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排序方式: 共有933条查询结果,搜索用时 15 毫秒
21.
Katrin Greimel Annemarie Marold Christian Sohar Roland Feola Armin Temel Thomas Schoenbacher Enrique Herrero Acero Georg M. Guebitz 《Reactive and Functional Polymers》2013,73(10):1335-1339
The potential of two hydrolytic enzymes, namely a lipase from Thermomyces lanuginosus (TlL) and a cutinase from Humicola insolens (HiC) for hydrolysis of the phthalic acid backbone based polyester coatings was assessed. Two phthalic acid/trimethylolpropane based model substrates resembling the structure of the polyester backbone of coatings were synthesized. Out of both enzymes, only the cutinase was able to hydrolyze both model substrates while the larger substrate was hydrolyzed at a lower rate. The cutinase was also able to hydrolyze a coating (alkyd resin) both in suspension and as dried film. LC–MS analysis of the hydrolysis products released from the coating revealed the presence of oleic acid, its monoglyceride, phthalic acid and 2-((3-((2-((2,3-dihydroxypropoxy)carbonyl)benzoyl)oxy)-2-hydroxypropoxy)carbonyl)benzoic acid. These results indicate that the enzyme was able to hydrolyze the polyester backbone as well as to release fatty acid side chains. Consequently, enzymatic hydrolysis has a potential for the removal of coatings, their recycling or their functionalization. 相似文献
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γ-癸内酯的酶法拆分研究 总被引:2,自引:0,他引:2
研究了脂肪酶对γ-癸内酯(GDL)对映催化选择性水解反应,考察了各种因素对酶促水解拆分过程的影响。试验结果表明,水解产物-大量的酸会抑制脂肪酶的活性,采用高浓度的磷酸盐缓冲液可有效地稳定系统的酸碱度,使酶促反应顺利进行。在磷酸缓冲溶液体系中缓冲液pH=7.8,底物浓度为0.6mol/L,反应时间2.5小时,反应温度43℃为γ-癸内酯酶促水解拆分的最佳工艺条件。 相似文献
24.
Anders?Falk?VikbjergEmail author Lifeng?Peng Huiling?Mu Xuebing?Xu 《Journal of the American Oil Chemists' Society》2005,82(4):237-242
The possibilities of producing structured phospholipids between soybean phospholipids and caprylic acid by lipase-catalyzed
acidolysis were examined in continuous packedbed enzyme reactors. Acidolysis reactions were performed in both a solvent system
and a solvent-free system with the commercially immobilized lipase from Thermomyces lanuginosa (Lipozyme TL IM) as catalyst. In the packed bed reactors, different parameters for the lipase-catalyzed acidolysis were elucidated,
such as solvent ratio (solvent system), temperature, substrate ratio, residence time, water content, and operation stability.
The water content was observed to be very crucial for the acidolysis reaction in packed bed reactors. If no water was added
to the substrate during reactions under the solvent-free system, very low incorporation corporation of caprylic acid was observed.
In both solvent and solvent-free systems, acyl incorporation was favored by a high substrate ratio between acyl donor and
phospholipids, a longer residence time, and a higher reaction temperature. Under certain conditions, the incorporation of
around 30% caprylic acid can be obtained in continuous operation with hexane as the solvent.
Presented at the 95th American Oil Chemists' Society Annual Meeting and Expo in Cincinnati, Ohio, May 10, 2004. 相似文献
25.
