苎麻织物的纤维素酶处理的研究

阐述了纤维素酶减量的作用原理，对苎麻织物的纤维素酶处理工艺和结果进行了讨论，确立了最佳工艺：酶用量2%owf，温度50～55℃，pH值5～5.5，苎麻织物用纤维素酶处理后结合用氨基硅微乳液处理，能改善外观、手感和悬垂性，基本解决刺痒感问题。     

从烟草悬浮细胞中分离液泡前体的方法研究

通过跟踪含有液泡前体特异标记物的组分, 利用细胞壁酶水解胞壁制造原生质体, 并用真针头挤压的方法裂解细胞, 用蔗糖密度梯度离心的方法分离液泡前体. 通过相差显微镜观察, 发现所分离的液泡前体保持完整的结构. 利用不同细胞器的标记物抗体进行免疫标记检测, 证明所纯化的液泡前体不含其他细胞器, 具有较高的纯度.     

Protein Extraction from Heat-stabilized Defatted Rice Bran: II. The Role of Amylase, Celluclast, and Viscozyme

ABSTRACT: The effectiveness of 3 carbohydrases for protein extraction from heat-stabilized defatted rice bran (HDRB) was evaluated. Amylase, viscozyme and celluclast extracted a maximum of 45.4, 12.1, and 28.5% protein, respectively. Further study showed that extracted protein ranged from 9.5 to 58.4% under conditions of water to bran ratio (5:1 to 20:1), α-amylase (0 to 110000 units/10 g rice bran), temperature (35 to 55 °C), and time (1 to 8 h). The maximum protein extracted was 58.4% with a water to bran ratio of 17:1, 87637 units amylase, and 50.9 °C. These results suggest that impure food-grade amylase containing protease is more effective than celluclast and viscozyme in protein extraction from HDRB.     

纤维素酶分子的计算机辅助序列分析

利用生物大分子数据库（EMBL、SWALL和PDB）及软件技术（DNASIS和AntheProt）对嗜热子囊菌（Thermoascus aurantiacus)的产生的一种纤维素酶分子进行了序列分析及结构预测；通过多种来源的纤维素酶的比较研究，分析了其催化区、活性位点及局部保守序列。     

Improved cellulase production by stable Clostridium cellulolyticum mutants

Methods for the production of mutants of the cellulase producer Clostridium cellulolyticum ATCC 35319 were examined using an agar plate screening technique. Spontaneous and UV light-induced mutants were isolated, some of which exhibited a high level of both endoglucanase and exoglucanase activities as assayed using CMC (carboxymethyl cellulose) and PNPCb (paranitrophenyi-β-cellobioside) respectively. The volumetric enzyme activities were up to 2.5 times those of the wild strain.     

丝状真菌纤维素酶合成机制的研究

丝状真菌产生的纤维素酶被认为是最有应用前景的,但就目前酶生产效率来看,离实际应用还有很大的差距,需要对酶的合成调节机制有更为全面和深刻的了解。纤维素酶的生物合成受诱导和阻遏双重控制,酶的生产既有赖于低廉的保持一定浓度诱导物的存在,又必须清除分解代谢产物对酶合成的阻遏,其中的详细机制有待进一步的阐明。真菌纤维素酶的分泌也是相当复杂的,在酶的分泌过程中,酶会发生例如糖基化等一系列变化。提高纤维素酶的活力测定方法的准确性,使其进一步规范化,是研究纤维素酶工作的另外一个重要的领域。随着现代生物学朝着分子水平的不断发展,分子生物学的许多方法也越来越多地被应用于纤维素酶的研究中,并取得了重要进展。对真菌纤维素酶合成调节机制的深入研究,将为提高纤维素酶产量,推动应用工作的发展打下理论基础。     

接种固氮菌对纤维素分解过程的影响

从纤维素分解菌与联合固氮菌的接种配比,研究了混合培养对滤纸分解的影响。试验共设6个处理样,总接种量均为10%(V/V):处理Ⅰ,2%固氮菌+8%纤维素分解菌;处理Ⅱ,4%固氮菌+6%纤维素分解菌;处理Ⅲ,6%固氮菌+4%纤维素分解菌;处理Ⅳ,10%纤维素分解菌;处理Ⅴ,10%固氮菌;CK(空白对照)。结果显示:与处理Ⅳ相比,处理Ⅰ、Ⅱ的CMC酶活力及处理Ⅰ、Ⅱ、Ⅲ的滤纸分解率有明显提高。接种固氮菌的各处理样中,培养液中氮素含量与CK相比均有显著提高(P<0.05),且培养过程中pH值比较平稳,而未接种固氮菌处理培养液的氮素则低于CK,pH急剧降低。所有处理样中,接种2%固氮菌效果最佳,培养192h,其CMC酶活力与滤纸分解率比处理Ⅳ分别提高43.4%、240%;与处理Ⅴ相比,固氮菌数有显著增加(P<0.05),培养液中氮含量提高28.0%。     

Simultaneous hydrolysis and fermentation of pulp mill primary clarifier sludge

Bioconversion of sludge from the primary clarifier of a sulphite pulping operation to ethanol offers a number of advantages over conventional disposal options. The amount of material which must be disposed of is reduced while, at the same time, salable and environmentally friendly fuel-ethanol is produced. In this study, primary clarifier sludge (PCS) was shown to be hydrolysed to produce fermentable sugars at a rate proportional to enzyme loading. Initial (1 hour) hydrolysis rates as high as 12.6 g reducing sugar/L · h were observed at an initial enzyme loading of 10 filter paper units (FPU)/g. Hydrolysis was inhibited by spent sulphite liquor (SSL), an inhibition which could be completely overcome by fermenting the SSL to remove sugars. Surfactants were found to only marginally improve the production of sugars. To reduce the deleterious effects of end product inhibition, single stage simultaneous hydrolysis and fermentation (SHF) was carried out using cellulase enzymes and Saccharomyces cerevisiae.     

纤维素酶活性测定的生物传感器研究

用TiO2凝胶包埋葡萄糖氧化酶电化学传感器(GOD/TiO2)测定纤维素酶(CE)的活性,即基于电极对纤维素水解后生成葡萄糖的催化氧化。考察了各种实验条件对CE酶活性测定的影响。实验表明,GOD/TiO2电极检测电位为+0.50Vvs.SCE,稳态响应电流与纤维素酶活性在10～300U/L之间有线性关系,该方法可用于微量羧甲基纤维素酶活性测定。     

纤维素酶的固体发酵

从来自国内外11株菌株的初步比较,筛选出酶活较高的康氏木霉N_2—78和瑞热埃木霉QM6a。对康氏木霉P_2和土曲霉3.3935所作的纤维素碳源试验中,发现木质纤维素较纯纤维素好,未经处理的木质纤维素比经处理的好。麸皮和稀土对康氏木霉P_2产酶作用影响较大,而对土曲霉3.3935则无明显的影响。