Effects of Steam Distillation and Screw-Pressing on Extraction,Composition and Functional Properties of Protein in Dehulled Coriander (<Emphasis Type="Italic">Coriandrum sativum</Emphasis> L.)

Coriander (Coriandrum sativum L.) is a summer annual plant commonly used as fresh green herb, spice or for its essential oil. An integrated process combined steam distillation, dehulling, and screw pressing to recover the essential oil and edible oil from coriander fruit. The current work determined the impact of the dual oil extraction approach on coriander protein extractability, composition, and functional properties and compared the results with those of ground whole coriander. Coriander protein extracts were produced by the acid precipitation method. All the dehulled samples (steamed and non‐steamed) produced protein extracts with markedly higher protein content (84–90% dry basis, db) than did ground whole fruit (67% db). Coriander protein extracts showed similar amino acid compositions and had amino acid scores that were greater than those of their starting meals and soybean protein. Steam distillation had detrimental effects on the protein, based on major changes in SDS‐PAGE band patterns and reduced protein recovery [from 42 (control) to 26%]. However, solubilities of protein from steam‐distilled samples were enhanced from pH 7 to 10 (>90 versus 80% in non‐steam‐distilled coriander). Steam‐distillation did not negatively affect foaming, emulsification, and heat coagulability properties of the coriander proteins, as the values were equal to those of the non‐steamed samples.     

Extraction of Coriander Oil Using Twin‐Screw Extrusion: Feasibility Study and Potential Press Cake Applications

This study presents an assessment of the vegetable oil extraction from coriander fruits through mechanical pressing, more specifically twin‐screw extrusion. This comprises an evaluation of the oil recovery obtained and its respective quality, as well as the specific mechanical energy, representing an economical point of view. With regard to the extrusion optimization, the screw configuration, the device's filling coefficient and the pressing temperature were varied. The screw configuration was shown to exhibit a key influence on the extraction efficiency and oil recoveries of at least 40 % were reached when the pressing zone was positioned immediately after the filter and consisted of 50 mm long, reverse screws with a ‐33 mm pitch. Furthermore, with a device's filling coefficient of 39.4 g/h rpm and a pressing temperature of 120 °C, an oil recovery of 47 %, the highest of this study, was reached with concurrent low energy consumption. Next to this, operating parameters of 47.1 g/h rpm and 80 °C resulted in the production of a press cake with the lowest residual oil content (15 %) in this study, although this also involved a significant increase in the filtrate's foot content. All the produced oils were of acceptable quality (<1.5 % acidity), showed high petroselinic acid content (73 %), and were pleasantly scented.     

Composition, Structure and Functional Properties of Protein Concentrates and Isolates Produced from Walnut (Juglans regia L.)

In this study, composition, structure and the functional properties of protein concentrate (WPC) and protein isolate (WPI) produced from defatted walnut flour (DFWF) were investigated. The results showed that the composition and structure of walnut protein concentrate (WPC) and walnut protein isolate (WPI) were significantly different. The molecular weight distribution of WPI was uniform and the protein composition of DFWF and WPC was complex with the protein aggregation. H(0) of WPC was significantly higher (p < 0.05) than those of DFWF and WPI, whilst WPI had a higher H(0) compared to DFWF. The secondary structure of WPI was similar to WPC. WPI showed big flaky plate like structures; whereas WPC appeared as a small flaky and more compact structure. The most functional properties of WPI were better than WPC. In comparing most functional properties of WPI and WPC with soybean protein concentrate and isolate, WPI and WPC showed higher fat absorption capacity (FAC). Emulsifying properties and foam properties of WPC and WPI in alkaline pH were comparable with that of soybean protein concentrate and isolate. Walnut protein concentrates and isolates can be considered as potential functional food ingredients.     

