共查询到20条相似文献,搜索用时 437 毫秒
1.
W. F. Hu S. N. Sin H. Chua P. H. F. Yu 《Applied biochemistry and biotechnology》2005,121(1-3):289-301
Accumulation of poly hydroxyalkanoate (PHA) from excess activated sludge (EAS) was monitored and controlled via the oxidation-reduction
potential (ORP) adjusting process. The ORP was adjusted and controlled by only regulating the gas-flow rate pumped into the
cultural broth in which sodium acetate (C2) and propionate (C3) were used as carbon sources. Productivity of PHA and the PHA
compositions at various C2 to C3 ratios were also investigated. When ORP was maintained at +30 mV, 35% (w/w) of PHA of cell
dry weight obtained when C2 was used as sole carbon source. The PHA copolymer, poly-(3-hydroxybutyrate-co-3-hydroxyvalerate)
(PHBV), accumulated by EAS with different 3-hydroxyvalarate (3HV) molar fractions ranged from 8% to 78.0% when C2 and C3 was
used as sole carbon source, By using ORP to monitor and control the fermentation process instead DO meter, the ORP system
provided more precise control to the PHA accumulation process from EAS under low dissolved oxygen (DO) concentrations. Adjusting
the C2 to C3 ratios in the media could control the composition such as the 3HV/3HB ratios of the PHBV. Furthermore, it might
be an effective way to adjust the 3HV molar fractions in PHBV by controlling the DO concentration via the ORP monitoring system.
The 3HV molar fractions in the PHBV declined with increasing ORP from −30 mV to +100 mV by adjusting the gas-flow rate (i.e.
the DO concentration). It is concluded that the DO plays a very important role in the synthesis of 3HV subunits in PHBV co-polymer
from the EAS. Therefore, a hypothetic metabolic model for PHA synthesis from EAS was proposed to try to explain the results
in this study. 相似文献
2.
Tsuge T Yano K Imazu S Numata K Kikkawa Y Abe H Taguchi S Doi Y 《Macromolecular bioscience》2005,5(2):112-117
Eleven laboratory-evolved polyhydroxyalkanoate (PHA) synthases which originated from Pseudomonas sp. 61-3 enzyme (PhaC1(Ps)), together with the wild-type enzyme, were applied for PHA synthesis from fructose using Ralstonia eutropha PHB(-)4 as a host strain. The evolved PhaC1(Ps) mutants had amino acid substitution(s) at position 325 and/or position 481. In these mutants, serine-325 (S325) was replaced by cysteine (C) or threonine (T), while glutamine-481 (Q481) was replaced by lysine (K), methionine (M) or arginine (R). All recombinant strains harboring the genes of the evolved PhaC1(Ps) mutants produced a significantly increased amount of PHA (55-68 wt.-%) compared with the one harboring the wild-type gene (49 wt.-%). Particularly, those evolved PhaC1(Ps) mutants having multiple amino acid substitutions showed higher activities for PHA synthesis. Characterization of the PHA by NMR spectroscopy revealed that they were copolymers consisting of (R)-3-hydroxybutyrate (98-99 mol-%) and medium-chain-length comonomers (1-2 mol-%). This study also confirmed that amino acid substitution at position 481 in PhaC1(Ps) led to an increasing molecular weight of PHA. The number-average molecular weight (Mn) of PHA (Mn = 240,000) synthesized by the evolved PhaC1(Ps) (Q481K) mutant was 4.6-fold greater than that (Mn = 52,000) synthesized by the wild-type enzyme. 相似文献
3.
Qun Yan Chung Him Yu Peter Hoi Fu Yu Hua Zou Wen-quan Ruan 《高分子科学》2007,(4):341-345
Biosynthesis and thermal properties of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) with different HV (hydrovalerate) content produced by a Bacillus cereus strain were investigated. A large variety of HV contents (up to about 90 mol%) of PHBV could be produced by this strain. Combined nitrogen sources containing both yeast extract and ammonium sulphate were better for cell growth and polyhydroxyalkanoates (PHA) production than either yeast extract or ammonium sulphate alone. Propionic acid is more favorable for the production of HV content than that of valeric acid. Finally, thermal properties of PHBV produced by this strain are found close to the results of other groups. 相似文献
4.
