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1.
研究对前期筛选的一株产木聚糖酶菌株L10608进行鉴定,判定其为链霉菌。并对该菌株所产木聚糖酶进行纯化得到电泳级纯度木聚糖酶L10608-Xyn11。该酶蛋白质分子量为24 k Da。探究L10608菌株所产木聚糖酶以商品玉米芯木聚糖、商品燕麦木聚糖、自制水不溶性玉米芯木聚糖为底物时的水解特性,结果表明该菌所产木聚糖酶对木三糖有很强的水解作用,以自制水不溶性玉米芯木聚糖为底物水解时效果最为明显,底物中木三糖的含量下降了1.521 mg/m L,产物中木二糖增加了1.635 mg/m L,木糖仅增加了0.180 mg/m L。菌株L10608的酶解产物中低聚木糖的产量远高于木糖,且高产低聚木糖中的主要有效成分木二糖,其水解特异性表明该菌有潜力作为益生元型低聚木糖的生产菌株。  相似文献   

2.
本文研究了卷须链霉菌(StreptomycescirratusD-10)木聚糖酶水解玉米芯汽爆液,碱提玉米芯木聚糖的合适酶用量和酶水解时间,分别为80U/100mL,6h和60u/g,8h。同时以玉米芯粉作为酶解对照。表明玉米芯不同处理底物,汽爆液水解率最高,碱提玉米芯木聚糖水解率次之。酶解产物经TLC分析表明卷须链霉菌D-10酶解产物以木二糖和木三糖为主,产物中没有阿拉伯糖,玉米芯汽爆液酶解产物中含有微量的阿拉伯糖。  相似文献   

3.
本文以橄榄绿链霉菌E-86产木聚糖酶水解玉米芯汽爆液生产低聚木糖为目的,研究了玉米芯汽爆液的水解特征,并与玉米芯木聚糖的酶解产物组成进行了比较,得到如下结果:加酶量120U/100ml、酶解反应8h可获得较好的酶解效果,直接还原糖量46μmol/ml、平均聚合度3.1、水解率46%;玉米芯汽爆液和玉米芯木聚糖的酶解产物中低聚糖组成大致相同,主要是木二糖和少量的木三糖、木糖,汽爆液酶解产物中还含有极少量的鼠李糖和阿拉伯糖:玉米芯汽爆液可代替玉米芯木聚糖为底物生产低聚木糖。  相似文献   

4.
不同原料酶法制备低聚木糖的研究及成分分析   总被引:1,自引:0,他引:1  
对木聚糖酶的酶学特性进行了研究,同时以甘蔗渣、玉米芯、麸皮、啤酒槽为原料酶解制备低聚木糖并对其酶解液的还原糖含量和主要成分进行了分析。结果表明:该木聚糖酶的最适反应温度为60℃,最适反应pH为5.0;同时在温度为40~60℃和pH为6的情况下,木聚糖酶具有较好的稳定性。在最佳酶解条件下,采用木聚糖酶酶解甘蔗渣、玉米芯、麸皮、啤酒槽中的木糖,通过测定酶解液中的还原糖含量以分析木聚糖的水解度,结果表明,麸皮中木聚糖的水解度最高,为21.19mg/mL;其它依次为啤酒糟、玉米芯、蔗渣。采用高效液相色谱法对4种不同原料的木聚糖酶水解产物进行分析,结果显示:啤酒糟的酶解产物中木二糖和木三糖的相对含量最高,分别为13%、26.7%,其他依次为玉米芯、麸皮、甘蔗渣。  相似文献   

5.
朱运平  禇文丹  李秀婷  滕超  李娥  杨然 《食品科学》2012,33(21):177-182
以木聚糖为唯一碳源制作选择培养基,利用透明圈法筛选高产木聚糖酶菌株,对其中一株产酶较高的菌株L10608进行液体发酵条件优化并对所产木聚糖酶的水解特性进行研究。结果表明:菌株L10608最佳产酶条件为以质量浓度25g/L、80目的水不溶性玉米芯木聚糖为碳源,10g/L大豆蛋白胨和5g/L酵母浸膏为复合氮源,初始pH6.0、培养温度40℃、转速200r/min、表面活性剂吐温-80质量浓度4g/L,最佳产酶条件下木聚糖酶活力达1074.8U/mL。以桦木木聚糖、榉木木聚糖和燕麦木聚糖为底物研究菌株L10608所产木聚糖酶的水解特性,结果表明该木聚糖酶为内切型木聚糖酶,水解主要产物为木二糖和木三糖。表明菌株L10608有望作为功能性低聚木糖的生产菌株。  相似文献   

