Scientia Agricultura Sinica ›› 2026, Vol. 59 ›› Issue (17): 3871-3889.doi: 10.3864/j.issn.0578-1752.2026.17.012

• FOOD SCIENCE AND ENGINEERING • Previous Articles     Next Articles

Exploration of Processing Applications Based on Differences in the Composition and Functional Properties of Lentinula edodes Polyphenol Extracts

BAO RuoTong(), MA GaoXing(), HU QiuHui, ZHAO XinYi, ZHANG Ran, LI CaoYu, LI WenQi, GUO WenLuo   

  1. College of Food Science and Engineering, Nanjing University of Finance and Economics/Jiangsu Province Engineering Research Center of Edible Fungus Preservation and Intensive Processing/Collaborative Innovation Center for Modern Grain Circulation and Safety, Nanjing 210023
  • Received:2026-01-24 Accepted:2026-04-13 Online:2026-09-03 Published:2026-09-03
  • Contact: MA GaoXing

Abstract:

【Objective】To address industry challenges, such as low added value and poor processability of deep-processed Lentinula edodes products caused by regional variations, the major cultivar ‘Shenxiang 1513’ from two primary production regions in China, including Qingyuan (Zhejiang) and Suizhou (Hubei), was selected as research object. Based on the unique occurrence forms and health benefits of L. edodes polyphenols, this study systematically compared the composition and functional properties of polyphenol extracts obtained using different extraction methods. The goal was to identify their potential processing and application directions for these extracts (LEPs), and to provide a theoretical basis for the targeted development of high-value-added L. edodes products.【Method】LEPs were prepared using three techniques: hot water extraction (H), microwave-assisted extraction (M), and ultrasonic-assisted extraction (U). Their microstructure and chemical composition were analyzed using scanning electron microscopy (SEM) and liquid chromatography-mass spectrometry (LC-MS), respectively, along with analysis of their physicochemical properties. In vitro antioxidant capacity was evaluated through radical scavenging and reducing power assays. Hypoglycemic and hypolipidemic potential were assessed by measuring inhibition of major digestive enzymes, intrinsic fluorescence quenching, and glycolipid adsorption capacity, enabling a multidimensional quality evaluation of LEPs.【Result】The total polyphenol content of LEPs ranged from 2.82 to 5.51 mg GAE·g-1, and total flavonoid content ranged from 5.69 to 6.81 mg RE·g-1. LC-MS analysis showed that the polyphenol extract from Qingyuan contained higher levels of rutin, benzoic acid, 3,4-dihydroxybenzoic acid, and 4-hydroxybenzoic acid, whereas the polyphenol extract from Suizhou was mainly composed of 3,4-dihydroxybenzoic acid, vanillic acid, and benzoic acid. Basic physicochemical characterization indicated that LEPs had good solubility and oil-holding capacity. In antioxidant assays, Qingyuan-H exhibited the strongest scavenging capacity against ABTS+ radicals and hydroxyl radicals, with IC50 (half-maximal inhibitory concentration) values of 0.18 and 3.25 mg·mL-1, respectively. Qingyuan-M showed higher activity in DPPH radical scavenging and reducing power, with a half-inhibitory concentration of 1.49 mg·mL-1 for DPPH, and a reducing power of 5.20 mg AAE·(g DW) -1 at 6 mg·mL-1. In vitro hypoglycemic assays confirmed that L. edodes polyphenol extracted from Qingyuan had a stronger glucose-lowering effect than that from Suizhou. The IC50 of Qingyuan-M against α-glucosidase was 1.63 mg·mL-1, and the fluorescence quenching mechanism was determined to be static quenching. Its glucose-binding capacity was 211.64 µmol·g-1. The polyphenol extract from Suizhou showed higher pancreatic lipase inhibition than that from Qingyuan. Suizhou-M achieved 66.63% inhibition, with binding rates of 28.93% and 48.74% for sodium glycocholate and sodium taurocholate, respectively.【Conclusion】This study indicated that regional differences influenced the functional properties of L. edodes polyphenols and could guide processing strategies. Qingyuan sources mushrooms were more suitable for targeted development of natural antioxidant products. Polyphenols extracted from Qingyuan L. edodes via microwave-assisted extraction (Qingyuan-M) demonstrated outstanding glucose-lowering efficacy and were promising raw materials for hypoglycemic functional products. In contrast, polyphenols extracted from Suizhou L. edodes using the same method were more suitable for lipid-lowering product development.