核壳结构葡萄糖敏感微凝胶的制备 总被引:1,自引:0,他引:1
用先合成聚N-异丙基丙烯酰胺(PNIPAM)微凝胶核再包一层N-异丙基丙烯酰胺/丙烯酸共聚物(P(NIPAM-co-AA))壳的办法合成了一系列核壳结构微凝胶.微凝胶壳层厚度随投入的壳储备溶液的增加而增加.研究了pH=3.5时核壳微凝胶的温敏体积相转变行为.由于PNIPAM核和P(NIPAM-co-AA)壳的相转变温度很接近,因此只观察到一个相转变.在EDC催化下使3-氨基苯硼酸与壳层中的羧基反应,将苯硼酸基(PBA)引入微凝胶,得到核为PNIPAM、壳为P(NIPAM-co-AMPBA)的核壳结构微凝胶.改性后的微凝胶表现出3个体积相转变过程.其中第一个对应于P(NIPAM-co-AMPBA)壳层的体积相转变.第二和第三个则是PNIPAM核的相转变过程.由于在沉淀聚合时交联剂BIS反应性更大,PNIPAM核结构不均一,形成BIS含量高的"核"和BIS含量低的"壳".BIS含量低的"壳"被一层疏水的P(NIPAM-co-AMPBA)壳包裹,拉大了其与"核"的相转变温度的差别,因此随着温度升高表现出两个相转变过程.PBA改性的微凝胶同样表现出葡萄糖敏感性,但在葡萄糖存在下溶胀度的改变较小. 相似文献
5.
Tsuge T Saito Y Narike M Muneta K Normi YM Kikkawa Y Hiraishi T Doi Y 《Macromolecular bioscience》2004,4(10):963-970
Type I polyhydroxyalkanoate (PHA) synthases, as represented by Ralstonia eutropha enzyme (PhaC(Re)), have narrow substrate specificity toward (R)-3-hydroxyacyl-coenzyme A with acyl chain length of C3-C5 to yield PHA polyesters. In this study, saturation point mutagenesis of a highly conserved alanine at position 510 (A510) in PhaC(Re) was carried out to investigate the effects on the polymerization activity and the substrate specificity for in vivo PHA biosynthesis in bacterial cells. A series of saturation mutants were first applied for poly[(R)-3-hydroxybutyrate] homopolymer synthesis in Escherichia coli and R. eutropha PHB(-)4 (PHA negative mutant) cells to assess the polymerization activity. All mutants showed quantitatively similar polymerization activities when R. eutropha PHB(-)4 was used for assay, whereas several mutants such as A510P showed low activities in E. coli. Further analysis has revealed that majority of mutants synthesize polyesters with higher molecular weights than the wild-type. In particular, substitution by acidic amino acids, A510D(E), led to remarkable increases in molecular weights. Subsequently, PHA copolymer synthesis from dodecanoate (C12 fatty acid) was examined. The copolymer compositions were varied depending on the mutants used. Significant increased fractions of long monomer units (C6 and C8) in PHA copolymers were observed for three mutants [A510M(Q,C)]. From these results, the mutations at this potion are beneficial to change the molecular weight of polyesters and the substrate specificity of PhaC(Re). Molecular weight distributions of PHA polymers synthesized by the wild-type enzyme (PhaC(Re)) and its mutants. 相似文献
6.