Impact of extraction conditions and seed variety on the characteristics of pennycress (Thlaspi arvense) protein: a structure and function approach

As the consumer demand for plant proteins continues to grow, the food industry is seeking novel and sustainable protein sources to incorporate in various food products. Pennycress (Thlaspi arvense), a sustainable cover crop, produces oilseeds high in protein, warranting investigation. Accordingly, protein extraction from pennycress was evaluated under various extraction conditions, using alkaline extraction and salt solubilization coupled with ultrafiltration. Given the superior color and functionality of the salt extracted pennycress protein isolate (PcPI), its production was scaled-up about two hundred folds in a pilot plant. Furthermore, a new pennycress accession bred to have zero erucic acid (0EA) was evaluated to determine the impact of seed variety on protein characteristics. Structural and functional characterization was performed on PcPI and compared to native (nSPI) and commercial (cSPI) soy protein isolates. Salt extracted PcPI had comparable gel strength to cSPI, three times higher solubility under acidic conditions, and ~1.5 times better emulsification capacity. PcPI extracted from 0EA was mildly different in structure and functionality from that extracted from wildtype pennycress, with the slight variation attributed to genetic variance. Finally, the protein digestibility-corrected amino acid score (PDCAAS) of the salt extracted PcPI, calculated in vivo (0.72) and in vitro (0.87), was superior or comparable to other plant protein sources. This research provided, for the first time, a comprehensive evaluation of different protein extraction protocols to produce a functional PcPI that can compete with soy protein for various food applications, such as acidic beverages, meat and dairy products, and emulsified systems.     

Properties of Soy Protein Produced by Countercurrent,Two-Stage,Enzyme-Assisted Aqueous Extraction

Enzyme-assisted aqueous extraction processing (EAEP) is an environmentally friendly technology where oil and protein can be simultaneously extracted from soybeans by using water and protease. Countercurrent, two-stage, EAEP was performed at a 1:6 solids-to-liquid ratio, 50 °C, pH 9.0, and 120 rpm for 1 h to extract oil and protein from soybeans. The skim fractions were produced by three methods: (1) by treating with 0.5 % protease (wt/g extruded flakes) in both extraction stages; (2) by treating with 0.5 % protease in the 2nd extraction stage only; and (3) by using the same two-stage extraction procedure without enzymes in either extraction stages. Countercurrent, two-stage, protein extraction of air-desolventized, hexane-defatted, soybean flakes was used as a control. Solubility profiles of the skim proteins were the typical U-shaped curves with the lowest solubility at the isoelectric point of soy protein (pH 4.5). The use of the enzyme slightly improved solubility of the recovered protein with hydrolyzed proteins having higher solubilities at acid pH. Emulsification and foaming properties were generally reduced by the use of enzyme during EAEP extractions. The skims produced with protease-extracted (hydrolyzed) proteins gave gels with lower hardness than did unhydrolyzed proteins when heated at 80 °C. The essential amino acid compositions and protein digestibilities were not adversely affected by either extrusion or extraction treatments.     

Functional Properties of Protein Isolates Produced by Aqueous Extraction of De-hulled Yellow Mustard

Two types of protein isolates were prepared from de‐hulled yellow mustard flour by aqueous extraction, membrane processing and isoelectric precipitation. The precipitated and soluble protein isolates had 96.0 and 83.5% protein content on a moisture and oil free basis, respectively. Their functional properties were evaluated and compared with commercial soybean and other Brassica protein isolates. The soluble protein isolate exhibited high values for all properties. The precipitated protein isolate showed excellent oil absorption and emulsifying properties but poor solubility, water absorption and foaming properties due to its high lipid content (~25%). Storage temperature had limited effect on lipid oxidation, and hence the stability of the precipitated protein isolate at 25–45 °C. Flavor of wieners and bologna prepared with 2% of this isolate as binder was comparable to those prepared with soy protein isolate.     

Kinetics and Thermodynamics of Oil Extraction from Olive Cake

The kinetics of oil extraction from olive cake by using ethanol 96% was studied for different solvent-to-solids ratios and temperatures. The thermodynamic aspect of the extraction process was also examined. In the kinetic study, the results produced by the model of So and Macdonald (a model involving two main mechanisms of oil extraction: a washing process and a diffusion process with two stages) were found to be in good agreement with the experimental data. The yield of oil in the extract increased with increasing contact time, solvent-to-solids ratio and extraction temperature. The calculated values of the mass transfer coefficients of various stages of the extraction were found to increase linearly with solvent-to-solids ratio and temperature. In all cases, the predominant mechanism in the extraction was the washing of the oil occurring on the particle surface. The values of the activation energy were 8.56 kJ mol⁻¹ for the washing stage, 9.88 kJ mol⁻¹ for the first stage of diffusion and 17.55 kJ mol⁻¹ for the second stage of diffusion by changing temperature from 20 to 50 °C. Further, the results obtained from thermodynamic study of extraction process gave positive values of enthalpy and entropy changes and negative values of change in free energy. Under the equilibrium conditions, the temperature coefficient was found to be 1.02.     

