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The Pol6 mutant of Penicillium occitanis, secreting a large quantity of cellulases, was cultivated in fermentor using a local paper pulp as an inducer substrate. A high titer of extracellular cellulase activity was reached after a fed batch process: 23 IU ml−1 filter paper activity, 21 IU ml−1 CMCases activity (endoglucanase units) and 25 mg ml−1 of proteins. Various tests were done to compare the action of the P. occitanis cellulases with those commercially available and with the traditional stonewashing process. This cellulase preparation was successfully applied in a biostoning process at an industrial scale. The abrasive effect of the P. occitanis cellulases was very uniform and with an efficiency comparable to that obtained by the commercial ones. 相似文献
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【目的】探讨绿色木霉分泌液能否分解小球藻细胞壁。【方法】用海藻酸钠和氯化钙固定绿色木霉,游离绿色木霉和固定化绿色木霉分别培养一段时间,离心培养液,用分光光度计法检测上清液中纤维素酶活性。在上清液中加入浓缩的小球藻悬浮液,用显微镜计数细胞壁破碎的小球藻。【结果】绿色木霉能同时分泌内切葡聚糖酶、外切葡聚糖酶及β-1,4葡萄糖苷酶3种纤维素酶,其中外切葡聚糖酶活性最高。固定化绿色木霉反复使用5次后,分泌的纤维素酶活性能保持到初次的67.4%。市售纤维素酶、游离绿色木霉、固定化绿色木霉初次及第5次分解小球藻细胞壁的效率分别为47.3%、86.5%、81.5%、52.1%。【结论】市售纤维素酶、游离绿色木霉、固定化绿色木霉都能分解小球藻细胞壁,其中固定化绿色木霉因可重复使用,具有潜在的应用前景。 相似文献
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In view of rising prices of crude oil due to increasing fuel demands, the need for alternative sources of bioenergy is expected
to increase sharply in the coming years. Among potential alternative bioenergy resources, lignocellulosics have been identified
as the prime source of biofuels and other value-added products. Lignocelluloses as agricultural, industrial and forest residuals
account for the majority of the total biomass present in the world. To initiate the production of industrially important products
from cellulosic biomass, bioconversion of the cellulosic components into fermentable sugars is necessary. A variety of microorganisms
including bacteria and fungi may have the ability to degrade the cellulosic biomass to glucose monomers. Bacterial cellulases
exist as discrete multi-enzyme complexes, called cellulosomes that consist of multiple subunits. Cellulolytic enzyme systems
from the filamentous fungi, especially Trichoderma reesei, contain two exoglucanases or cellobiohydrolases (CBH1 and CBH2), at least four endoglucanases (EG1, EG2, EG3, EG5), and
one β-glucosidase. These enzymes act synergistically to catalyse the hydrolysis of cellulose. Different physical parameters
such as pH, temperature, adsorption, chemical factors like nitrogen, phosphorus, presence of phenolic compounds and other
inhibitors can critically influence the bioconversion of lignocellulose. The production of cellulases by microbial cells is
governed by genetic and biochemical controls including induction, catabolite repression, or end product inhibition. Several
efforts have been made to increase the production of cellulases through strain improvement by mutagenesis. Various physical
and chemical methods have been used to develop bacterial and fungal strains producing higher amounts of cellulase, all with
limited success. Cellulosic bioconversion is a complex process and requires the synergistic action of the three enzymatic
components consisting of endoglucanases, exoglucanases and β-glucosidases. The co-cultivation of microbes in fermentation
can increase the quantity of the desirable components of the cellulase complex. An understanding of the molecular mechanism
leading to biodegradation of lignocelluloses and the development of the bioprocessing potential of cellulolytic microorganisms
might effectively be accomplished with recombinant DNA technology. For instance, cloning and sequencing of the various cellulolytic
genes could economize the cellulase production process. Apart from that, metabolic engineering and genomics approaches have
great potential for enhancing our understanding of the molecular mechanism of bioconversion of lignocelluloses to value added
economically significant products in the future.