Tsuge T Watanabe S Sato S Hiraishi T Abe H Doi Y Taguchi S 《Macromolecular bioscience》2007,7(6):846-854
Amino acid substitutions at two residues downstream from the active-site histidine of polyhydroxyalkanoate (PHA) synthases are effective for changing the composition and the molecular weight of PHA. In this study, saturation mutagenesis at the position Ala505 was applied to PHA synthase (PhaCAc) from Aeromonas caviae to investigate the effects on the composition and the molecular weight of PHA synthesized in Ralstonia eutropha. The copolymer composition and molecular weight of PHA were varied by association with amino acid substitutions. There was a strong relationship between copolymer composition and PHA synthase activity of the cells. This finding will serve as a rationale for producing tailor-made PHAs. 相似文献
7.
Anatoly N. Boyandin Valentin P. Rudnev Vladimir N. Ivonin Svetlana V. Prudnikova Ksenia I. Korobikhina Maxim L. Filipenko Tatiana G. Volova Anthony J. Sinskey 《Macromolecular Symposia》2012,320(1):38-42
Summary: Biodegradation of film specimens from polyhydroxyalkanoates (PHAs) of two types – poly-3-hydroxybutyrate (PHB) and poly-3-hydroxybutyrate-co-3-hydroxyvalerate (PHBV) – was analysed in different environments: tropical sea waters of the South China Sea (Nha Trang, Vietnam) and soils in the environs of Hanoi (Vietnam), Nha Trang (Vietnam) and Krasnoyarsk (Siberia, Russia). In seawater, the mass loss of the specimens of both types was almost equal. However, in tropical soils, PHB degraded quicker than PHBV. In the Siberian soil, the degradation rate of the PHBV was generally higher than that of PHBV. Analysis of molecular mass of PHA specimens showed its decreasing during biodegradation. In the tropical sea conditions, PHA degrading microorganisms were represented by bacteria of Enterobacter, Bacillus and Gracilibacillus genera. Among PHA degrading bacteria, Burkholderia, Alcaligenes, Bacillus, Mycobacterium and Streptomyces genera were identified in Vietnamese soils, and Variovorax, Stenotrophomonas, Acinetobacter, Pseudomonas, Bacillus and Xanthomonas genera in Siberian soils. Micromycetes of Gongronella, Paecilomyces, Penicillium and Trichoderma genera exhibited PHA degrading activity in Vietnamese soils, and Paecilomyces, Penicillium, Acremonium, Verticillium and Zygosporium genera – in Siberian soils. 相似文献
8.
WANG Yan LI Fan WANG Zhan-yong LIU Dong-bo XIA Hong-mei LIU Ling-fei CHEN Shan 《高等学校化学研究》2012,28(3):459-464
An extracellular polyhydroxybutyrate(PHB) depolymerase was purified to homogeneity from the culture supernatant of a PHB-degrading bacterium, Pseudomonas mendocina DSWY0601, which was isolated from brewery sewage for the ability to form clear zones on the PHB mineral agar plates. The molecular weight of the purified PHB depolymerase as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis(SDS-PAGE) was approximately 59800 at the optimal temperature and pH value being 50 ℃ and 8.5, respectively. PHB depolymerase was stable in a temperature range of 20―50 ℃ and sensitive to pH value within a pH range of 8.0―9.5. PHB depolymerase degraded poly-3-hydroxybutyrate-co-4-hydroxybutyrate(P3/4HB) and poly-3-hydroxybutyrate-co-3- hydroxyvalerate(PHBV) but did not degrade poly(lactic acid)(PLA), poly(butylene succinate)(PBS) or poly- (caprolactone)(PCL). PHB depolymerase was sensitive to phenylmethylsulfonyl fluoride(PMSF), H2O2 and SDS. The main product after enzymatic degradation of PHB was indentified as 3-hydroxbutyrate monomer(3HB) by mass spectrometric analysis, suggesting that PHB depolymerase acted as an exo-type hydrolase. Analysis of phaZpm gene reveals that PHB depolymerase is a typical denatured short-chain-length PHA(dPHASCL, PHA=polyhydroxyalkanoate) depolymerase containing catalytic domain, linker and substrate-binding domain. 相似文献
9.
