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斯达氏油脂酵母利用混合糖发酵产油脂 总被引:11,自引:0,他引:11
研究了斯达氏油脂酵母Lipomyces starkeyi2#利用葡萄糖-木糖混合糖为碳源生长和油脂积累特性。L.star-keyi2#利用70 g/L葡萄糖和70 g/L木糖作为碳源在30℃下摇瓶发酵96 h,糖利用率均达90%以上,菌体生物量分别为14.1 g/L和13.1 g/L,油脂质量分数分别为55.7%和52.6%。相同条件下该菌株利用混合糖(葡萄糖46 g/L,木糖24 g/L)为碳源时总糖利用率、生物量和油脂质量分数分别为75.1%,15.0 g/L和40.0%。借助于P lackett-Burm an设计法和单因子实验法对培养条件进行了优化,结果表明发酵96 h混合糖利用率可达到97.3%,发酵120 h后混合糖利用率、生物量和菌体油脂质量分数分别达99.5%、19.0 g/L和52.6%。生物量得率和油脂得率分别达到27%和14%。 相似文献
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摘要:目的 微生物油脂可作为制备绿色能源生物柴油的原料。对酵母微生物油脂的生物合成方法进行研究。方法 以斯达油脂酵母Lipomyces starkeyi AS 2.1560为菌种进行微生物油脂生物合成。首先获得大量细胞,将细胞收集后,转移至葡萄糖溶液中进行油脂合成。结果 斯达油脂酵母可在不含有其他营养成分的葡萄糖溶液中快速合成油脂,细胞油脂含量可达到细胞干重的60%以上。菌龄对油脂生成影响不明显,糖浓度过高抑制油脂生成,40 g/L葡萄糖溶液中60 h合成油脂最多,达到65.2%,并有进一步积累的可能,在(0.5~6)×108个/mL,接种细胞的密度越大,油脂合成能力越低。合成油脂成分主要为棕榈酸和油酸。结论 斯达油脂酵母细胞增殖与油脂生物合成可分开进行,其油脂成分与普通动植物油脂成分相似。 相似文献
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皮状丝孢酵母B3利用木薯淀粉发酵生产微生物油脂 总被引:3,自引:1,他引:2
对皮状丝孢酵母B3以木薯淀粉水解液为碳源发酵生产微生物油脂培养条件进行了优化,并在2 L发酵罐中对菌体生长和油脂积累进行了考察。摇瓶实验表明,木薯淀粉水解液的浓度高于90 g/L时不利于菌体的生长和油脂积累,皮状丝孢酵母B3发酵生产微生物油脂的最适氮源及其浓度、最适C/N比和pH分别为酵母提取物3.0 g/L、116、6.0,在此条件下培养144 h菌体生物量、油脂产量和油脂含量分别达到15.2 g/L、6.22 g/L和40.9%;在2 L发酵罐中分批发酵44 h后菌体生物量、油脂产量和油脂含量分别达28.7 g/L、12.27 g/L和42.8%。以皮状丝孢酵母B3所产油脂制备生物柴油,其主要组成包括棕榈酸甲酯、硬脂酸甲酯、油酸甲酯、亚油酸甲酯等,且理化特性符合相关国家标准,可作为一种有潜力的化石燃料替代品。 相似文献
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异养细胞种子/光自养培养方法是一种可异养培养的能源微藻培养的有效方法,但已有文献尚未从工艺优化角度考察其发展潜力。为了获得较高细胞密度的用于光自养培养的种子和提高光自养培养的细胞密度与油脂产率,对异养细胞种子/光自养培养的培养基和培养条件进行了优化。结果表明,采用优化后的培养基,椭圆小球藻在摇瓶中异养培养的最高藻细胞密度可达11.04 g/L,比在初始培养基条件下提高了28.0%,在5 L发酵罐中异养培养的藻细胞密度达到73.89 g/L;在2 L柱式光生物反应器中光自养培养的藻细胞密度、油脂含量和油脂产率分别达1.62 g/L、36.34%和6.1 mg/(L·h),油脂成分主要为含C16-C18碳链的脂肪酸,是制备生物柴油的理想原料。经过优化,异养细胞种子/光自养培养这一方法能够显著地提高椭圆小球藻产油脂的能力,这进一步表明异养细胞种子/光自养培养方法有望成为可异养的能源微藻的高效培养方式。 相似文献
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以毕赤酵母发酵废液为水源并提供部分C源和N、P,在500 mL摇瓶中,比较了发酵废液培养基与SE基础培养基对原始小球藻的生长影响,并通过单因素和正交优化发酵废液培养基。结果表明,发酵废液培养基适合于原始小球藻的培养。利用发酵废液培养小球藻,在添加葡萄糖0.05 mol/L,硝酸钠0.01 mol/L,磷酸二氢钾0.003 mol/L,海绿素浓度300μL/L,培养7 d后最高生物量达6.56 g/L,油脂含量达33.68%,两者均高于SE基础培养基。油脂的脂肪酸组成分析表明,废液培养基培养下小球藻油脂的脂肪酸组成主要是C16∶0(25.12%)、C18∶0(4.69%)、C18∶1(50.46%)、C18∶2(6.78%)、C18∶3(8.58%),而SE培养基培养的小球藻油脂脂肪酸组成主要是C16∶0(24.56%)、C18∶0(20.36%)、C18∶1(16.66%)、C18∶2(14.32%)、C18∶3(30.98%),两种培养基培养所得藻油脂肪酸组成虽相差较大,但均适合作为生物柴油的原料。 相似文献
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圆红冬孢酵母两阶段培养法生产微生物油脂 总被引:5,自引:2,他引:5
为缩短发酵时间,减少原料消耗,采用细胞增殖和油脂积累分离的两阶段模式,培养圆红冬孢酵母Rhodosporidium toruloides AS 2.1389生产微生物油脂。结果表明,细胞增殖阶段获得的R.toruloides AS 2.1389细胞,重悬接种在葡萄糖溶液中,可快速积累油脂,菌体油脂含量超过自身干重的55%。增殖阶段细胞的菌龄越高,产油能力越强。油脂积累阶段使用高浓度葡萄糖溶液或未灭菌的葡萄糖溶液,油脂合成可以有效进行。油脂中脂肪酸成分以含16和18个碳原子的长链脂肪酸为主,可作为制备生物柴油的新型原料。 相似文献
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为了探究纤维素水解液中常见的发酵抑制物糠醛对粘红酵母Rhodotorula glutinis生长与油脂积累的影响,对比了不同的糠醛浓度(0.1、0.4、0.6、1.5 g/L)下粘红酵母的生物量和油脂积累情况,并探究了1.0 g/L的糠醛对粘红酵母不同碳源(葡萄糖和木糖)利用的影响。研究表明,当糠醛浓度达1.5 g/L时,粘红酵母的延迟期延长至96 h,残糖高达17.7 g/L,生物量最高6.6 g/L,仅为正常积累量的47%,油脂含量也减少了约50%;以木糖为碳源时,糠醛对粘红酵母的抑制程度小于葡萄糖为碳源时的情况;在糠醛存在的逆境中,粘红酵母倾向于生成更多的18碳脂肪酸或18碳不饱和脂肪酸。 相似文献
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Abstract. The influence of glucose, fructose and sucrose on oviposition site selection by Lobesia botrana is studied by combining behavioural and electrophysiological experiments. Oviposition choice assays, using surrogate grapes treated with grape berry surface extracts of Vitis vinifera cv. Merlot at different development stages, show that L. botrana females are most stimulated by extracts of mature berries containing the highest concentrations of glucose and fructose. Choice assays reveal that the oviposition response to these sugars is dose-dependant (with a threshold of the