6.
研究了在4℃条件下,由橄榄灰绿链霉菌(StreptomycesolivaceovirdisE-86简称sp.E-86)产木聚糖酶分别在木质纤维玉米芯成分:纤维素、木聚糖、木质素、全纤维素和玉米芯粉上的吸附动力学以及吸附90min时的吸附等温线。结果表明,该木聚糖酶在这些木质纤维上很快达到平衡,除木聚糖在1h达到平衡外,其它都不超过30min;吸附等温线都符合两阶段非均匀表面吸附模型;在所有吸附等温线中,玉米芯吸附量最大,纤维素最小;在三种纤维中,全纤维素吸附量最大、木聚糖次之、纤维素最小。  相似文献   

7.
考察了试验室规模下超声波处理玉米芯提取木聚糖经酶水解制备低聚木糖的影响因素,通过单因素试验和正交试验,优化了提取和水解条件。结果表明:以质量分数5%Na OH溶液为提取剂,超声功率为180 W,超声温度为60℃的条件下提取45 min,木聚糖产率可达到33.18%。所得提取液经脱色,调p H,调木聚糖底物浓度后酶水解制备低聚木糖。最佳酶解条件为:木聚糖底物质量浓度10 mg/m L,加酶量质量分数1.5%(相对于玉米芯干物料),酶水解时间为8 h的条件下,水解液中还原糖的质量浓度达到6.89 mg/m L。  相似文献   

8.
为研究碱法提取玉米芯中水不溶性木聚糖的优化条件及产物组成,用单因素试验评价预处理温度、NaOH浓度、料液比、提取温度与时间对提取率的影响之后,通过正交试验L16(45)确定最佳提取条件是:40℃预煮,15%NaOH溶液,固液比1∶15,100℃提取4 h,过滤,调节滤液pH值至7.0,静置过夜后离心得沉淀,洗涤沉淀,烘干后即得水不溶性木聚糖。在上述条件下玉米芯水不溶性木聚糖提取率为20.86%。对碱法提取的玉米芯水不溶性木聚糖进行木聚糖酶水解及产物分析,结果几种木聚糖酶均能使水不溶性木聚糖产生木二糖、木三糖及木四糖含量较高的低聚糖。  相似文献   

9.
《食品与发酵工业》2015,(4):115-120
研究了蒸煮法及碱提法对玉米芯木聚糖的提取效果,并利用重组木聚糖酶Xyn A对玉米芯低聚木糖的酶解制备条件进行了优化。对木聚糖得率及酶解产物进行了分析,确定碱提法所得玉米芯木聚糖适宜作为酶解底物制备低聚木糖。优化后得到酶解制备玉米芯低聚木糖的工艺条件:底物浓度0.9%,酶解温度49℃,酶解时间4.5 h,还原糖量可达33.9%。另外,对酶解成分进行分析,结果表明酶解碱提玉米芯木聚糖可产生以木二糖及木三糖为主要成分的低聚木糖。  相似文献   

10.
以玉米芯为原料的低聚木糖生产包括原料的稀酸预处理,蒸煮和酶法水解等过程,本文采用凝胶过滤色谱研究玉米芯木降糖在整个过程中的分子结构的变化。研究结果表明,在选定的稀酸预处理条件下木聚糖不会降解;蒸煮时木聚糖发生随机降解,蒸煮温度越高,降解程度越大,135℃蒸煮30min,大部分木聚糖已有相当程度的降解,但它们的相对分子质量仍然大于1500,该蒸煮条件可满足低聚木糖生产要求;蒸煮液(连渣)加木聚糖酶水解得到的产品的主要成分为木二糖和木三糖等低聚木糖。  相似文献   

11.
采用可逆溶解性聚合物Eudragit L-100对球毛壳菌木聚糖酶进行了吸附固定化。在1.0%Eudragit L-100浓度时获得10.6IU/mg载体的固定化酶活和88.47%的酶活回收。酶固定化后最适温度不变,最适pH向碱性方向移动了一个pH单位。固定化酶热稳定性和操作稳定性显著提高,循环利用6次仍保留65%初始酶活。木聚糖水解产物测定表明,在同酶用量的条件下固定化后总还原糖产量明显高于游离酶,二者水解产物均以低聚糖为主,酶固定化后水解产物木二糖含量显著高于游离酶,成为主要的产物。木聚糖酶固定化后各方面特性明显优于游离酶,在低聚糖生产中有实际应用价值。  相似文献   

