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1.
采用离心、层析和电泳等方法研究了多粘芽孢杆菌T1163在红麻干皮、鲜皮和鲜茎三种材料和振荡、静置两种发酵体系中分泌的脱胶酶种类,结果表明:红麻专用脱胶菌株T1163在脱胶过程中中至少产生9种脱胶酶(和亚基),其中分子量为70800D、61600D、60000D、51200D、43000D41700T在33500D的七种酶在两种体系中共同存在,分子量为56300D和28800D的两种酶分别只存在于振荡、静置系,不同酶在脱胶过程中产生的时间、速度和数量随红麻材料和发酵方式的不同存在不同程度的差别。  相似文献   

2.
采用离心、层析和电泳等方法研究了多粘芽胞杆菌 T1 1 6 3在红麻干皮、鲜皮和鲜茎三种材料和振荡、静置两种发酵体系中分泌的脱胶酶种类 ,结果表明 :红麻专用脱胶菌株 T1 1 6 3在脱胶过程中至少产生 9种脱胶酶 (和亚基 ) ,其中分子量为 70 80 0 D、6 1 6 0 0 D、6 0 0 0 0 D、5 1 2 0 0 D、430 0 0 D、41 70 0 D和 335 0 0 D的七种酶在两种体系中共同存在 ,分子量为5 6 30 0 D和 2 880 0 D的两种酶分别只存在于振荡、静置系。不同酶在脱胶过程中产生的时间、速度和数量随红麻材料和发酵方式的不同存在不同程度的差别。  相似文献   

3.
红麻微生物发酵过程中胶胶酶的特性研究   总被引:3,自引:0,他引:3  
采用一株多粘芽孢杆菌对红麻博士、鲜皮和鲜茎3种材料在振荡、静置2种发酵体系中脱胶酶的活性变化和作用特性进行了研究,结果表明:(1)同一材料在发酵对应时段,振荡系的酶活均较静置系的高,在干皮和鲜皮脱胶过程中,果胶酶活的峰值出现较半纤维素酶活的早,鲜茎则相反,峰值过后酶活变化幅度较小;(2)混合酶系中果胶和半纤维素酶作用的最适温度均为50℃,最适pH分别为8.0,4.4;(3)用豆饼粉培养基静置培养24h的粗酶液接种4.0mL可在30h内完成干皮脱胶。  相似文献   

4.
利用红麻专用脱胶菌T1163 分别在振荡和静置条件下,对红麻鲜皮进行了脱胶试验,测定了发酵液中的活菌量、pH 值、挥发酸、COD、还原糖、胞外可溶蛋白及脱落物量和总残渣量等指标。结果表明,在振荡条件下,54h 内完成红麻鲜皮脱胶;微生物在0~12h 旺盛繁殖;pH 值为6.5 ~7 .5;挥发酸峰值为236mg/l;COD在6h 出现峰值,为958mg/l;还原糖在0~24h 迅速下降。在静置条件下,48h 内完成红麻鲜皮脱胶;T1163 活菌量在6h 左右出现一个“低谷”;pH 值为5.0 ~6.0 ;挥发酸峰值为1920mg/l,COD和还有糖分别在12h 和6h 左右出现峰值。两种发酵体系中,脱落物和总残渣量均随着脱胶时间延长而增加,至完成脱胶时分别占麻重的18.51% ~20.05% 和4.1% ~5.52% ;可溶性蛋白质变化规律均类似于“M”型。  相似文献   

5.
利用红麻专用脱胶菌T1163分别在振荡和静置条件下,对红麻鲜茎进行了脱胶试验,测定了发酵液中的活菌量、pH值、挥发酸、COD、还原糖、胞外可溶蛋白及脱落物和总残渣量等指标.结果表明,在振荡条件下,84小时完成红麻鲜茎脱胶;pH值为6.80~7.45;挥发酸和可溶蛋白含量较低,其峰值分别为148mg/l和53mg/l.在静置条件下,72小时完成红麻鲜茎脱胶;pH值为6.20~6.80;挥发酸随脱胶的进程而不断增加,脱胶完成时下降,峰值635mg/l;胞外可溶蛋白变化趋势呈"M"型.两种发酵体系中,脱落物和总残渣量均随脱胶时间延长而呈不断增加趋势,脱胶完成时,其去除率均达11%左右;微生物均在2-6小时迅速旺盛繁殖;COD和还原糖均呈"M"型趋势.  相似文献   