applied solution = 10 m m and a maximum stimulation at 1 m ) and that females are more sensitive to fructose than to glucose. Tarsal contact-chemoreceptor sensilla are unresponsive to stimulation with sugars but the ovipositor sensilla contain at least one neurone most sensitive to fructose and sucrose with a threshold of approximately 0.5 m m . Corresponding to the behavioural data, glucose is significantly less stimulatory to sensilla than fructose or sucrose. It is argued that fructose may be of special importance for herbivorous insects exploiting fruit as an oviposition site. 相似文献
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Log colonization by Ips sexdentatus prevented by increasing host unsuitability signaled by verbenone
Iñaki Etxebeste Gonzalo Álvarez Juan Pajares 《Entomologia Experimentalis et Applicata》2013,147(3):231-240
Sudden increments of breeding material after windstorms, forest fires, or inappropriate management practices help bark beetles such as Ips sexdentatus Boerner (Coleoptera: Curculionidae: Scolytinae) increase in numbers and colonize standing healthy pine trees. Preventing bark beetles from arriving to susceptible trees or logs may have great relevance for bark beetle management. Recent studies have reported inhibition of the aggregation response of I. sexdentatus using verbenone. Two field experiments were conducted to examine the effect of verbenone on the colonization pattern of this beetle. The first experiment tested the combined effect of trans‐conophthorin, a non‐host bark volatile with known repellent effect, and verbenone on Pinus sylvestris L. (Pinaceae) log piles of two sizes, but failed to protect them against I. sexdentatus attack when these two infochemicals were released at low rates. The results of this experiment suggested an interaction with the associated secondary bark beetle Orthotomicus erosus (Wollaston). A second experiment examined the response of I. sexdentatus and O. erosus to log piles that released verbenone at 0, 2, 10, or 40 mg day?1. Although I. sexdentatus colonization of Pinus nigra Arnold logs was completely prevented at 40 mg day?1, O. erosus could be found at all tested verbenone release rates. Besides verbenone, O. erosus colonization density and the height from which logs originated were the variables that best explained I. sexdentatus log colonization pattern. In addition, I. sexdentatus and O. erosus were rarely recorded colonizing the same log, and niche breadth analyses suggested that they excluded each other. The role of verbenone in the colonization process and its potential use in the prevention of population buildups of damaging bark beetles such as I. sexdentatus are discussed. 相似文献
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Weis RM 《Nature structural & molecular biology》2006,13(5):382-384
Bacterial chemotaxis systems have cooperatively interacting clusters of transmembrane receptors and signaling proteins to detect, amplify, integrate and adapt to environmental signals. A recent study provides experimental data to construct a new model of the signaling complex. 相似文献
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Mitsuhiko Satô 《Phytochemistry》1980,19(9):1931-1933
The activity of spinach chloroplast phenolase which had been repressed by ammonium oxalate was restored by adding copper. Oxalate appears to bind to the enzyme at a single site, the binding paralleling the inhibition produced at neutral pH. The inhibition of oxalate is due to its binding with copper at the active centre to form an inactive complex, the oxalate moiety of which is releasable when more copper is added. Similar reactivation by copper was obtained with pure mushroom phenolase. 相似文献