12.
BREAKDOWN OF XYLAN BY ENZYMES FROM HUMAN COLONIC BACTERIA   总被引:2,自引:0,他引:2  
Xylan from Larchwood was utilized as a carbon source by three species of Bacteroides from the human colon: Bacteroides ovatus, Bacteroides eggerthii and Bacteroides fragilis subsp. a. Xylan-degrading enzymes of all three species were cell-associated rather than extracellular, i.e. xylanase activity was detected in sonically disrupted bacteria but not in the extracellular fluid. The state of hydration of the xylan was an important factor in determining the extent to which the xylan was hydrolyzed by the bacterial enzymes. When xylan which had been partially hydrated by autoclaving was subjected to centrifugation at 17,000 xg for 20 min at 40C, a portion of the xylan was pelleted. This portion, which was presumably less well hydrated than the xylan which remained in solution, was not digested at all by the bacterial enzymes. By contrast, xylan which remained soluble after centrifugation (soluble xylan) was degraded by bacterial xylanases. Xylose was the main product of digestion, although traces of arabinose, glucose and higher oligomers of xylose were also detected. Even after exhaustive hydrolysis, less than 60% of the soluble xylan was hydrolyzed. Removal of most of the arabinose branches did not increase the extent of hydrolysis. Moreover, the carbohydrate composition of the portion of the soluble xylan which resisted hydrolysis was the same as the composition of the xylan which was hydrolyzed. Thus it is likely that hydrolysis was limited by aggregate formation rather than by structural features such as arabinose branches.  相似文献   

13.
建立一种木聚糖酶活力的微量测定新方法——3-甲基-2-苯并噻唑酮腙(MBTH)法。根据木聚糖及其酶解产物的特殊性,研究MBTH法的显色条件,并以多点测定法对酶活力测定中的几个关键参数进行探讨。结果表明:蛋白质在其质量浓度低于30μg/mL时对测定无干扰;木聚糖溶液的最佳测定质量浓度为4mg/mL;较高的酶解温度会使木聚糖酶在测定过程中失活,因此,酶活力测定的最佳温度为30℃,而远低于该酶的最适温度;酶解时间为60min以内;酶解产物与MBTH试剂的反应时间应控制在13~16min之间,以15min为最佳。以酶解时间为30min计,本法检测限为0.135mU/mL,定量限为0.451mU/mL,适当延长酶解时间可相应提高酶活力检测灵敏度。该法准确度高,结果稳定,灵敏度远高于DNS法。  相似文献   

14.
We functionally characterized the GH10 xylanase (SoXyn10A) and the GH11 xylanase (SoXyn11B) derived from the actinomycete Streptomyces olivaceoviridis E-86. Each enzyme exhibited differences in the produced reducing power upon degradation of xylan substrates. SoXyn10A produced higher reducing power than SoXyn11B. Gel filtration of the hydrolysates generated by both enzymes revealed that the original substrate was completely decomposed. Enzyme mixtures of SoXyn10A and SoXyn11B produced the same level of reducing power as SoXyn10A alone. These observations were in good agreement with the composition of the hydrolysis products. The hydrolysis products derived from the incubation of soluble birchwood xylan with a mixture of SoXyn10A and SoXyn11B produced the same products as SoXyn10A alone with similar compositions. Furthermore, the addition of SoXyn10A following SoXyn11B-mediated digestion of xylan produced the same products as SoXyn10A alone with similar compositions. Thus, it was hypothesized that SoXyn10A could degrade xylans to a smaller size than SoXyn11B. In contrast to the soluble xylans as the substrate, the produced reducing power generated by both enzymes was not significantly different when pretreated milled bagasses were used as substrates. Quantification of the pentose content in the milled bagasse residues after the enzyme digestions revealed that SoXyn11B hydrolyzed xylans in pretreated milled bagasses much more efficiently than SoXyn10A. These data suggested that the GH10 xylanases can degrade soluble xylans smaller than the GH11 xylanases. However, the GH11 xylanases may be more efficient at catalyzing xylan degradation in natural environments (e.g. biomass) where xylans interact with celluloses and lignins.  相似文献   

