杏鲍菇黄酮提取工艺的优化

研究了利用超声波辅助复合酶法提取杏鲍菇黄酮的最优条件。在单因素试验的基础上,固定其他影响因素,选择料液比、超声时间、酶解温度和酶解pH进行四因素三水平的正交试验。结果表明：料液比为1∶50 （g/mL）、超声时间为6 min、酶解温度为50℃、酶解pH为54的条件下,获得的黄酮提取率最高,可达3352%。     

酶辅助法提取透骨草中总黄酮及抗氧化性研究

本文采用纤维素酶辅助法提取透骨草中总黄酮,即先用纤维素酶酶解透骨草,再用乙醇回流法提取透骨草中的总黄酮。分别固定提取剂乙醇浓度为70%,料液比为1∶20 g/m L,初步探究了纤维素酶浓度、酶解p H、酶解温度、酶解时间四个单因素对透骨草总黄酮提取率的影响。设计正交实验确定了酶辅助法提取透骨草中总黄酮的较佳条件:纤维素酶浓度为2 U/m L、酶解p H=4.5、酶解温度为45℃、酶解时间2 h,总黄酮提取率为1.27%。本文初步探究了透骨草总黄酮提取液对羟自由基的清除活性,对照实验结果表明透骨草提取液对羟自由基清除活性要高于相同浓度的芦丁与二丁基羟基甲苯。     

酶法提取银杏黄酮类化合物研究

本文研究了纤维素酶酶解法提取银杏总黄酮工艺。与传统的乙醇提取工艺相比,银杏总黄酮得率提高了18．92％。实验确定了最佳提取条件：酶浓度0．40mg／mL,酶作用时间120min,酶解温度50℃,酶解介质pH值为4．5,乙醇浓度70％,提取温度70℃。     

纤维素酶提取红景天总黄酮的研究

以总黄酮为考察指标,确定纤维素酶提取红景天有效成分的最佳工艺.研究酶解条件对总黄酮浸出率的影响,并对不同提取方法的提取效果和粗提物的DPPH清除活性进行了比较.纤维素酶提取法的最佳工艺条件为:加酶量为1.95%(以原料干重计),液料比为70∶1(mL∶g),pH值为5.5,酶解温度为40℃,酶解时间为5 h,红景天总黄酮的浸出率为4.385%.酶解技术可明显提高红景天总黄酮的浸出率,粗提物得率高且DPPH清除活性较强.     

超声波协同复合酶法提取姬松茸多糖

研究了超声波协同复合酶法提取姬松茸多糖的最佳工艺条件。采用均匀设计法分别考察不同时间、pH值、温度、酶浓度、固液比对纤维素酶、果胶酶以及木瓜蛋白酶酶解反应的影响,并研究三种酶联合使用时的加酶方式以及超声波协同提取时的最佳条件。结果表明,超声波协同复合酶法可显著提高姬松茸多糖的提取率,其最佳提取条件为：超声波作用20min,分步加酶法（先加果胶酶：pH值3．8、温度50℃、时间90min、加酶量7000U／g、固液比1：45;然后加纤维素酶：pH值3．6、温度75℃、时间120min、加酶量150U／g、固液比1：45;最后加木瓜蛋白酶：pH值3．6、温度75℃、时间120min、加酶量20000U／g、固液比1：45）,多糖提取率达到14．51％。     

壮药山风总黄酮提取工艺的优化研究

采用正交试验对超声辅助提取壮药山风中总黄酮的工艺进行优化,通过考察黄酮的提取温度、乙醇浓度、料液比、提取时间,得到山风总黄酮的最优提取条件为:提取温度80℃、乙醇浓度60%、料液比1∶40 g·mL-1、提取时间20 min,提取率为24.72 mg·g-1,为进一步开发壮药山风的药用及功能性食品利用价值提供理论参考。     

超声波辅助提取山楂籽总黄酮工艺研究

山楂籽是山楂加工业重要副产物,山楂籽富含黄酮类等功效成分,但目前的传统回流提取率相对比较低.基于此,本研究将超声辅助技术应用于山楂籽黄酮提取中.实验结果表明,超声波辅助提取山楂籽总黄酮最优工艺:浸提时间1.5h、超声时间40min、乙醇浓度70%、超声温度65℃、料液比1:18、水浴温度90℃.该条件下,黄酮提取率可达84.3%,与传统回流提取法相比,黄酮提取率提高了15%.     