In this study, activated sludge bacteria from a conventional wastewater treatment process were induced to accumulate polyhydroxyalkanoates
(PHAs) under different carbon-nitrogen (C:N) ratios. As the C:N ratio increased from 20 to 140, specific polymer yield increased
to a maximum of 0.38 g of polymer/g of dry cell mass while specific growth yield decreased. The highest overall polymer production
yield of 0.11 g of polymer/g of carbonaceous substrate consumed was achieved using a C:N ratio of 100. Moreover, the composition
of polymer accumulated was dependent on the valeric acid content in the feed. Copolymer poly (3-hydroxybutyrate-co-3-hydroxyvalerate)
[P(3HB-co-3HV)] was produced in the presence of valeric acid. The 3-hydroxyvalerate (3HV) mole fraction in the copolymer was
linearly related tovaleric content in the feed, which reached a maximum of 54% when valeric acid was used as sole carbon source.
When the 3HV U in the polymer increased from 0–54 mol%, the melting temperature decreased from 178° to 99°C. Thus, the composition,
and hence the mechanical properties, of the copolymer produced from activated sludge can be controlled by adjusting the mole
fraction of valeric acid in the feed medium. 相似文献
10.
以水热合成法制备的一维取向n型ZnO纳米线阵列为衬底,采用电化学沉积法在其上沉积生长一层p型Cu2O半导体包覆层,制备出了新型ZnO/Cu2O异质结纳米线阵列光敏器件.利用XRD、SEM、TEM、XPS、PL及光响应特性等测试方法对样品的形貌、晶体结构、化学成分及光电特性进行了分析表征.研究了生长条件对ZnO/Cu2O异质结纳米线阵列各种特性的影响.研究发现,适宜的沉积电压和沉积时间是保证ZnO/Cu2O异质结光敏器件具有适宜厚度核壳包覆层及较好光响应特性的关键因素.研究结果为ZnO及Cu2O半导体材料在光敏器件中的应用提供了实验基础. 相似文献
11.
Three different microbial wild-type strains are compared with respect to their potential as industrial scale polyhydroxyalkanoate (PHA) producers from the feed stock whey lactose. The halophilic archaeon Haloferax mediterranei as well as two eubacterial strains (Pseudomonas hydrogenovora and Hydrogenophaga pseudoflava) are investigated. H. mediterranei accumulated 50 wt.-% of poly-3-(hydroxybutyrate-co-8%-hydroxyvalerate) from hydrolyzed whey without addition of 3-hydroxyvalerate (3HV) precursors (specific productivity q(p): 9.1 mg x g(-1) x h(-1)). Using P. hydrogenovora, the final percentage of poly-3-hydroxybutyrate (PHB) amounted to 12 wt.-% (q(p): 2.9 mg x g(-1) x h(-1)). With H. pseudoflava, it was possible to reach 40 wt.-% P-3(HB-co-5%-HV) on non-hydrolyzed whey lactose plus addition of valeric acid as 3HV precursor (q(p): 12.5 mg x g(-1) x h(-1)). A detailed characterization of the isolated biopolyesters and an evaluation with regard to the economic feasibility completes the study. 相似文献
12.
Li Y Wu J Qi D Xu X Deng C Yang P Zhang X 《Chemical communications (Cambridge, England)》2008,(5):564-566
A novel approach is proposed to synthesize Fe(3)O(4)@TiO(2) microspheres with a well-defined core-shell structure, and the synthesized Fe(3)O(4)@TiO(2) core-shell microspheres were successfully applied for the simple and fast enrichment of phosphopeptides via direct MALDI-TOF mass spectrometry analysis. 相似文献
13.
