Laccase/caffeic acid-catalyzed crosslinking coupled with galactomannan alters the conformational structure of ovalbumin and alleviates Th2-mediated allergic asthma

Ovalbumin(OVA)is the major allergenic protein that can induce T helper 2(Th2)-allergic reactions,for which current treatment options are inadequate.In this study,we developed a polymerized hypoallergenic OVA product via laccase/caffeic acid(Lac/CA)-catalyzed crosslinking in conjunction with galactomannan(Man).The formation of high molecular weight crosslinked polymers and the Ig G-binding were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis(SDS-PAGE)and Western blotting.The study indicated that Lac/CA-catalyzed crosslinking plus Man conjugation substantially altered secondary and tertiary structures of OVA along with the variation in surface hydrophobicity.Gastrointestinal digestion stability assay indicated that crosslinked OVA exhibited less resistance in simulated gastric fluid(SGF)and simulated intestinal fluid(SIF).Mouse model study indicated that Lac-Man/OVA ameliorated eosinophilic airway inflammatory response and efficiently downregulated the expression of Th2-related cytokines(interleukin(IL)-4,IL-5,and IL-13),and upregulated IFN-γand IL-10 expression.Stimulation of bone marrow-derived dendritic cells with Lac-Man/OVA suppressed the expression of phenotypic maturation markers(CD80 and CD86)and MHC class II molecules,and suppressed the expression levels of proinflammatory cytokines.The knowledge obtained in the present study offers an effective way to acquire a hypoallergenic OVA product that can have a therapeutic effect in alleviating OVA-induced allergic asthma.

骨肿瘤患者丙泊酚麻醉术后血清IL-1、Lac的表达与肺部感染的关系

目的 探讨骨肿瘤患者丙泊酚麻醉术后血清白介素1(IL-1)、乳酸(Lac)的表达与肺部感染的关系。方法回顾性分析接受手术治疗并行丙泊酚麻醉的80例骨肿瘤患者的临床资料,根据术后肺部感染情况将患者分为感染组(26例)和未感染组(54例)。术后对2组患者血清IL-1、Lac表达水平进行检测,并分析IL-1、Lac表达水平与肺部感染的关系。结果 与未感染组比较,感染组血清IL-1、Lac表达水平明显更高(P<0.05)。与轻度、中度感染组比较,重度感染组血清IL-1、Lac表达水平明显更高;与轻度感染组比较,中度感染组血清IL-1、Lac表达水平明显更高(P<0.05)。血清IL-1、Lac表达水平与轻度、中度、重度肺部感染呈正相关性(P<0.05)。血清IL-1联合Lac检测的灵敏度、特异度明显高于血清IL-1与血清Lac单独检测(P<0.05)。结论 血清IL-1、Lac表达水平与骨肿瘤丙泊酚麻醉术后肺部感染的发生存在一定关联,可根据其表达水平变化情况判断患者的肺部感染严重程度。

基于LAC理论的城市自然公园游憩承载力研究与应用

研究以城市自然公园游憩资源过量使用问题与新发展理念下公园建设、管理、运营为出发点,选取福州市鹤林生态公园为样地,基于LAC理论九步骤,借助对描述性、评价性两个类型承载力影响因子的可度量的集合与标度来反应公园游憩承载力现状,提出包括客容量评估、游憩管理及景观优化等方面的公园承载力研究新思路,并总结出一套城市自然公园游憩使用管理框架,以期成为解决容量过载、环境破坏、游憩满意度低等问题的新视角。研究结果表明:(1)鹤林生态公园瞬时游憩承载力为6460人次,日游憩承载力为25850人次;(2)公园设施、景观、自然三类ROS分区的游憩承载力有效率为0.644、0.545、0.580,设施型空间整体处于弱载状态,景观型、自然型空间处于适载状态,鹤林生态公园整体承载量适中,可持续发展态势良好,尚有进一步游憩开发潜力。