With the rapid increase of lubricant consumption,oil contamination becomes more serious.Biotreatment is an important method to remove oil contamination with some advantages.In this study,acclimatized oilcontaminated soil and used lubricating oil were sampled to isolate lubricant-degrading strains by several methods.51 isolates were obtained and 24-well plates were employed to assess bacterial potential in highthroughput screening.The method was noted for the prominence of oil–water two-phase system with saving chemicals,shortening cycles and lessening workloads.In order to decrease inaccuracy,subculture and resting cells were inoculated into mineral salt medium with 200 μl oil in well plates for the cultivation at 37 °C for 5and 7 days,and the biodegradation potential was characterized by the changes of oil film and cell density.With appropriate evaluation by shaking flask tests,5 isolates were retained for their potentials with the maximum biodegradation from 1500 to 2200 mg · L~(-1)and identified as Acidovorax citrulli,Pseudomonas balearica,Acinetobacter johnsonii(two isolates with different biodegradation potentials)and Acidovorax avenae using 16 S r RNA sequencing analysis.Also,lipase activity was determined using indicator titration and p-nitrophenyl palmitate(p-NPP)methods.The results indicated that only p-NPP was successful to test lipase activity with the range of 1.93–6.29 U · ml~(-1).Although these five strains could degrade 1000 mg · L~(-1)lubricating oil in158–168 h,there existed distinct difference in enzyme activity,which demonstrates that lipase activity could not be used as the criterion to evaluate microbial biodegradation potential for petroleum hydrocarbons. 相似文献
26.
For the efficient conversion of L-tyrosine(L-Tyr) to tyrosol, which is an aromatic compound widely used in the pharmaceutical and chemical industries, a novel four-enzyme cascade pathway based on the Ehrlich pathway of Saccharomyces cerevisiae was designed and reconstructed in Escherichia coli. Then,the expression levels of the relevant enzymes were coordinated using a modular approach and gene duplication after the identification of the pyruvate decarboxylase from Candida tropicalis(Ct PDC) as ... 相似文献
27.
讨论了淀粉、粗玉米粉及可以被淀粉所依附的纤维素框架的化学结构及性质,它们可能成为一系列用途广泛的干燥剂。 相似文献
28.
29.
Louw TM Booth CS Pienaar E Termaat JR Whitney SE Viljoen HJ 《Chemical engineering science》2011,(8):1783-1789
Recently a theoretical analysis of PCR efficiency has been published by Booth et al. (2010). The PCR yield is the product of three efficiencies: (i) the annealing efficiency is the fraction of templates that form binary complexes with primers during annealing, (ii) the polymerase binding efficiency is the fraction of binary complexes that bind to polymerase to form ternary complexes and (iii) the elongation efficiency is the fraction of ternary complexes that extend fully. Yield is controlled by the smallest of the three efficiencies and control could shift from one type of efficiency to another over the course of a PCR experiment. Experiments have been designed that are specifically controlled by each one of the efficiencies and the results are consistent with the mathematical model. The experimental data has also been used to quantify six key parameters of the theoretical model. An important application of the fully characterized model is to calculate initial template concentration from real-time PCR data. Given the PCR protocol, the midpoint cycle number (where the template concentration is half that of the final concentration) can be theoretically determined and graphed for a variety of initial DNA concentrations. Real-time results can be used to calculate the midpoint cycle number and consequently the initial DNA concentration, using this graph. The application becomes particularly simple if a conservative PCR protocol is followed where only the annealing efficiency is controlling. 相似文献
30.
The production of sterol ester by transesterification of β‐sitosterol with fish oil (TAG) catalyzed by Thermomyces lanuginosus immobilized lipase enzyme with varied reaction parameters such as temperature, substrate molar ratio, concentration of enzyme to deduce the enzyme kinetics for the reaction was investigated. For this transesterification reaction, the kinetic model was derived by using Ping Pong Bi Bi Mechanism. The Km value from the first plot containing fish oil as substrate was 1.31 ± 0.05, while Km from the second plot containing β‐sitosterol as substrate was 1.01 ± 0.04; identical Vmax (0.213 ± 0.06) values were obtained by keeping one of the substrate concentration constant and varying the other. Practical applications : Deduction of reaction kinetics is an important criterion to ascertain the viability of any chemical process. Enzymatic processes need special attention to set model reaction parameters which could help in optimization or design of the actual process. In the present study we have derived the enzyme kinetics for the production sterol ester, an important nutraceutical, and calculated its Km and Vmax values along with the Arhenius activation energy to establish the viability of the reaction. 相似文献