Antioxidant Activity of Sesame (Sesamum indicum L.) Cake Extract for the Stabilization of Olein Based Butter

This study investigated the effect of ethanolic sesame cake extract on oxidative stabilization of olein based butter. Fractionation of cream was performed by the dry fractionation technique at 10 °C, ethanolic sesame cake extract (SCE) was incorporated into olein butter at three different concentrations; 50, 100, 150 ppm (T₁, T₂, T₃) and compared with a control. The total phenolic content of SCE was 1.72 (mg gallic acid equivalent g^?1 dry weight). The HPLC characterization of ethanolic sesame cake revealed the presence of antioxidant substances viz. sesamol, sesamin and sesamolin in higher extents. The DPPH free radical scavenging activity of SCE was 83 % as compared to 64 and 75 % in BHA and BHT. Fractionation of milk fat at 10 °C significantly (p < 0.05) influenced the fatty acid profile of olein and stearin fractions from the parent milk fat. Concentration of oleic acid and linoleic acid in olein fraction was 29.62 and 33.46 % greater than the parent milk fat. The loss of C18:1 in 90 days stored control and T₃ was 24.37 and 3.58 %, respectively, 58 % C18:2 was broken down into oxidation products over 8.55 % loss in T₃. The peroxide value of control, T₁, T₂, BHT and T₃ in the Schaal oven test was 8.59, 8.12, 5.34, 4.52 and 2.49 (mequiv O₂/kg). The peroxide value and anisidine value of 3 months stored control and T₃ were 1.21, 0.42 (mequiv O₂/kg) and 27.25, 13.25, respectively. The concentration of conjugated dienes in T₃ was substantially less than the control. The induction period of T₃ was considerably higher than BHT with no difference in sensory characteristics (p > 0.05). Ethanolic SCE can be used for the long‐term preservation of olein butter, with acceptable sensory characteristics.     

Antioxidative and Functional Properties of Pumpkin Oil Cake Globulin Hydrolysates

Cucurbitin extracted from pumpkin (Cucurbita pepo) oil cake was enzymatically hydrolysed with three different enzymes viz. alcalase, flavourzyme and pepsin. Antioxidative and functional properties of cucurbitin hydrolysates with different degrees of hydrolysis (DH) were investigated. The antioxidant activity of the hydrolysates was strongly dependent on the enzyme used. The hydrolysates obtained by alcalase and pepsin showed antioxidative potential whereas flavourzyme hydrolysates did not demonstrate these activities. Reducing power and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) scavenging activity of cucurbitin hydrolysate were positively related to DH. The highest antioxidant activity was found in the hydrolysate obtained by alcalase at DH 25.6 % [reducing power of 0.25 ± 0.01 A700 nm and ABTS scavenging activity of 3.34 ± 0.02 mmol/L Trolox equivalent antioxidant coefficients (TEAC)]. Hydrolysis by all enzymes increased the protein solubility within the studied pH range. The best emulsion activity and stability index (EAI = 143.28 ± 3.05 m²/g and ESI = 87.5 ± 1.96 min) have hydrolysates produced by flavourzyme (DH 9.2 %) whereas alcalase produced hydrolysates with the best foaming capacity (FC = 242 ± 3.21). The results demonstrate that hydrolysates produced in the present study have good functional properties as well as antioxidant activity indicating their possible use in different food systems.     

Functional Properties of Soy Protein Isolates Prepared from Gas-Supported Screw-Pressed Soybean Meal