DNA去甲基化酶对拟南芥Laccase家族基因甲基化及转录模式的影响

植物Laccase家族蛋白,是铜蓝氧化酶超家族的重要成员,具有包括抗病性在内的多种生物学功能。利用拟南芥野生型及ros1、rdd和dme突变体的全基因组甲基化测序(BS-SEQ)数据,分析了拟南芥Laccase蛋白家族基因(AtLACs)的DNA甲基化模式。结果表明:在野生型和不同DNA去甲基化酶突变体中,该家族少数成员在基因上游区和转录区存在较高水平的甲基化修饰现象。转录组测序(RNA-SEQ)数据分析结果显示,在野生型和不同突变体中,ALAC家族基因的转录水平普遍较低。而AT5G48100基因在拟南芥胚乳细胞中剧烈表达,DME突变后,其表达水平进一步剧烈增强。综合而言,在野生型和不同DNA去甲基化酶突变体中,ALAC基因家族大部分成员的DNA甲基化修饰与转录调控关联不强,但有些基因的DNA甲基化程度与转录水平之间有密切联系。

NT-proBNP、cTnI、Lac联合检测与脓毒症心力衰竭预测相关性分析

目的:探讨NT-proBNP、Lac、cTnI联合检测与脓毒症心力衰竭预测的相关性。方法:选取医院重症医学科收治的82例脓毒症心力衰竭患者,所有患者均进行NT-proBNP(N末端B型利钠肽原)、Lac(动脉血乳酸)、cTnI(肌钙蛋白I)检测,并应用ROC曲线下面积(AUC)以对NT-proBNP、cTnI、Lac在脓毒症心力衰竭患者诊断中的敏感性、特异性进行统计,以对NT-proBNP、cTnI、Lac评估患者预后的价值进行分析。结果:不同心功能分级脓毒症心力衰竭患者NT-proBNP、Lac、cTnI水平比较,差异均有统计学意义(P<0.05),患者的心功能越差,NT-proBNP、Lac、cTnI水平越高。单独采用NT-proBNP检测的敏感性为75.61%,单独采用Lac检测的敏感性为64.63%,单独采用cTnI检测的敏感性为73.17%,脓毒症心力衰竭采用NT-proBNP、Lac、cTnI联合检测的敏感性为90.24%,与单项检测相比明显更高(P<0.05)。结论:采用NT-proBNP、Lac、cTnI联合检测方式能够有效地诊断早期脓毒症心力衰竭,从而为脓毒症心力衰竭的预防和早期诊治提供重要依据。

脓毒症预后不良患者血清I-FABP、DAO、D-Lac水平变化及其危险因素探讨

目的 探讨脓毒症预后不良患者血清肠型脂肪酸结合蛋白(I-FABP)、二胺氧化酶(DAO)、D-乳酸(D-Lac)水平变化及其危险因素。方法 收集2017年7月至2020年3月秦皇岛市第一医院收治的454例脓毒症患者临床资料,根据患者预后情况将其分为预后良好组(273例)和预后不良组(181例),统计脓毒症患者预后不良发生现状及其单因素,采用多因素Logistic回归分析脓毒症患者预后不良的危险因素。结果 454例脓毒症患者预后不良共181例,预后不良发生率为39.87%。单因素分析结果显示,预后不良组与预后良好组年龄、平均动脉压(MAP)、急性生理与慢性健康状况评分Ⅱ(APACHEⅡ)评分、感染相关器官功能衰竭(SOFA)评分、外周血白细胞(WBC)、中性粒细胞(NEU)、血清C反应蛋白(CRP)、降钙素原(PCT)、尿素氮(BUN)、血肌酐(Scr)、总胆红素(TBil)、前白蛋白(PAB)、I-FABP、DAO、D-Lac、D-二聚体(D-d)水平及凝血酶原时间(PT)、活化部分凝血酶原时间(APTT)、国际标准化比值(INR)比较,差异具有统计学意义(P<0.05)。多因素Logistic回归分析结果显示,年龄较大、MAP较低、APACHEⅡ评分较高、SOFA评分较高、外周血NEU、血清CRP、PCT、BUN、Scr、DAO、D-Lac、D-d、I-FABP水平较高、PT、APTT较长均为脓毒症患者预后不良的独立危险因素(P<0.05)。结论 脓毒症患者预后不良发生率较高,同时其危险因素与患者年龄、MAP、APACHEⅡ、SOFA评分、外周血NEU、血清CRP、PCT、BUN、Scr、DAO、D-Lac、D-d、I-FABP水平、PT、APT有关。

Decolorization of reactive dyes by laccase immobilized in alginate/gelatin blent with PEG

To achieve effective decolorization of reactive dyes,laccase immobilization was investigated.Laccase 0.2%(m/V)(Denilite IIS) was trapped in beads of alginate/gelatin blent with polyethylene glycol(PEG),and then the supporters were activated by cross-linking with glutaraldehyde.The results of repeated batch decolorization showed that gelatin and appropriate concentration of glutaraldehyde accelerated the decolorization of Reactive Red B-3BF(RRB);PEG had a positive effect on enzyme stability and led to an inc...