凤眼莲总黄酮最佳提取条件的探讨

目的：研究从凤眼莲（Eichhornia crassipes）中提取总黄酮的最佳提取条件。方法：以乙醇为溶剂,采用浸提法和超声波法提取凤眼莲总黄酮,通过单因素实验比较两种提取方法;并对黄酮提取物的抗氧化性进行了研究。结果：浸提法提取凤眼莲中总黄酮的最佳工艺条件：乙醇50%、提取温度70℃、提取时间3h、料液比1：40,总黄酮提取率4.30%;超声波法提取凤眼莲总黄酮的最佳工艺条件：乙醇50%、提取时间30min、料液比1：40、超声功率320W,提取率5.09%;凤眼莲总黄酮清除.OH的能力比甘露醇强,而清除.O2-的能力低于Vc。结论：超声波法是提取黄酮类物质较为理想的途径,凤眼莲总黄酮具有一定抗氧化活性。     

半边莲总黄酮提取工艺及抑菌活性的研究

研究了乙醇浓度、料液比、提取温度、提取时间对半边莲中总黄酮提取率的影响,并通过正交实验优化了半边莲中总黄酮的提取工艺条件,结果表明:当乙醇浓度60%,料液比为1∶40(g/m L),提取温度60℃,提取时间2.5 h,从半边莲中提取总黄酮的得率为1.69%。考察了半边莲总黄酮提取物对几种常见微生物的抑菌作用,结果表明半边莲总黄酮提取物具有一定的抑菌活性,对革兰氏阴性菌的抑制作用大于革兰氏阳性菌,低浓度下对青霉菌和酵母菌抑制效果不明显。     

余甘子总黄酮超声波辅助提取工艺的优化

以余甘子干粉为材料,利用超声波辅助提取余甘子总黄酮。单因素试验分析液料比、乙醇浓度、超声时间、超声功率对余甘子总黄酮提取率的影响,在此基础上,利用响应面分析法对提取工艺进行优化。结果表明,余甘子总黄酮最佳提取条件为：液料比82:1(V/W)、乙醇浓度45%、超声时间41 min、超声功率210 W,在此条件下余甘子总黄酮的实际提取率为6.12%。     

酶解破壁促进废次烟叶中茄尼醇溶浸

协同应用纤维素酶和木质素酶催化降解废次烟叶,探讨清洁高效的酶解破壁效应及浸提茄尼醇工艺条件。结果发现复配酶催化裂解溶浸茄尼醇效果明显优于单一酶,酶解时间、温度、pH值以及酶投加量等条件均影响酶破壁浸提茄尼醇能效。结果表明,采用纤维素酶：木质素酶酶活比15∶1 (U/U) 的复配酶,在体积为5倍烟草质量的水介质环境中,当复配酶投加量为175 U/g,水浴温度40 ℃,pH=6时,催化酶解烟叶8 h后,茄尼醇溶浸浓度可达0.33 g/L。在此条件下,茄尼醇平均提取率可达96.53％,是化学回流浸提方法的1.68倍。该方法为有效提取废次烟草中茄尼醇提供了一种新途径。     

槐米芦丁提取技术研究

芦丁作为槐米中黄酮类活性成分的主要代表近年来已得到了人们的高度重视,在简述芦丁的来源、用途、性质的基础上,重点对从槐米原料中提取纯化芦丁的不同方法与技术进行了述评,提出了芦丁提取应注意的问题,为工业化生产和实验室提取芦丁提供了科学的思路.     

Plantlet Regeneration from Leaf Protoplast cultures of Japanese Butterbur

Protoplasts were isolated by enzyme digestion from leaf of Japanese butterbur (Petasites japonicus). The enzyme incubation mixture consisted of 4% (W/V)cellulase RS, 2% (W/V) hemicellulase, 1% (W/V) pectinase-dissolved Y-23 and polygalacturonase in a solution of 0. 5 mol/L mannitol at pH 5.7 . In the basic medium of 1/4 MS inorganic salts and 1/2 MS vitamins supplemented with 2 mg/L NAA, 0. 2–0. 5 mg/L BA, 0. 5 mol/L mannitol and 10 g/L sucrose, the cells divided luxuriantly. Regenerated plantlets were formed from callus after bud induction and root initiation.     