White flakes (WFs) are obtained from dehulled flaked soybeans by extracting oil with hexane and flash- or downdraft-desolventizing the (defatted) flakes, and WFs are the normal feedstock used to produce soy protein ingredients. Gas-supported screw pressing (GSSP) is a new oilseed crushing technology in which traditional screw pressing is combined with injecting high-pressure CO₂, thereby producing hexane-free, low-fat, high-PDI soybean meal. The objectives of the present study were to evaluate yields, compositions, and functional properties of soy protein isolates (SPIs) produced from GSSP soybean meal and to compare these properties to those of SPIs produced from WFs. GSSP meals produced SPIs in significantly higher yields (59.7–63.1% vs. 51.6–61.1%), with greater free (0.05–0.40%) and bound fat (3.70–4.92%) contents than did WFs. There were no significant differences in protein contents of the SPI; all exceeded 90% protein content (db). SPIs prepared from GSSP meals had similar or slightly lower water-solubilities compared to SPIs prepared from WFs. SPIs prepared from GSSP meals had higher water-holding capacities and viscosities, and significantly better emulsifying and fat-binding properties compared to SPIs prepared from WFs. SPIs prepared from WFs had significantly better foaming properties compared to SPIs prepared from GSSP meals, which were attributed to the lower fat contents of SPIs prepared from WFs.     

Physicochemical Properties and ACE-I Inhibitory Activity of Protein Hydrolysates from a Non-Genetically Modified Soy Cultivar

Arkansas‐grown non‐genetically modified soybean cultivar, R08‐4004, was selected to prepare a protein isolate, which was treated with Alcalase for limited enzymatic hydrolysis. The objective was to optimize the Alcalase hydrolysis condition to produce soy protein hydrolysate (SPH) with high protein yield, low bitterness, and clarity for beverage applications. The degree of hydrolysis ranged between 14 and 52 % during the study at varying incubation times using two different concentrations of Alcalase enzyme. Recovery of soluble protein, between 21 and 53 %, was achieved with a decrease in turbidity. There was an increase in surface hydrophobicity (S₀) which is correlated with bitterness of SPH treated with 1.0 AU (3.2 µL/g) of Alcalase 2.4 L. The sodium dodecyl sulfate‐polyacrylamide gel electrophoresis analysis showed a distinct hydrolysis pattern in which 7S globulin and the two acidic sub‐units of 11S globulin were hydrolyzed extensively in comparison to the two basic sub‐units of 11S globulin. Limited enzymatic hydrolysis produced low molecular weight peptides <17 kDa. Among these SPHs, the one derived after 120 min incubation had the highest soluble protein yield (43 %), low S₀ value (35.4), low turbidity (0.88), and highest angiotensin‐I converting enzyme (ACE‐I) inhibition activity (66.6 %). This hydrolysate has potential use as protein rich nutraceutical for developing many non‐genetically modified food product applications.     

Amino Acid Composition,Molecular Weight Distribution and Gel Electrophoresis of Walnut (Juglans regia L.) Proteins and Protein Fractionations

As a by-product of oil production, walnut proteins are considered as an additional source of plant protein for human food. To make full use of the protein resource, a comprehensive understanding of composition and characteristics of walnut proteins are required. Walnut proteins have been fractionated and characterized in this study. Amino acid composition, molecular weight distribution and gel electrophoresis of walnut proteins and protein fractionations were analyzed. The proteins were sequentially separated into four fractions according to their solubility. Glutelin was the main component of the protein extract. The content of glutelin, albumin, globulin and prolamin was about 72.06%, 7.54%, 15.67% and 4.73% respectively. Glutelin, albumin and globulin have a balanced content of essential amino acids, except for methionine, with respect to the FAO pattern recommended for adults. SDS-PAGE patterns of albumin, globulin and glutelin showed several polypeptides with molecular weights 14.4 to 66.2 kDa. The pattern of walnut proteins in two-dimension electrophoresis (2-DE) showed that the isoelectric point was mainly in the range of 4.8–6.8. The results of size exclusion chromatogram indicated molecular weight of the major components of walnut proteins were between 3.54 and 81.76 kDa.     

Argan (Argania spinosa L.) Seed Oil Cake as a Potential Source of Protein-Based Film Matrix for Pharmaco-Cosmetic Applications

Various different agri-food biomasses might be turned into renewable sources for producing biodegradable and edible plastics, potentially attractive for food, agricultural and cosmeceutical sectors. In this regard, different seeds utilized for edible and non-edible oil extraction give rise to high amounts of organic by-products, known as seed oil cakes (SOCs), potentially able to become protein-rich resources useful for the manufacturing of biodegradable films. This study reports the potential of SOC derived from Argania spinosa (argan), a well-known plant containing valuable non-refined oil suitable for food or cosmetic use, to be a promising valuable source for production of a protein-based matrix of biomaterials to be used in the pharmaco-cosmetic sector. Thus, glycerol-plasticized films were prepared by casting and drying using different amounts of argan seed protein concentrate, in the presence of increasing glycerol concentrations, and characterized for their morphological, mechanical, barrier, and hydrophilicity properties. In addition, their antioxidant activity and effects on cell viability and wound healing were investigated. The hydrophobic nature of the argan protein-based films, and their satisfying physicochemical and biological properties, suggest a biorefinery approach for the recycling of argan SOC as valuable raw material for manufacturing new products to be used in the cosmeceutical and food industries.     