Production of laccase by Coriolus versicolor and its application in decolorization of dyestuffs: (Ⅱ) Decolorization of dyes by laccase containing fermentation broth with or without self-immobilized mycelia

The capability of decolorization for commercial dyes by Coriolus versicolor fermentation broth containing laccase with or without immobilized mycelium was evaluated. With cell free fermentation broth containing laccase, high decolorization ratio was achieved for acid orange 7, but not for the other dyes concerned. The immobilized mycelium was proved to be more efficient than the cell free system. All the four dyestuffs studied were found being decolourized with certain extent by immobilized mycelium. The repeated batch decolorization was carried out with satisfactory results. The experimental data showed that the continuous decolorization of wastewater from a printing and dyeing industry was possible by using the self immobilized C. Versicolor.

Effects of nonionic surfactant Triton X-100 on the laccase-catalyzed conversion of bisphenol A

The laccase-catalyzed conversion of bisphenol A （BPA） in aqueous solutions was studied in the absence and presence of nonionic surfactant Triton X-100. It was found that the addition of Triton X-100 into the reaction system increased the conversion of BPA, especially near the critical micelle concentration of Triton X-100. Also it was found that the stability of laccase was greatly improved in the presence of TritonX-100. Studies on the endogenous fluorescence emission of laccase indicated that there existed an interaction between Triton X-100 and laccase, which was beneficial to folding and stabilizating of laccase. The binding of Triton X-100 to the laccase surface also mitigated the inactivation effect caused by the free radicals and polymerization products. Under otherwise identical conditions, a lower dosage of laccase was needed for the higher conversion of BPA in the presence of Triton X-100.

Decolorization on Indigo Dyeing Wastewater by Laccase from Coriolus versicolor

[ Object] The study aimed to discuss the decolorization on indigo dyeing wastewater by laccase from Coriolus versicolor. [ Method ] Firstly, the effects of temperature, pH, indigo concentration, HBT concentration, laccase dosage on the decolorization of indigo dyeing wastewater by laccase/HBT, and then the synergism of laccase and acid cellulase was analyzed. [Result] Using ABTS as the substrate, the kinetic parame- ters, K,, and Vmax, were 0.318 mmol/L and 0.035 5 mmol/（ L . min） respectively. The decolorization rate of indigo reached 96.5% when the lacca- se acted on indigo for 40 min with HBT as an introducer at temperature 50 ℃, pH =4.5, indigo concentration 100 mg/L, HBT concentration 0.1% and laccase dosage 100 lU/L. Due to the synergism of laccase and acid cellulase during the bio-finishing of blue jeans, the backstaining degree of blue jeans reduced by 85% when the amount of laccase added was 15 000 IU/kg. Menawhile, the synergism of the laccase and acid cellulase de- creased indigo concentration in wastewater by 83.8%. [ Conclusion ] The laccase from Coriolus versicolor had a good prospect in the bio-finishing of blue jeans and the decolorization of indigo dyeing wastewater.

Cloning,expression in Escherichia coli,and enzymatic properties of laccase from Aeromonas hydrophila WL-11

A strain WL-11 with high laccase activity was isolated from activated sludge collected from the effluent treatment plant of a textile and dyeing industry. It was identified as Aeromonas hydrophila by physiological test and 16S rDNA sequence analysis. A gene encoding of laccase from a newly isolated Aeromonas hydrophila WL-11 was cloned and characterized. Nucleotide sequence analysis showed an open reading frame of 1605 bp encoding a polypeptide comprised of 534 amino acids. The primary structure of the enzyme predicted the structural features characteristic of other laccases, including the conserved regions of four histidine-rich copper-binding sites. The predicted amino acid sequence showed a high homology （more than 60%） with bacterial laccases in the genome and protein databases and the highest degree of similarity （61% identity） was observed with the multicopper oxidase of KlebsieUa sp. 601. When expressed in Escherichia coli, the recombinant enzyme was overproduced in the cytoplasm as soluble and active form. The purified enzyme had an optimum pH of 2.6 and 8.0 for ABTS （2,2＇-azino-bis（3-ethylbenzthiazolinesulfonic acid） and DMP （2,6-dimethoxyphenol）, respectively. The kinetic study on ABTS revealed a higher affinity of this enzyme to this substrate than DMP.

