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Sarker U., Oba S. (2020a). Phenolic Profiles and Antioxidant Activities in Selected Drought-Tolerant Leafy Vegetable Amaranth. Sci. Rep. 10, 18287. 10.1038/s41598-020-71727-y [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Sarker U., Oba S. (2020b). Polyphenol and Flavonoid Profiles and Radical Scavenging Activity in Leafy Vegetable Amaranthus Gangeticus . BMC Plant Biol. 20, 499. 10.1186/s12870-020-02700-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Sarker U., Oba S. (2019c). Protein, Dietary Fiber, Minerals, Antioxidant Pigments and Phytochemicals, and Antioxidant Activity in Selected Red Morph Amaranthus Leafy Vegetable. PLoS ONE 14, e0222517. 10.1371/journal.pone.0222517 [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Sarker U., Oba S. (2018c). Response of Nutrients, Minerals, Antioxidant Leaf Pigments, Vitamins, Polyphenol, Flavonoid and Antioxidant Activity in Selected Vegetable Amaranth under Four Soil Water Content. Food Chem. 252, 72–83. 10.1016/j.foodchem.2018.01.097 [DOI] [PubMed] [Google Scholar]
  47. Sarker U., Oba S. (2018d). Salinity Stress Enhances Color Parameters, Bioactive Leaf Pigments, Vitamins, Polyphenols, Flavonoids and Antioxidant Activity in Selected Amaranthus Leafy Vegetables. J. Sci. Food Agric. 99, 2275–2284. 10.1002/jsfa.9423 [DOI] [PubMed] [Google Scholar]
  48. Sarker U., Oba S. (2020). The Response of Salinity Stress-Induced A. Tricolor to Growth, Anatomy, Physiology, Non-enzymatic and Enzymatic Antioxidants. Front. Plant Sci. 11, 559876. 10.3389/fpls.2020.559876 [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. State Administration of Traditional Chinese Medicine. Zhong Hua Ben Cao (Shanghai: Shanghai Science and Technology Press; ), 8, 156–157. [Google Scholar]
  50. Sun J., Peng H. X., Dong X. H., Zhu E. J., Ren J. Y.HPLC Analysis Method on β-carotene in Sweet Potato. Food Sci. Techn 1, 236–238. [Google Scholar]
  51. Turan M., Kordali S., Zengin H., Dursun A., Sezen Y. (2003). Macro and Micro mineral Content of Some Wild Edible Leaves Consumed in Eastern Anatolia. Acta Agriculturae Scand. Section B - Soil Plant Sci. 53, 129–137. 10.1080/090647103100095 [DOI] [Google Scholar]
  52. Wang G. Y. (2009). Chinese Food Composition Table. 2nd Edition. Beijing: Peking University Medical Press. Available at: http://yingyang.911cha.com/M2F3.html. [Google Scholar]
  53. Wang Z. B., Gao H. Y., Wu L. J. (2010). Isolation and Identification of Chemical Constituents of Flavones from the Leaves of Acanthopanax Senticosus Harms. J. Shenyang Pharm. Univ. 27, 533–538. 10.14066/j.cnki.cn21-1349/r.2010.07.002 [DOI] [Google Scholar]
  54. Wang Z. T., Lan Z., Lu J., Jiang D. G. (2005). Introduction of GB/T 5009-2003 Methods of Food Hygienic Analysis-Physical and Chemical Section. Chin. J. Food Hyg. 17, 193–211. 10.13590/j.cjfh.2005.03.001 [DOI] [Google Scholar]
  55. Wu G. (2010). Functional Amino Acids in Growth, Reproduction, and Health. Adv. Nutr. 1, 31–37. 10.3945/an.110.1008 [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Wu X., Wang L., Wang H., Dai Y., Ye W.-C., Li Y.-L. (2012). Steroidal Saponins from Paris Polyphylla Var. Yunnanensis . Phytochemistry 81, 133–143. 10.1016/j.phytochem.2012.05.034 [DOI] [PubMed] [Google Scholar]
  57. Xing J., Li Q. L., Geng T. H., Yi H., Song S. Y. (2012). Research Development for Amino Acid Analysis and Determination. China Food Add 5, 187–191. [Google Scholar]
  58. Yang S.-L., Liu X.-K., Wu H., Wang H.-B., Qing C. (2009). Steroidal Saponins and Cytoxicity of the Wild Edible Vegetable-Smilacina Atropurpurea. Steroids 74, 7–12. 10.1016/j.steroids.2008.08.008 [DOI] [PubMed] [Google Scholar]
  59. Yang S. L. (2003). Nucleosides from Smilacina Atropurpurea . Chin. J. Nat. Med. 4, 196–198. [Google Scholar]
  60. Yokosuka A., Mimaki Y. (2008). Steroidal Glycosides from the Underground Parts of Trillium Erectum and Their Cytotoxic Activity. Phytochemistry 69, 2724–2730. 10.1016/j.phytochem.2008.08.004 [DOI] [PubMed] [Google Scholar]
  61. Zhang A. W. (2008). Advance of Research on Determination of Protein in Food. J. Farm Prod. Process. 1, 80–82. [Google Scholar]
  62. Zhang H. P., Zhang J., Liu A. J., Zhang P., Sun R. G. (2013). Analysis of Nutritional Components and Bioactive Substances of Pleurotus Eryngii . Acta Nutr. Sin. 3, 307–309. 10.13325/j.cnki.acta.nutr.sin.2013.03.002 [DOI] [Google Scholar]
  63. Zhang M. L., Guo M. H., Chen D. H. (2009). Discussion on the Methods of Moisture Determination in Different Food. Mod. Agr. Sci. Tech 21, 291–293. [Google Scholar]
  64. Zhang Y., Li H.-Z., Zhang Y.-J., Jacob M. R., Khan S. I., Li X.-C., et al. (2006). Atropurosides A-G, New Steroidal Saponins from Smilacina Atropurpurea. Steroids 71, 712–719. 10.1016/j.steroids.2006.04.005 [DOI] [PubMed] [Google Scholar]
  65. Zhao S. J., Han M., Han Z. M., Li Y. L., Yang L. M. (2009). Separation and Identification of Flavonoids from Smilacina Japonica by High Speed Counter-current Chromatography. Chin. J. Anal. Chem. 37, 1354–1358. 10.1159/000210413 [DOI] [Google Scholar]
  66. Zhao X. L., Jing W. G., Han S. Y., Sun G. L., Liu Y. M., Zhang Q. W., et al. (2011). Two New Steroidal Saponins from Dioscorea Panthaica . Phytochemistry Lett. 4, 267–270. 10.1016/j.phytol.2011.04.011 [DOI] [Google Scholar]
  67. Zhou Z. (2014). Application of Phase Coded Pulse Compression Method to Air-Coupled Ultrasonic Testing Signal Processing. Jme 50, 48–50. 10.16465/j.gste.2014.03.00410.3901/jme.2014.02.048 [DOI] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

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Data Availability Statement

The datasets presented in this article are not readily available because, All datasets had been included in the paper. Requests to access the datasets should be directed to long@mail.kib.ac.cn or long.chunlin@muc.edu.cn.

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