Toxic Compound,Anti-Nutritional Factors and Functional Properties of Protein Isolated from Detoxified Jatropha curcas Seed Cake

Jatropha curcas is a multipurpose tree, which has potential as an alternative source for biodiesel. All of its parts can also be used for human food, animal feed, fertilizer, fuel and traditional medicine. J. curcas seed cake is a low-value by-product obtained from biodiesel production. The seed cake, however, has a high amount of protein, with the presence of a main toxic compound: phorbol esters as well as anti-nutritional factors: trypsin inhibitors, phytic acid, lectin and saponin. The objective of this work was to detoxify J. curcas seed cake and study the toxin, anti-nutritional factors and also functional properties of the protein isolated from the detoxified seed cake. The yield of protein isolate was approximately 70.9%. The protein isolate was obtained without a detectable level of phorbol esters. The solubility of the protein isolate was maximal at pH 12.0 and minimal at pH 4.0. The water and oil binding capacities of the protein isolate were 1.76 g water/g protein and 1.07 mL oil/g protein, respectively. The foam capacity and stability, including emulsion activity and stability of protein isolate, had higher values in a range of basic pHs, while foam and emulsion stabilities decreased with increasing time. The results suggest that the detoxified J. curcas seed cake has potential to be exploited as a novel source of functional protein for food applications.     

Toxic Compound, Anti-Nutritional Factors and Functional Properties of Protein Isolated from Detoxified Jatropha curcas Seed Cake

Jatropha curcas is a multipurpose tree, which has potential as an alternative source for biodiesel. All of its parts can also be used for human food, animal feed, fertilizer, fuel and traditional medicine. J. curcas seed cake is a low-value by-product obtained from biodiesel production. The seed cake, however, has a high amount of protein, with the presence of a main toxic compound: phorbol esters as well as anti-nutritional factors: trypsin inhibitors, phytic acid, lectin and saponin. The objective of this work was to detoxify J. curcas seed cake and study the toxin, anti-nutritional factors and also functional properties of the protein isolated from the detoxified seed cake. The yield of protein isolate was approximately 70.9%. The protein isolate was obtained without a detectable level of phorbol esters. The solubility of the protein isolate was maximal at pH 12.0 and minimal at pH 4.0. The water and oil binding capacities of the protein isolate were 1.76 g water/g protein and 1.07 mL oil/g protein, respectively. The foam capacity and stability, including emulsion activity and stability of protein isolate, had higher values in a range of basic pHs, while foam and emulsion stabilities decreased with increasing time. The results suggest that the detoxified J. curcas seed cake has potential to be exploited as a novel source of functional protein for food applications.     

Tannery Waste Treatment: Leaching,Filtration and Cake Dewatering Using a Membrane Filter Press (a Pilot Plant Study)

Abstract

In Alcanena (Portugal) the waste water treatment plant (WWTP) receives tannery waste, after a pretreatment for sulphides and the tanning exhaust baths have been sent to a recovery unit and the municipal waste water from Alcanena residential area. Physical, chemical, and biological treatment processes are involved, and the end products are sludge of ～71% moisture containing mainly organic matter, sulfides, iron, chromium, and other metals. The sludge is dumped, after stabilization, in a specially designed hazardous waste landfill.