Key words: Lentinula edodes polyphenol, composition, physicochemical properties, functional characteristics, processing direction

Table 1

Information of Lentinula edodes samples"

试验材料Material 庆元香菇 L. edodes, Qingyuan 随州香菇 L. edodes, Suizhou
供货商Supplier 浙江香满亭生物科技有限公司
Zhejiang xiangmanting Biotechnology Co., Ltd
湖北长久菌业有限公司
Hubei Changjiu Fungi Industry Co., Ltd
采摘地点Collection site 浙江省庆元县香菇生产基地
L. edodes Production Base, Qingyuan County, Zhejiang Province
湖北省随州市香菇生产基地
L. edodes Production Base, Suizhou City, Hubei Province
品种Variety 申香1513 Shenxiang1513
采摘时间Harvest date 2023年冬季;同一潮次Winter 2023, Same flush
购买时间Purchase date 2024年3月 March 2024
干制条件Drying conditions 50—65 ℃烘干24 h Dried at 50-65 ℃ for 24 h

Fig. 1

Scanning electron micrographs of LEPs H: Hot water extraction; M: Microwave-assisted extraction; C: Ultrasonic-assisted extraction. The same as below"

Table 2

Comparative analysis of the total phenolic and flavonoid content in LEPs"

样品
Sample
总多酚含量
Total phenolic content
(mg GAE·g-1)
总黄酮含量
Total flavonoid content
(mg RE·g-1)
庆元-H Qingyuan-H 5.19±0.03b 6.78±0.04a
庆元-M Qingyuan-M 5.51±0.09a 6.81±0.08a
庆元-U Qingyuan-U 4.28±0.02c 6.25±0.08b
随州-H Suizhou-H 2.82±0.08f 5.69±0.02e
随州-M Suizhou-M 3.30±0.06d 5.98±0.08c
随州-U Suizhou-U 2.94±0.07e 5.83±0.04d

Table 3

Quantitative analysis of the main components in LEPs (μg·g-1)"

酚类化合物
Phenolic compound
样品 Sample
庆元-H
Qingyuan-H
庆元-M
Qingyuan-M
庆元-U
Qingyuan-U
随州-H
Suizhou-H
随州-M
Suizhou-M
随州-U
Suizhou-U
原儿茶酸 3,4-Dihydroxybenzoic 2.7612±0.0357b 3.3492±0.0760a 2.7500±0.1000b
4-羟基苯甲酸 4-Hydroxybenzoic acid 3.4462±0.0783b 3.3937±0.0427b 3.5674±0.1156b 8.2075±0.2961a 8.0888±0.3377a 7.9664±0.2693a
香草酸 Vanillic acid 1.9755±0.1153a 1.8067±0.04451b 1.6457±0.0760c
咖啡酸 Caffeic acid 0.2747±0.0058a 0.2563±0.0023b 0.2529±0.0108b 0.1820±0.0055c 0.1623±0.0058d 0.1537±0.0100d
丁香酸 Syringic acid 0.1454±0.0039d 0.1416±0.0025d 0.1143±0.0022d 0.8325±0.0426a 0.7087±0.0200b 0.6374±0.0379c
香草醛 Vanillin 0.0509±0.0013c 0.0493±0.0009c 0.0408±0.0023d 0.2053±0.0061a 0.1473±0.0037b 0.1539±0.0095b
丁香醛 Syringaldehyde 0.0929±0.0051a 0.0627±0.0033c 0.0762±0.0030b
芦丁 Rutin 7.3605±0.1846a 7.4744±0.0510a 6.8880±0.0509b 0.2932±0.0062c 0.3025±0.0198c 0.2917±0.0108c
牡荆素 Vitexin 0.1013±0.0019d 0.1069±0.0012d 0.0505±0.0013e 0.2998±0.0170a 0.1808±0.0092b 0.1293±0.0048c
反式阿魏酸 Trans-Ferulic acid 0.0745±0.0004c 0.0832±0.0017b 0.1674±0.0023a 0.0361±0.0010e 0.0604±0.0023d 0.0615±0.0034d
槲皮素-3-O-葡萄糖苷 Quercetin 3-β-D-glucoside 0.7544±0.0196a 0.7444±0.0261a 0.6699±0.0437b 0.0668±0.0016c 0.0579±0.0017c 0.0390±0.0023c
二氢槲皮素 (+)-Dihydroquercetin 0.1812±0.0043a 0.1740±0.0035b 0.1846±0.0036a
苯甲酸 Benzoic acid 3.2042±0.2478b 3.9258±0.1279a 2.9956±0.1834b 1.6012±0.0876c 1.3856±0.0513c 1.4241±0.0931c
山奈酚-3-O-葡萄糖苷 Kaempferol-3-O-glucoside 0.1345±0.0015b 0.1380±0.001a 0.1185±0.0016c 0.0367±0.0015d 0.0319±0.0019e 0.0294±0.0031e
二氢山奈酚 (+)-Dihydrokaempferol 0.0340±0.0007a 0.0288±0.0004c 0.0322±0.0017b
白藜芦醇 Resveratrol 0.0024±0.0003a 0.0012±0.0003b
槲皮素 Quercetin 0.1393±0.0032b 0.1355±0.0014c 0.1493±0.0040a 0.0153±0.0012d 0.0119±0.0004d 0.0135±0.0011d
氢化肉桂酸 Hydrocinnamic acid 0.4226±0.0079b 0.4558±0.0138a 0.4307±0.0119ab 0.2342±0.0214c 0.2185±0.0106c 0.2181±0.0226c
反式肉桂酸 Trans-Cinnamic acid 1.0034±0.0051a 0.9861±0.0032a 0.9551±0.0231b 0.2228±0.0094d 0.2479±0.0100c 0.2212±0.0140d
柚皮素 Naringenin 0.0044±0.0003a 0.0044±0.0003a 0.0026±0.0003b
山奈酚 Kaempferol 0.011±0.0004a 0.0081±0.0003c 0.0092±0.0002b