多效唑和缩节胺对现蕾前忍冬枝叶生长及花蕾性状和有效成分含量的影响

以忍冬品种‘九丰一号’(Lonicera japonica‘Jiufeng 1’)为实验材料,采用叶面喷施方法研究了不同质量浓度多效唑和缩节胺对现蕾前(抽枝生长初期)枝叶生长和叶片叶绿素含量以及花蕾性状和花蕾中绿原酸和总黄酮含量的影响。结果显示:分别喷施100、400、700和1 000 mg·L-1多效唑和50、100、150和200 mg·L-1缩节胺后,多数处理组的开花枝条数、着花节数和叶绿素含量较对照CK1(水)有不同程度提高,但叶面积差异不明显。随处理时间延长,各处理组枝条节间长度总体上呈逐渐增加的趋势,其中多数处理组枝条节间长度增长缓慢。各处理的花蕾长度、百蕾鲜质量和干质量总体上小于CK1,而花蕾折干率、总黄酮含量和绿原酸含量显著或不显著高于CK1。此外,在喷施多效唑和缩节胺的同时喷施质量体积分数1.0%尿素和质量体积分数0.1%硼砂,忍冬的叶面积、着花节数、花蕾长度、折干率、百蕾鲜质量和干质量总体上有所提高,而绿原酸含量降低,但各指标的差异总体较小。研究结果表明:喷施适量多效唑和缩节胺可调控忍冬枝条生长,并能提高花蕾中总黄酮和绿原酸含量。     

纤维素酶-超声波协同提取黑木耳黑色素工艺及其抗氧化活性分析

黑色素是黑木耳的主要活性成分之一,在黑木耳的药理活性上发挥着重要作用。为了提高黑木耳黑色素的提取得率,实验采用正交法和响应面法对纤维素酶-超声波协同提取黑木耳黑色素的提取工艺进行了优化,并对最优条件下提取的黑木耳黑色素体外抗氧化活性进行了分析。实验结果表明,纤维素酶-超声波协同提取黑木耳黑色素的最优条件为:酶添加量12mg,酶解温度40℃,酶解pH 5.0,酶解时间120min,NaOH浓度1.27mol/L,料液比1:40,超声功率300W,超声时间52min,超声温度60℃。在最优条件下,黑木耳黑色素提取得率可达到10.48%,相比于实验设置的未添加纤维素酶的超声波组黑色素提取得率提高了12.93%。抗氧化结果表明,采用纤维素酶-超声波协同提取的黑色素相比于未加纤维素酶提取的黑色素清除ABTS、DPPH和羟基自由基的能力更强。研究结果为黑木耳黑色素的高效提取及其产品的应用开发奠定了基础。     

Benefits from tween during enzymic hydrolysis of corn stover

Corn stover is a potential substrate for fermentation processes. Previous work with corn stover demonstrated that lime pretreatment rendered it digestible by cellulase; however, high sugar yields required very high enzyme loadings. Because cellulase is a significant cost in biomass conversion processes, the present study focused on improving the enzyme efficiency using Tween 20 and Tween 80; Tween 20 is slightly more effective than Tween 80. The recommended pretreatment conditions for the biomass remained unchanged regardless of whether Tween was added during the hydrolysis. The recommended Tween loading was 0.15 g Tween/g dry biomass. (The critical relationship was the Tween loading on the biomass, not the Tween concentration in solution.) The 72-h enzymic conversion of pretreated corn stover using 5 FPU cellulase/g dry biomass at 50 degrees C with Tween 20 as part of the medium was 0.85 g/g for cellulose, 0.66 g/g for xylan, and 0.75 for total polysaccharide; addition of Tween improved the cellulose, xylan, and total polysaccharide conversions by 42, 40, and 42%, respectively. Kinetic analyses showed that Tween improved the enzymic absorption constants, which increased the effective hydrolysis rate compared to hydrolysis without Tween. Furthermore, Tween prevented thermal deactivation of the enzymes, which allows for the kinetic advantage of higher temperature hydrolysis. Ultimate digestion studies showed higher conversions for samples containing Tween, indicating a substrate effect. It appears that Tween improves corn stover hydrolysis through three effects: enzyme stabilizer, lignocellulose disrupter, and enzyme effector. Copyright 1998 John Wiley & Sons, Inc.     