In this study, tannery mixed sludge (from chemical and biological treatments) was leached and filtered. Leaching was carried out using sulfuric acid (pH 0.5) to release residual sulfides and metals from the slurry. Hydrogen sulfide (H₂S) was flushed out into an oxidation trap (hypochlorite/alkaline tank) in which H₂S transforms to soluble sulfate. The acidified sludge was fed into a membrane filter press where it was filtered, acid‐washed, water–washed, membrane‐squeezed, and vacuum‐dried reaching lower moisture levels (20–30%). The process cycle is approximately 101–137 min in our experiments; however, from this work, a cycle of 90 min to produce cakes with 0.9 cm thickness in the industrial scale through cutting some operational time, reaching final moisture of ～20% at the end of the dewatering cycle, can be estimated. Filtration was carried out at different feed pressure (3–5 bar) with and without diatomite precoating. The effect of different amounts of diatomite body‐feed was studied. Specific cake resistance, α, was found to increase with the increase in feed pressure and to decrease with diatomite precoating and the increased amounts of diatomite body feed. Cake washing was accomplished using 0.05 M H₂SO₄ (acid washing), to remove residual metals, followed by water washing, to remove cake acidity. Cake dewatering via membrane squeezing was applied using hot water (65°C), and cake moisture was dropped from ～71% before squeezing to 42% after squeezing. With vacuum application over the hot cakes, for 30 min, cake moisture decreased to ～20% for cakes with an average thickness of 0.9 cm. Cake chemical analysis showed chromium levels lower than 1000 mg/kg (the maximum Cr concentration allowed by the Portuguese legislation in a solid residue for use in agricultural soil). In addition, produced cake (without diatomite body feed) has a calorific value of 11,000 kJ/kg and accordingly it can be used as a source of energy.     

东方蓼提取物杀虫杀菌活性初探

东方蓼阴干样品经初步粉碎后,分别用体积比为1∶6的乙醇-石油醚和乙酸乙酯浸泡提取,将提取物稀释至4000mg/L后,分别对黏虫、淡色库蚊、小菜蛾、桃蚜、朱砂叶螨;小麦白粉病、黄瓜霜霉病、黄瓜炭疽病进行室内生物活性测定试验,结果表明,东方蓼茎石油醚提取物具有较强的杀虫杀菌活性,对淡色库蚊、黏虫和桃蚜的杀虫效果分别可达90%、80%和80%,对黄瓜霜霉病的杀菌效果可达80%,对小麦白粉病的杀菌效果可达40%。     

Microwave-Assisted Extraction and Solid-Phase Separation of Quercetin from Solid Onion (Allium cepa L.)

The challenge of extraction of natural product in the twenty-first century is to achieve 100% selectivity of the desired product and develop renewable energy based processes. An object of the present work is to provide a method for producing specific bioactive compounds from agricultural products. A simple protocol was used to obtain the conditions of microwave-assisted extraction (MWAE) and ultrasound-assisted extraction (USAE). Total quercetin content under microwave irradiation for 150 sec at pH 6.25 (209 mg/ 100 gm F. wt). The effects of operating conditions, such as extraction time and pH on the extraction yield of quercetin were studied. Microwave-assisted ionic liquid-based silica sorbent (ILSis) was developed by a process involving surface chemical modification of commercial silica using a synthesized ionic liquid and characterized by FTIR. The obtained particles were successfully used as a special sorbent in a solid-phase separation process to isolate quercetin and its glycosides from solid onion. Different washing and elution solvents, such as water, water/methanol (v/v), and pure methanol were evaluated. Ionic liquid-based silica sorbent was compared with traditional C18 sorbent and it exhibited higher selectivity. The target compounds in solid onion containing quercetin and its glycosides were determined.     

岗稔果色素的提取及性状研究

以００５ｍｏｌ／ＬＨＣｌ－４０％乙醇溶液为浸提剂,４０℃浸提８ｈ（由ＳＡＳ软件统计分析确定）,岗稔色素的提取率达７８％。同时,对色素吸收光谱,薄层色谱及其耐光、耐热、耐氧化及还原稳定性进行了研究。初步确定色素组成为花癸素 ３,５ 二葡萄糖苷,矢车菊 ３ 半乳糖苷,飞燕草 ３ 半乳糖苷。     

正交设计法优化丝瓜总皂苷的提取工艺

对丝瓜总皂苷的最佳提取工艺进行了研究。以香草醛-冰醋酸法测得的总皂苷含量为依据,利用正交设计确定了提取剂、提取时间、固液比和pH值等提取工艺参数。结果表明,丝瓜总皂苷的最佳提取剂为70%乙醇作提取剂;提取时间为2h;固液比为1/30(g/mL);pH值为7.0,此时产量为每50g丝瓜中含总皂苷约0.162g,用于工业化生产可提高丝瓜总皂苷的产量。