6.
利用红麻专用脱胶菌T1163 分别在振荡和静置条件下 ,对红麻鲜茎进行了脱胶试验 ,测定了发酵液中的活菌量、pH值、挥发酸、COD、还原糖、胞外可溶蛋白及脱落物和总残渣量等指标。结果表明 ,在振荡条件下 ,84小时完成红麻鲜茎脱胶 ;pH值为 6 .80~ 7.45 ;挥发酸和可溶蛋白含量较低 ,其峰值分别为 1 48mg/l和 5 3mg/l。在静置条件下 ,72小时完成红麻鲜茎脱胶 ;pH值为 6 .2 0~ 6 .80 ;挥发酸随脱胶的进程而不断增加 ,脱胶完成时下降 ,峰值 6 35mg/l;胞外可溶蛋白变化趋势呈“M”型。两种发酵体系中 ,脱落物和总残渣量均随脱胶时间延长而呈不断增加趋势 ,脱胶完成时 ,其去除率均达 1 1 %左右 ;微生物均在 2— 6小时迅速旺盛繁殖 ;COD和还原糖均呈“M”型趋势。  相似文献   

7.
从红麻田土壤中分离到一株多粘芽孢杆菌(Bacillus polymyxa)T1163,这株菌可在36小时内使红麻脱胶,96小时内基本脱掉黄麻胶质。系统研究了这株菌的适宜培养条件,并采用湿润发酵方式进行了红麻接种T1163菌的小型脱胶试验。结果表明,在有杂菌干扰下,脱胶红麻干皮只需3天时间,比传统的天然脱胶法缩短7天以上,并大大减少纤维损失,使精洗率提高5.7%。文中还就T1163的分类、培养及发酵条件和湿润加菌脱胶法的经济、生态效益等问题进行了讨论。  相似文献   

8.
从红麻田土壤中分离到一株多粘芽孢杆菌(Bacillus polymyxa)T1163,这株菌可在36小时内使红麻脱胶,96小时内基本脱掉黄麻胶质。系统研究了这株菌的适宜培养条件,并采用湿润发酵方式进行了红麻接种T1163菌的小型脱胶试验。结果表明,在有杂菌干扰下,脱胶红麻干皮只需3天时间,比传统的天然脱胶法缩短7天以上,并大大减少纤维损失,使精洗率提高5.7%。文中还就T1163的分类、培养及发酵条件和湿润加菌脱胶法的经济、生态效益等问题进行了讨论。  相似文献   

9.
利用红麻专用脱胶菌T1163分别在振荡和静置条件下,对红麻鲜皮进行了脱胶试验,测定了发酵液中的活菌量、PH值、挥发酸、COD、还原糖、胞外可溶蛋白及脱落物量和总残渣量等指标。结果表明,在振荡条件下,54小时内完成红麻鲜皮脱胶;微生物在0~12小时旺盛繁殖;PH值为6.5~7.5;挥发酸峰值为236mg/l,COD在6小时出现峰值,为958mg/l;还原糖在0~24小时迅速下降。在静置条件下,48小  相似文献   

10.
不同脱胶菌株胞外酶系研究   总被引:1,自引:0,他引:1  
运用SDS—PAGE法,通过系统研究T85—260、T1163、T66等3株脱胶菌株在纯培养、灭菌和未灭菌苎麻脱胶过程中的胞外酶系,初步明确了T85—260的胞外酶为组成型,而其它两种菌株的胞外酶为诱导型,T85—260存在较多种类脱胶关键酶,表达量多,而其它两种菌脱胶关键酶种类和表达量都少。T85—260的快速脱胶机理也作了分析。  相似文献   