Optimization of xylanase production from Aspergillus niger for biobleaching of eucalyptus pulp

A crude endo-xylanase produced by Aspergillus niger BCC14405 was investigated for its potential in pre-bleaching of chemical pulp from eucalyptus. The optimal fermentation conditions on the basis of optimization using response surface methodology included cultivation in a complex medium comprising wheat bran, rice bran, and soybean meal supplemented with yeast extract, glucose, peptone, and lactose with a starting pH of 6.0 for 7 d. This resulted in production of 89.5 IU/mL of xylanase with minor cellulase activity. Proteomic analysis using LC/MS/MS revealed that the crude enzyme was a composite of hemicellulolytic enzymes, including endo-β-1,4-xylanase and other hemicellulolytic enzymes attacking arabinoxylan and mannan. Pretreatment of the pulp at a xylanase dosage of 10 IU/g increased the brightness ceiling after the C-Eop-H bleaching step up to 3.0% using a chlorine charge with a C-factor of 0.16-0.20. Xylanase treatment also led to reduction in chlorine charge of at least 20%, with an acceptable brightness level. The enzyme pretreatment resulted in a slight increase in pulp viscosity, suggesting an increase in relative cellulose content. The crude enzyme was potent in the enzyme-aided bleaching of chemical pulp in an environmentally friendly pulping process.     

The enzymatic hydrolysis and fermentation of pretreated wheat straw to ethanol

Autohydrolysis and ethanol-alkali pulping were used as pretreatment methods of wheat straw for its subsequent saccharification by Trichoderma reesei cellulase. The basic hydrolysis parameters, i.e., reaction time, pH, temperature, and enzyme and substrate concentration, were optimized to maximize sugar yields from ethanol-alkali modified straw. Thus, a 93% conversion of 2.5% straw material to sugar syrup containing 73% glucose was reached in 48 h using 40 filter paper units/g hydrolyzed substrate. The pretreated wheat straw was then fermented to ethanol at 43 degrees C in the simultaneous saccharification and fermentation (SSF) process using T. reesei cellulase and Kluyveromyces fragilis cells. From 10% (w/v) of chemically treated straw (dry matter), 2.4% (w/v) ethanol was obtained after 48 h. When the T. reesei cellulase system was supplemented with beta-glucosidase from Aspergillus niger, the ethanol yield in the SSF process increased to 3% (w/v) and the reaction time was shortened to 24 h.     

Thermostable cellulase production of Aspergillus fumigatus Z5 under solid-state fermentation and its application in degradation of agricultural wastes

A lignocellulosic decomposing fungus Z5 was isolated and identified as Aspergillus fumigatus, its capacity to produce cellulase was assessed under solid-state fermentation (SSF) using lignocellulosic materials as substrates. Cultivation conditions of A. fumigatus Z5 for cellulase production were optimized, results showed that for carboxymethyl cellulase (CMCase) and filter paper enzyme (FPase), the best condition was 50 °C, 80% initial moisture, initial pH 4.0 and 7% initial inoculum, the average activity of CMCase activity, FPase activity reached 526.3 and 144.6 U g⁻¹ dry weight (dw) respectively, much higher than most of previous reports of this genus. Optimal temperature and pH for the CMCase activity of the crude enzyme were found to be 50 °C and 5.0, respectively. Zymogram analysis showed that eight kinds of CMCase were secreted by A. fumigatus Z5 when cellulose-containing materials were supplied in the culture. The crude enzyme secreted by the strain was further applied to hydrolyze pretreated corn stover and the enzymatic hydrolysate was used as substrate for ethanol production by Saccharomyces cerevisiae. The yield of bio-ethanol was 0.112 g g⁻¹ dry substrate (gDS), suggesting that it is a promising fungus in the bio-ethanol production process.     

麝香石竹花芽离体发育的阶段控制

在离体条件下,利用不同的培养基对麝香石竹顶芽外植体的花芽发育进行了阶段控制的研究.结果表明,麝香石竹的顶芽外植体在MS+KT1.0mg/L+IAA1.0mg/L+蔗糖3.0%+琼脂0.8%的Ⅰ级培养基上能被诱导花芽发育的启动;然后,将已诱导花芽发育启动的顶芽外植体,转接到MS+KT1.0mg/L+IAA0.5mg/L+蔗糖1.5%+葡萄糖1.5%+琼脂0.8%的Ⅱ级培养基上能进行花芽的进一步发育形成花蕾,且能从一个花蕾继续分化发育重新产生2—3个花蕾;把花蕾再转接到改良的MS+BA2.0mg/L+NAA0.2mg/L+蔗糖1.5%+葡萄糖1.5%+琼脂0.8%的Ⅲ级培养基上,培养一周后花蕾的花瓣张开,花朵全部开放.不同麝香石竹品种,诱导花芽发育启动的效果不同,Scania品种诱导效果最好.花芽发育初期可溶性蛋白含量较高,但随着花芽发育的进程而迅速下降,不同花芽发育时期的过氧化物酶活性均强于营养器官.本文为花芽分化发育机理的研究创造了条件,也为鲜花生产探索了新路子.