JIMB 2008: BioEnergy - Special issue. 相似文献
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Due to the recent energy crisis and rising concern over climate change, the development of clean alternative energy sources is of significant interest. Biohydrogen produced from cellulosic feedstock, such as second generation feedstock (lignocellulosic biomass) and third generation feedstock (carbohydrate-rich microalgae), is a promising candidate as a clean, CO2-neutral, non-polluting and high efficiency energy carrier to meet the future needs. This article reviews state-of-the-art technology on lignocellulosic biohydrogen production in terms of feedstock pretreatment, saccharification strategy, and fermentation technology. Future developments of integrated biohydrogen processes leading to efficient waste reduction, low CO2 emission and high overall hydrogen yield is discussed. 相似文献
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Zvereva EA Fedorova TV Kevbrin VV Zhilina TN Rabinovich ML 《Extremophiles : life under extreme conditions》2006,10(1):53-60
Summary The cellulolytic activity of an alkaliphilic obligate anaerobic bacterium, Z-7026, which was isolated from the microbial community of soda-lake sediments and belongs to the cluster III of Clostridia with low G+C content, was studied. The bacterium was capable of growing in media with cellulose or cellobiose as the sole energy sources. Its maximal growth rate on cellobiose (0.042–0.046 h–1) was observed at an initial pH value of 8.5–9.0, whereas the maximal rate of cellulase synthesis, assayed by using a novel fluorimetric approach, was found to be 0.1 h–1 at pH 8–8.5. Secreted proteins revealed high affinity for cellulose and were represented by two major forms of molecular masses of 75 and 84 kDa, whereas the general protein composition of the precipitated and cellulose-bound preparations was similar to cellulosome subunits of Clostridium thermocellum. The optimum pH of the partially purified enzyme preparation towards both amorphous and crystalline cellulose was in the range 6–9, with more than 70% and less than 50% of maximal activity being retained at pH 9.2 and 5.0, respectively. 相似文献
7.
Enzymes and chelating agent in cotton pretreatment 总被引:6,自引:0,他引:6
Csiszár E Losonczi A Szakács G Rusznák I Bezúr L Reicher J 《Journal of biotechnology》2001,89(2-3):271-279
Desized cotton fabric and cotton seed-coat fragments (impurities) have been treated with commercial cellulase (Celluclast 1.5 L), hemicellulase–pectinase (Viscozyme 120 L) and xylanase (Pulpzyme HC) enzymes. Seed-coat fragments hydrolyzed much faster than the cotton fabric itself. This relative difference in hydrolysis rates makes possible a direct enzymatic removal of seed-coat fragments from desized cotton fabric. Addition of chelating agents such as ethylenediamine-tetra-acetic acid (EDTA) markedly enhanced the directed enzyme action. Pretreatments carried out in acidic solution at pH 5 increased the lightness of seed-coat fragments, contrary to the samples treated in neutral medium at pH 7. Alkaline scouring resulted in darker seed-coat fragments except for the samples pretreated with Pulpzyme HC plus EDTA. This effect is similar to that observed in the biobleaching process in pulp and paper industry. 相似文献
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Some authors have reported that as the applied agitation rate increases, the apparent activity of the endoglucanases from Trichoderma reesei towards cotton cellulose increases more markedly than does the apparent activity of the cellobiohydrolases. This suggests that the quality of cellulase finishing effects on cellulosic textiles may be machine-type dependent. The present work using total crude, endoglucanase-rich and cellobiohydrolase-rich cellulases from T. reesei confirmed that the final properties of woven, cotton fabrics treated under realistic processing conditions in a jet machine, were measurably and perceivably different from those of the same fabrics, treated using the same processing conditions of temperature, time, pH, enzyme concentration and fabric to liquor ratio, but in a winch machine. The results are interpreted in terms of the effects of agitation rate on the adsorption–desorption behaviour of the T. reesei endoglucanases and cellobiohydrolases. 相似文献
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Direct utilization of untreated oil palm trunk (OPT) for cellulases and xylanase production by Aspergillus fumigatus SK1 was conducted under solid-state fermentation (SSF). The highest activities of extracellular cellulases and xylanases were produced at 80% moisture level, initial pH 5.0, 1 × 108 spore/g (inoculum) with 125 μm of OPT as sole carbon source. The cellulases and xylanase activities obtained were 54.27, 3.36, 4.54 and 418.70 U/g substrates for endoglucanase (CMCase), exoglucanase (FPase), β-glucosidase and xylanase respectively. The crude cellulases and xylanase required acidic condition to retain their optimum activities (pH 4.0). Crude cellulases and xylanase were more stable at 40 °C compared to their optimum activities conditions (60 °C for FPase and 70 °C for CMCase, β-glucosidase and xylanase). SDS-PAGE and zymogram analysis showed that Aspergillus fumigatus SK1 could secrete cellulases (endoglucanase, exoglucanase and β-glucosidase), xylanase and protease. Enzymatic degradation of alkaline treated OPT with concentrated crude cellulases and xylanases resulted in producing polyoses. 相似文献