A novel process is described to efficiently photoconvert low-grade organic materials such as waste biomass into natural biological
plastics. When heterogeneous forms of dry biomass are thermally gasified, relatively homogeneous synthesis gas mixtures composed
primarily of carbon monoxide and hydrogen are produced. Unique strains of photosynthetic bacteria were isolated that nearly
quantitatively photoassimilate the carbon monoxide and hydrogen components of synthesis gas into new cell mass. Under unbalanced
culture conditions when cellular growth is limited by shortages of nitrogen, calcium, magnesium, iron, or essential vitamins,
up to 28% of the new cell mass is found as granules of poly-3-hydroxyalkanoate (PHA), a highmolecular-weight thermoplastic
that can be solvent-extracted. The dominant monomeric unit of PHAs is 3-hydroxybutyrate (3HB), which is polymerized into the
homopolymeric poly-3-hydroxybutyrate (PHB). PHB is marketed as a biodegradable plastic with physical properties similar to
polystyrene. When a green alga was cocultured with the photosynthetic bacterium in light-dark (day-night) cycles, the bacteria
synthesized a polymer of poly-3-hydroxybutyrate-3-hydroxyvalerate (PHB-V) with a composition of 70% 3HB and 30% 3-hydroxyvalerate
(3HV) to an extent of 18% of the new cell mass. PHB-V is commercially marketed as Biopol and has physical properties similar
to polypropylene or polyethylene. Our results demonstrate that a strain of photosynthetic bacteria capable of photoassimilating
synthesis gas or producer gas is a potential candidate for large-scale production of biological polyesters. 相似文献
14.
15.
Assessment of PHB with varying hydroxyvalerate content for potential packaging applications 总被引:1,自引:0,他引:1
Poly-(hydroxybutyrate) (PHB) is biodegradable aliphatic polyester that is produced by a wide range of microorganisms. Basic PHB has relatively high glass transition and melting temperatures. To improve flexibility for potential packaging applications, PHB is synthesized with various co-polymers such as poly-(3-hydroxyvalerate) (HV) leading to a decrease of the glass transitions and melting temperatures. In addition, the HV broadens the processing window since there is improved melt stability at lower processing temperatures. In this study, PHB synthesized with different valerate contents (5%, 12%, and 20%) and varying in molecular weights were characterized. All PHBV materials displayed a glass transition between −10 and 20 °C. The two melting transitions found for Aldrich 5%, 12%, and Tianan 20%, resulted from crystals formed during cooling of the samples. The complex viscosity decreased with increasing temperature due to a decrease in molecular weights of the samples. These results suggest that processing the co-polymer below 160 °C would be beneficial with low screw speed. The mechanical results indicate all PHBV materials had high elastic modulus and flexural strength with low tensile strength and elongation at break. The WVTR results indicated the polymer to be very hydrophilic, resulting in higher water transmission rates. 相似文献
16.
Xu S Ma WF You LJ Li JM Guo J Hu JJ Wang CC 《Langmuir : the ACS journal of surfaces and colloids》2012,28(6):3271-3278
An effective method was developed for synthesizing magnetite/polymer colloidal composite microspheres with controllable variations in size and shape of the nanostructures and desirable interfacial chemical functionalities, using surfactant-free seeded emulsion polymerization with magnetite (Fe(3)O(4)) colloidal nanocrystal clusters (CNCs) as the seed, styrene (St) as the monomer, and potassium persulfate (KPS) as the initiator. The sub-micrometer-sized citrate-acid-stabilized Fe(3)O(4) CNCs were first obtained via ethylene glycol (EG)-mediated solvothermal synthesis, followed by 3-(trimethoxysilyl)propyl methacrylate (MPS) modification to immobilize the active vinyl groups onto the surfaces, and then the hydrophobic St monomers were polymerized at the interfaces to form the polymer shells by seeded emulsion radical polymerization. The morphology of the composite microspheres could be controlled from raspberry- and flower-like shapes, to eccentric structures by simply adjusting the feeding weight ratio of the seed to the monomer (Fe(3)O(4)/St) and varying the amount of cross-linker divinyl benzene (DVB). The morphological transition was rationalized by considering the viscosity of monomer-swollen polymer matrix and interfacial tension between the seeds and polymer matrix. Functional groups, such as carboxyl, hydroxyl, and epoxy, can be facilely introduced onto the composite microspheres through copolymerization of St with other functional monomers. The resultant microspheres displayed a high saturation magnetization (46 emu/g), well-defined core-shell nanostructures, and surface chemical functionalities, as well as a sustained colloidal stability, promising for further biomedical applications. 相似文献
17.