11.
不同脱胶菌株胞外酶系研究   总被引:2,自引:0,他引:2  
运用SDS-PAGE法,通过系统研究T85-260、T1163、T66等3株脱胶菌株在纯培养、灭菌和未灭菌苎麻脱胶过程中的胞外胶过程中的胞外酶系,初步明确了T85-260的胞外酶为组成型,而其它两种菌株的胞外酶为诱导型,T85-260存在较多种为在脱胶关键酶,表达量多,而其它两种菌脱腕关键酶种类和表达量都少。T85-260的快速脱胶也作了分析。  相似文献   

12.
利用亨氏厌氧技术从沤麻塘底泥等厌氧生境中分离筛选到N2,Y4,Z2-6三株厌氧细菌,研究结果表明,其产酶最适pH为7.0-7.4,最适温度为30℃,最佳碳源为淀粉,最佳氮源为豆饼粉。N2、Y4、Z2-6的果胶酶活分别为:913u,973u,927U,半纤维素酶活分别为:137u、140u、170u,纤维素酶活分别为0、3u、0,对数生长期均为5-9小时,产酶高峰时间均在72小时左右。三个菌株混合发酵红麻皮,5天可成浆,粗浆得率为74.4%,半纤维素脱除率为28.79%,果胶脱除率为72.41%,脂蜡质脱除率为23.23%,打浆后做手抄片,白度为40.5,裂断长为3529m。对N2,Y4,Z2-6进行了初步鉴定,经查《伯杰细菌鉴定手册》第八版,三个菌株均属梭菌属的群Ⅲ。  相似文献   

13.
红麻亲本与杂交组合产量、品质性状的遗传效应分析   总被引:8,自引:0,他引:8  
采用双列杂交遗传设计和加性-显性遗传模型,分析了7个红麻杂交亲本和21个F1组合的11个产量与品质性状,结果表明:(1)株高、鲜皮厚、千粒重、纤维支数同时受到加性和显性效应的控制;而茎粗、单株干皮重、单株干茎重、皮骨比、出麻率、单株纤维重、精洗率、纤维强力主要受显性效应控制。(2)对红麻亲本遗传效应估测结果表明,各亲本不同性状的遗传效应不同。可根据亲本对每个性状的不同遗传效应表现,在育种和杂种优势利用上加以选择利用。综合分析表明,福红2号、福红992和非洲裂叶3个亲本具有提高株高、茎粗、鲜皮厚、单株干皮重、单株干茎重、出麻率、皮骨比、精洗率、单株纤维重的正向遗传效应:福红2号和福红9922个亲本还具有提高纤维强力与纤维支数的遗传效应。上述结果可为红麻遗传改良和杂种优势利用提供一定的科学依据。  相似文献   

14.
在天然水浸脱胶条件下,对影响亚麻脱胶效果的麻茎特性及其作用机制进行了初步探讨。结果表明,麻茎上带有脱胶能力较强的微生物,能加速亚麻脱胶进程;麻茎的部位、粗细、麻龄等不同,其纤维及胶质的组成和分布也有差异,对亚麻的脱胶速度均产生不同程度的影响;机械破损能够破坏麻茎的表皮结构,增大脱胶酶的侵袭面积,能加快亚麻的脱胶速度。  相似文献   