Preparation of Magnetic Chitosan Nanoparticles and Immobilization of Laccase

The magnetic chitosan nanoparticles were prepared by reversed-phase suspension method using Span-80 as an emulsifier, glutaraldehyde as cross-linking reagent. And the nanoparticles were characterized by TEM, FT-IR and hysteresis loop. The results show that the nanoparticles are spherical and almost superparamagnetic. The laccase was immobilized on nanoparticles by adsorption and subsequently by cross-linking with glutaraldehyde. The immobilization conditions and charac-terizations of the immobilized laccase were investigated. The optimal immobilization conditions were as follows： 10 mL of phosphate buffer （0.1 M, pH 7.0） containing 50 mg of magnetic chitosan nanoparticles, 1.0 mg·mL-1 of laccase and 1% （v/v） glutaraldehyde, immobilization temperature of 4 ℃ and immobilization time of 4 h. The immobilized laccase exhibited an appreciable catalytic capability （480 units·g-1 support） and had good storage stability and operation stability. The Km of immobilized and free laccase for ABTS were 140.6 and 31.1 μM in phosphate buffer （0.1 M, pH 3.0） at 37 ℃, respectively. The immobilized laccase is a good candidate for the research and development of biosensors based on laccase catalysis.

Rhus laccase catalysis and product characterization of 1,2-dimethoxyphenol in organic solutions

Dimethoxyphenol was a widely used substrate in determination of laccases activity. It was surprised, however, that the products of it had not been completely determined until now. Studies were thus conducted on Rhus laccase （RL） and immobilized Rhus laccase （IRL）-catalyzed oxidation of 2,6-dimethoxyphenol （DMP） in water-organic solvent systems. Only one product, 3,3′,5,5′- tetramethoxy-1 ,1′-biphenyl-4,4′-diol （TMBP）, was produced by RL catalysis, and it was thoroughly characterized by FT-IR, NMR and GC-MS, etc.

Organic Solvents Enhanced Spectrofluorimetric Method for Determination of Laccase Activity

A novel fluorimetric method for determination of laccase activity in organic solvents is proposed, based on the oxidation ofo-phenylenediamine (1,2-diaminobenzene, OPDA) catalyzed by laccase yielding 2,3-diaminophenazine. The optimal conditions for laccase in organic media areT=55°C, pH=6.5, 1.0×10?2mol/L OPDA, 1.25 mL ethanol, 1.25 mL 1,4-dioxane and 1.25 mL acetone. The linear range of the method proposed in ethanol, 1,4-dioxane and acetone media were 0.44–19.33, 0.11–20.85, 0.38–21.05 U with the detection limit of 0.088, 0.022, 0.076 U, respectively. The proposed method has been applied to the analysis of laccase activity of real samples with more accurate and sensitive than that of the previous method reported.

Properties of crude laccase from Trametes versicolor produced by solid-substrate fermentation

A low-cost process for the production of laccases is necessary for a sustainable enzymatic wastewater treatment. Therefore, it is necessary to establish an easy and low-cost procedure for the production of laccase. In the present study the properties of crude laccase from Trametes versicolor produced by solid-substrate fermentation is investigated. The application of the enzyme for dye decolorization is also studied. Crude laccase from the studied culture established maximal activity at 45&#186;C. The enzyme retained over 90% of its activity in the temperature range 40- 47&#186;C and pH 4.5. The kinetic constants of the crude enzyme was also determined. In the presence of KCl, NaCl, CaCl2, MnSO4 and MgSO4, laccase demonstra- ted high stability—over 50% of its initial activity was still retained after 4-month incubation. Complete loss of enzymatic activity was observed in the presence of CuCl2, FeCl2, FeCl3 and NaN3 after 30 min of incubation. 100% decolorization by investigated crude laccase was completed in the case of Indigo Carmine for 4 h, Remazol Brilliant Blue R—for 6 h, Orange II— for 48 h and Congo Red—for 13 d.

Production of laccase by Coriolus versicolor and its application in decolorization of dyestuffs: (Ⅰ) Production of laccase by batch and repeated-batch processes

The production of laccase by Coriolus versicolor was studied. The effect of cultivation conditions on laccase production by Coriolus versicolor was examined to obtain optimal medium and cultivation conditions. Both batch and repeated batch processes were performed for laccase production. In repeated batch fermentation with self immobilized mycelia, total of 14 cycles were performed with laccase activity in the range between 3.4 and 14.8 U/ml.