Polyhydroxyalkanoate (PHA) synthase from Pseudomonas sp 61-3 (PhaC1(Ps)) is able to synthesize P(3HB-co-3HA), consisting of a 3HB unit and medium-chain-length 3HA units of 6-12 carbon atoms. Expression vectors encoding 76 PhaC1(Ps) mutants with an amino acid replacement at position 130, 325, 477 or 481 were individually introduced into Ralstonia eutropha. The mutant enzyme genes were evaluated in terms of their abilities to synthesize P(3HB-co-3HA) using soybean oil as a carbon source. 20 mutants showed significantly high accumulation levels of PHA exceeding 30 wt.-% and as high as 57 wt.-%. It was found that hydrophobic amino acids at the positions are more likely to enhance accumulation of PHA in R. eutropha. 相似文献
18.
采用二次生长法(外延法)在ZSM-5(MFI型)晶体颗粒表面外延生长SAPO-34(CHA型)磷酸硅铝分子筛壳层,合成了MFI/CHA型核壳分子筛材料。并利用X射线衍射(XRD)、扫描电镜(SEM)、能量色散射线光谱(EDS)和傅里叶变换红外(FTIR)光谱对其进行了表征。结果表明,核相ZSM-5的预处理步骤对于成功合成此核壳型分子筛材料十分关键。通过研究晶化温度和晶化时间对MFI/CHA核壳型沸石分子筛合成的影响推测出MFI/CHA壳层生长的晶化机理,并考察在甲醇芳构化中的择形催化作用。 相似文献
19.
聚羧基脂肪酸酯细菌合成的生长环境依赖性 总被引:4,自引:0,他引:4
聚羟基脂肪酸酯(Polyhydroxyalkanoate,PHA)是一类由许多细菌合成的、结构多变的能量和碳源的储藏物质,为了得到能合成新型PHA的菌种,或得到能在便宜简单碳源上合成PHA的菌种,以我们实验室开发的傅立叶红外(FT-IR)细胞无损检测技术和常规气相色谱(GC)法对全国各地的采集的不同样品中分离的菌种进行了筛选,往往在不同的地理环境中,筛选出的菌株所合成的PHA的单体组成不同,有以含四个或五个碳原子的短链单体PHA(Short-chain-lengthPHA,sclPHA)为主,有的以含六个到十六个碳原子的中长链单体PHA(Medium-chain-lengthPHA,mcl PHA)为主,在我们以六种底物为碳源培养的371株形态不一的菌株中,有40%的菌可以合成PHA,而其中许多可以同时合成PH 相似文献
20.
聚羟基脂肪酸酯细菌合成的生长环境依赖性 总被引:3,自引:0,他引:3
聚羟基脂肪酸酯 (Polyhydroxyalkanoate,PHA)是一类由许多细菌合成的、结构多变的能量和碳源的储藏物质 .为了得到能合成新型PHA的菌种 ,或得到能在便宜简单碳源上合成PHA的菌种 ,以我们实验室开发的傅立叶红外 (FT IR)细胞无损检测技术和常规气相色谱 (GC)法对全国各地的采集的不同样品中分离的菌种进行了筛选 .往往在不同的地理环境中 ,筛选出的菌株所合成的PHA的单体组成不同 ,有的以含四个或五个碳原子的短链单体PHA(Short chain lengthPHA ,sclPHA)为主 ,有的以含六个到十六个碳原子的中长链单体PHA(Medium chain lengthPHA ,mclPHA)为主 .在我们以六种底物为碳源培养的 371株形态不一的菌株中 ,有 40 %的菌可以合成PHA ,而其中许多可以同时合成PHB与中长链PHA共混的聚合物 .本研究为进行PHA研究的高分子同行提供了寻找能合成PHA的微生物菌种的依据 相似文献