15.
Kenaf (Hibiscus cannabinus) grown in northern Mississippi and elsewhere often is injured by early frost and killed before harvest. Frost kill often is associated with fungal growth or rot, so its effect on fiber quality is a major concern. Fiber processing also affects the quality and chemical composition of fibers. Therefore, this study was aimed at determining the effects of frost kill on processing, fiber quality and chemical composition of kenaf fibers. Frost-damaged kenaf with fungal growth was decorticated by hand and divided into six sections (26.88 cm/each) from the base to tip of the stem and then retted chemically or bacterially in the laboratory. Fiber characteristics were compared between the two processes and the six locations on the plant. Ash, cellulose, hemicellulose, and lignin contents of the resultant fibers were measured. Bacterially retted (BR) fibers were stronger (11.8 g/tex) than the chemically retted fibers (CR), 7.5 g/tex, at all locations. The BR fibers from decorticated green ribbons were stronger than those from frost-killed ribbons. However, no significant differences occurred between the CR fibers from decorticated and frost-killed ribbons. Residual gum content was higher for the BR fibers (23.3%) than for the CR fibers (8.1%). The stretch properties were not affected significantly by the frost kill or fungus. The base of the stem had the weakest fibers in both processes, which may have been due to greater fungal disease. The CR process extracted more fiber than the BR process, with a consistent higher yield of clean fibers. In the BR process, the fiber extracted was higher at the tip than at the base of the stem. This may have been related to the presence of fungus, which inhibits the BR process. Analysis of chemical composition of the processed fibers indicated that CR is efficient in reducing hemicellulose and lignin contents. These results indicate that frost kill may not be the appropriate method for harvesting kenaf for quality fibers. However, fibers extracted by chemical retting were unaffected by the presence of fungus as a result of frost kill.  相似文献   

16.
红麻种质资源遗传变异和亲缘关系的RAPD分析   总被引:8,自引:6,他引:8  
用随机扩增多态DNA(RAPD)方法对红麻种质资源的遗传变异和亲缘关系进行分析。6个引物对14份日本使用的红麻品种扩增出总共30条RAPD多态性条带。根据RAPD图谱模式可将红麻品种区分开来,区分范围从6份(用OPA-20引物扩增)到12份(用OPA-11引物扩增)的品种。用这30条多态性条带构建出的聚类分析树状图,将这14份红麻品种聚成源于印度、中国、越南的三大类。在随后进行的用四个引物对19份从美国引入的红麻种质资源的RAPD分析中,获得以35条多态性条带为基础的RAPD图谱并构建了树状图。结果认为这19份材料的大部分源于EI Salvador种系。起源相近或亲本来源相同的红麻品种资源随着时间、环境和人为等因素的影响农艺性状不断变异,但在DNA分子水平上的变异相对较小。根据红麻的农艺性状等很难判定品种的来源,而RAPD方法可区分鉴定品种以及明确品种资源间的亲缘关系。  相似文献   

17.
Process parameters such as gelation and curing temperatures are parameters that influence the pultruded kenaf reinforced vinyl ester composites profile quality and performance. The effect of gelation and curing temperatures on mechanical (tensile, flexural and compression properties) and morphological properties of pultruded kenaf reinforced vinyl ester composites were analyzed. Obtained results indicated that increase of gelation and curing temperatures during the pultrusion process of kenaf reinforced vinyl ester composites influenced the mechanical properties of the composites. When the gelation and curing temperatures were increased, tensile strength, tensile modulus, flexural strength, flexural modulus and compressive strength were affected and they were either increased or decreased. The factors that influenced these results include improper curing, excessive curing, water diffusion, and the problems associated with interfacial bonding between fibre and matrices. The optimum values of the tensile strength for gelation and curing temperatures of kenaf pultruded composites were at 100 °C and 140 °C, tensile modulus at 80 °C and 180 °C, flexural strength at 100 ° and 140 °, flexural modulus at 120 ° and 180 °, and compressive strength at 120 °C and 180 °C, respectively. The scanning electron micrographs of tensile fractured samples clearly show that with the increase in gelation temperature, it creates the lumens between matrix and kenaf fibre thus reducing tensile properties whereas increasing the curing temperature caused less fibre pull out and enhanced fibre/matrix interfacial bonding.  相似文献   

18.
麻类生物脱胶与生物制浆酶系   总被引:7,自引:0,他引:7  
本文对麻类生物脱胶与生物制浆的三类主要酶类,即果胶酶、半纤维素酶(甘露聚糖酶、木聚糖酶)和木质素降解酶进行了比较全面的总结,对其应用前景也进行了评论。  相似文献   

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