Table 4

The water solubility, water and oil holding capability of LEPs"

样品
Sample
溶解性
Water solubility (%)
持水力
Water-holding capacity (g·g-1)
持油力
Oil-holding capacity (g·g-1)
庆元-H Qingyuan-H 85.99±4.66a 0.07±0.03d 2.02±0.03b
庆元-M Qingyuan-M 87.90±5.29a 0.26±0.01c 2.19±0.03ab
庆元-U Qingyuan-U 89.35±2.10a 0.06±0.02d 2.13±0.02ab
随州-H Suizhou-H 89.61±4.72a 0.56±0.08b 1.98±0.14b
随州-M Suizhou-M 86.41±5.45a 0.76±0.15a 2.34±0.24a
随州-U Suizhou-U 86.33±3.47a 0.34±0.16c 1.93±0.21b

Fig. 2

Antioxidant activity of LEPs in vitro Different lowercase letters indicate significant difference among different samples at the same concentration (P<0.05). The same as below"

Table 5

Antioxidant capacity analysis of LEPs"

样品
Sample
半抑制浓度IC50 (mg·mL-1) 抗坏血酸当量 AAE (mg AAE·g-1 DW)
DPPH· ABTS+· ·OH 还原力 Reducing power
庆元-H Qingyuan-H 1.73±0.22d 0.18±0.01d 3.25±0.12c 5.00±0.07d
庆元-M Qingyuan-M 1.49±0.08e 0.21±0.01c 3.45±0.06c 5.20±0.08e
庆元-U Qingyuan-U 1.61±0.05de 0.21±0.00c 3.38±0.16c 4.99±0.04d
随州-H Suizhou-H 3.27±0.07b 0.31±0.01b 6.48±0.31b 2.94±0.03a
随州-M Suizhou-M 2.59±0.11c 0.35±0.01a 7.79±0.51a 3.10±0.05c
随州-U Suizhou-U 3.64±0.11a 0.35±0.01a 8.07±0.54a 3.01±0.03b

Fig. 3

Inhibitory effect of LEPs on α-glucosidase activity"

Table 6

IC50 of LEPs against α-glucosidase"

庆元-H
Qingyuan-H
庆元-M
Qingyuan-M
庆元-U
Qingyuan-U
随州-H
Suizhou-H
随州-M
Suizhou-M
随州-U
Suizhou-U
半抑制浓度IC50 (mg·mL-1) 2.62±0.19b 1.63±0.09a 1.70±0.03a 2.87±0.20c 2.65±0.04b 2.85±0.11c

Fig. 4

Effects of LEPs on α-glucosidase fluorescence spectra A: Qingyuan-H; B: Qingyuan-M; C: Qingyuan-U; D: Suizhou-H; E: Suizhou-M; F: Suizhou-U"

Fig. 5

Stern-Volmer curve (A), lg plot (B) of LEPs pairs for α-glucosidase"

Table 7

Parameters of LEPs’ interaction with α-Glucosidase"

Stern-Volmer方程R2 Ka (mL·mg-1) n
庆元-H Qingyuan-H 0.9966 0.2021 0.87
庆元-M Qingyuan-M 0.9970 0.3768 0.40
庆元-U Qingyuan-U 0.9682 0.3089 0.48
随州-H Suizhou-H 0.9593 0.0296 2.46
随州-M Suizhou-M 0.9985 0.1222 1.34
随州-U Suizhou-U 0.9924 0.1357 0.90

Fig. 6

Glucose adsorption capacity of LEPs"

Fig. 7

Inhibitory effect of LEPs on pancreatic lipase activity"

Fig. 8

Effects of LEPs on pancreatic lipase fluorescence spectra A: Qingyuan-H; B: Qingyuan-M; C: Qingyuan-U; D: Suizhou-H; E: Suizhou-M; F: Suizhou-U"

Fig. 9

Stern-Volmer curve (A), lg plot (B) of LEPs pairs for pancreatic lipase"

Table 8

Parameters of LEPs' interaction with pancreatic lipase"

Stern-Volmer方程R2 Ka (mL·mg-1) n
庆元-H Qingyuan-H 0.9933 0.6051 0.5525
庆元-M Qingyuan-M 0.9965 0.5585 0.8104
庆元-U Qingyuan-U 0.9963 0.5470 0.6062
随州-H Suizhou-H 0.9773 0.8473 0.3218
随州-M Suizhou-M 0.9988 1.0083 0.5266
随州-U Suizhou-U 0.9980 0.8838 0.4966

Fig. 10

Binding capacity of LEPs to sodium glycocholate (A), and binding capacity of LEPs to sodium taurocholate (B)"

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