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The biodegradation of anthracene-9, 10-diethanol by the ligninolytic fungus Phanerochaete chrysosporium, previously though to involve singlet oxygen, is shown to be catalyzed by lignin peroxidases. Veratryl alcohol stimulated the enzymatic degradation of anthracenediethanol, and anthracenediethanol inhibited enzymatic oxidation of veratryl alcohol. Competition for oxidation by lignin peroxidase is suggested as the mechanism of the inhibition of lignin biodegradation by anthracenediethanol and related anthracene derivatives.Abbreviations ADE
anthracene-9,10-diethanol
- AES
anthracene-9,10-bisethanesulfonic acid
- DHP
dehydrogenative polymerizate
- DMF
N,N-dimethylformamide
- EPX
9,10-endoperoxide of ADE
- PMR
proton magnetic resonance 相似文献
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Bhide VM Laschinger CA Arora PD Lee W Hakkinen L Larjava H Sodek J McCulloch CA 《The Journal of biological chemistry》2005,280(24):23103-23113
Decorin is a small, leucine-rich proteoglycan that binds to collagen and regulates fibrillogenesis. We hypothesized that decorin binding to collagen inhibits phagocytosis of collagen fibrils. To determine the effects of decorin on collagen degradation, we analyzed phagocytosis of collagen and collagen/decorin-coated fluorescent beads by Rat-2 and gingival fibroblasts. Collagen beads bound to gingival cells by alpha2beta1 integrins. Binding and internalization of decorin/collagen-coated beads decreased dose-dependently with increasing decorin concentration (p < 0.001). Inhibition of binding was sustained over 5 h (p < 0.001) and was attributed to interactions between decorin and collagen and not to decorin-collagen receptor interactions. Both the non-glycosylated decorin core protein and the thermally denatured decorin significantly inhibited collagen bead binding (approximately 50 and 89%, respectively; p < 0.05). Mimetic peptides corresponding to leucine-rich repeats 1-3, encompassed by a collagen-binding approximately 11-kDa cyanogen bromide fragment of decorin and leucine-rich repeats 4 and 5, previously shown to bind to collagen, were tested for their ability to inhibit collagen bead binding. Although the synthetic peptide 3 alone exhibited saturable binding to collagen, neither peptides 3 nor 1 and 2 markedly inhibited phagocytosis. Leucine-rich repeat 3 bound to a triple helical peptide containing the alpha2 integrin-binding site of collagen. When collagen beads were co-incubated with peptides 3 and 4, inhibition of collagen phagocytosis (55%) was equivalent to intact native/recombinant core protein. Thus a novel collagen binding domain in decorin acts cooperatively with leucine-rich repeat 4 to mask the alpha2beta1 integrin-binding site on collagen, an important sequence for the phagocytosis of collagen fibrils. 相似文献
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In this study we have explored the behaviour of peptides after capillary electrophoresis (CE) followed by elution under pressure. The use of D2O- rather than H2O-based buffer solutions appears to restrict the diffusion of peptides after CE, resulting in little loss of resolution when peptides are eluted by dynamic flow. In this paper we present results showing that a simple two-step process, involving CE at a low voltage, switching off the power supply, and connecting the fused capillary at the anode end to a syringe pump for dynamic flow, can retain separation characteristics and can be used for the isolation of picomole quantities of peptides for sequence determination. 相似文献
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