15.
极耐热性阿拉伯糖苷酶在木糖制备中的应用   总被引:1,自引:1,他引:0  
阿拉伯糖苷酶作为木聚糖降解的限速酶之一,在植物残体的生物转化、食品加工、饲料工业以及纸浆漂白中具有广泛的应用潜力。实验中选择pET—28a作为表达载体,优化核糖体结合位点RBS与起始密码子ATG间距离,使来自海栖热袍菌(Thermotoga maritima)极耐热性阿拉伯糖苷酶得到高效表达,重组酶蛋白经一步热处理后纯度达到90%以上;木聚糖酶解试验结果表明,阿拉伯糖苷酶和木聚糖酶间存在协同作用;阿拉伯糖苷酶与木聚糖酶和β-木糖苷酶联合水解木聚糖能明显提高酶解产物中木糖含量,因此,开发极耐热性阿拉伯糖苷酶在酶法制备木糖中的应用具有重要的经济效益和社会效益。  相似文献   

16.
Sugarcane bagasse is a useful biomass resource. In the present study, we examined the efficacy of ammonia pretreatment for selective release of hemicellulose from bagasse. Pretreatment of bagasse with aqueous ammonia resulted in significant loss of xylan. In contrast, pretreatment of bagasse with anhydrous ammonia resulted in almost no xylan loss. Aqueous ammonia or anhydrous ammonia-pretreated bagasse was then subjected to enzymatic digestion with a xylanase from the glycoside hydrolase (GH) family 10 or a xylanase from the GH family 11. The hydrolysis rate of xylan in bagasse pretreated with aqueous ammonia was approximately 50 %. In contrast, in the anhydrous ammonia-treated bagasse, xylan hydrolysis was > 80 %. These results suggested that anhydrous ammonia pretreatment would be an effective method for preparation of sugarcane bagasse for enzymatic hydrolysis to recover xylooligosaccharides.  相似文献   

17.
从顶青霉(Penicillium corylophilum)培养液中分离纯化得到的3种木聚糖酶组分(Part A,Part B和Part C),对其水解动力学和水解模式的研究结果表明,3种木聚糖酶的动力学常数(桦木木聚糖为底物)分别为Part A,K  相似文献   

18.
木聚糖酶能选择性地水解纸浆中的木聚糖,提高纸浆的可漂性,从而使漂白化学品更容易与木素作用。木聚糖酶助漂在一定程度上节约了漂白化学药品用量,减少了化学漂白过程对环境的污染。本文对木聚糖酶在纸浆漂白中漂白机理的研究现状进行了归纳和评述,并对木聚糖酶辅助漂白技术的发展进行了展望。  相似文献   

19.
嗜热拟青霉利用玉米芯产木聚糖酶的发酵条件优化   总被引:1,自引:0,他引:1  
以一株新的嗜热拟青霉(Paecilomyces thermophila)J18为出发菌株,对其液态发酵产木聚糖酶的条件进行了优化。结果表明,以玉米芯为碳源能高效诱导木聚糖酶的胞外分泌,胰蛋白胨为最佳氮源,初始pH和培养温度分别为pH 7.5,50℃,所得酶活力最高。在优化后的培养基和培养条件下,第5 d酶活力达到峰值,为1 276 U/mL,表明该拟青霉能够利用农业废弃物高效生产木聚糖酶。该酶水解桦木木聚糖主要生成木二糖和木三糖,适合生产低聚木糖。  相似文献   

20.
玉米芯木聚糖的酶法降解及产物的分离纯化   总被引:1,自引:0,他引:1  
李新宇  张红梅 《饮料工业》2007,10(10):31-35
以自制玉米芯木聚糖为原料,采用单一及复合木聚糖酶处理,研究其对降解产物产率的影响,比较了不同的分离纯化方式对降解产物得率的影响,并采用HPAEC图谱分析产物纯度。研究结果表明,单一木聚糖酶降解能力较差,而在两种木聚糖酶共同作用下的低聚木糖得率不仅能增加木二糖和木三糖的产率,也能大幅减少一般的反应时间。活性炭与硅藻土法批式分离木聚糖酶解液总回收率约在20%左右,并且木二糖较多出现在活性炭CJ组5%以下的EtOH冲提液内;将1.0%玉米芯木聚糖酶水解液依序通过不同分子量切,最后经1kDa薄膜过滤后可收得聚合度7以下的低聚木糖产物11.5% ̄15.2%;活性炭!硅藻土混合管柱连续分离低聚木糖,活性炭CJ组5%乙醇冲提管柱可获得13%的木二糖,经HPAEC图谱分析连续式分离能得到纯度较高的单一低聚木糖划分物,但是其回收率不及批式分离的高。  相似文献   

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