Cloning of multicopper oxidase gene from <i>Ochrobactrum sp</i>. 531 and characterization of its alkaline laccase activity towards phenolic substrates

A 1602 bp fragment was cloned from a soil bacterium Ochrobactrum sp. 531. It contained an open reading frame (ORF) of 1092 bp which was identified as a multicopper oxidase (MCO) with potential laccase activity. After inserting the cloned gene into the expression vector pET23a, it was expressed in E. coli BL21(DE3)pLysS, and its product was purified to homogeneity through chromatography. The Ochrobactrum sp. 531 MCO, consisting of 533 amino acids with a molecular mass of 57.8 kDa, was quite stable in neutral pH and showed laccase-like activity oxidizing 2,6-dimethoxyphenol (DMP), 2,2’-azino-bis(3-ethylbe- nzthiazolinesulfonic acid) (ABTS), and syringaldazine (SGZ). The enzyme showed optimum activity towards DMP, ABTS, and SGZ at the pH 8.0, 3.6, and 7.5 respectively. Kinetic studies gave this enzyme Km, kcat and kcat//Km values of: 0.09 mM, 7.94 s–1, and 88.22 s–1?mM–1 for DMP;0.072 mM, 2.95 s–1, and 40.97 s–1.mM–1 for ABTS;and 0.015 mM, 2.4 s–1, and 160 s–1.mM–1 for SGZ. Our results demonstrate that Ochrobactrum sp. 531 MCO is a bacterial laccase which oxidized phenolic substrates DMP and SGZ effectively under alkaline conditions. These unusual properties make the enzyme an interesting biocatalyst in applications for which classical laccases are unsuitable.

Effects of laccase incubated from white rot fungi on the mechanical properties of fiberboard

White rot fungi were optimized to cultivate highly active laccase. The characteristics of laccase incubated by continuous culture were compared with those of direct culture. The enzyme activity of laccase incubated by continuous culture technology reached a higher value on the fifth day of the growth. The optimization incubation time of high activity laccase was the eleventh day. A large amount of highly active laccase can be obtained in a relatively short time by continuous culture to replace traditional laccase. After laccase treatment, the lignin composition of wood fibers were oxidation-catalyzed by laccase. The number of chemical-bonding points between the wood fibers was increased. The wood fibers treated by laccase were fabricated into boards and their mechanical properties improved with the laccase-incubation times. Compared with the fiberboards made from fibers that were pre-treated by laccase of incubation 5 days, the static bending strength of those that were pre-treated by laccase of incubation 11 days was increased by 18.95%, the elastic modulus was increased by 35.49%, and the internal bond strength was increased by 44.11%.

Molecular identification and enzymatic properties of laccase2 from the diamondback moth Plutella xylostella (Lepidoptera:Plutellidae)

Laccase（EC 1.10.3.2）is known to oxidize various aromatic and nonaromatic compounds via a radical-catalyzed reaction,which generally includes two types of laccase,Lac1 and Lac2.Lac1 oxidizes toxic compounds in the diet,and Lac2 is known to play an important role in melanizing the insect exoskeleton.In this study,we cloned and sequenced the cDNA of the diamondback moth,Plutella xylostella Lac2（PxLac2）,from the third instar larvae using polymerase chain reaction（PCR）and rapid amplification of cDNA ends techniques.The results showed that the full-length PxLac2 cDNA was 1 944 bp long and had an open reading frame of 1 794 bp.PxLac2 encoded a protein with 597 amino acids and had a molecular weight of 66.09 kDa.Moreover,we determined the expression levels of PxLac2 in different stages by quantitative PCR（qPCR）.The results indicated that PxLac2 was expressed differently in different stages.We observed the highest expression level in pupae and the lowest expression level in fourth instar larvae.We also investigated the enzymatic properties of laccase,which had optimal activity at pH 3.0 and at 35°C.Under these optimal conditions,laccase had a Michaelis constant（Km）of 0.97 mmol L-1,maximal reaction speed（Vm）of 56.82 U mL-1,and activation energy（Ea）of 17.36 kJ mol-1 to oxidize2,2＇-azino-bis（3-ethylbenzothiazoline-6-sulfonic acid ammonium salt）.Type II copper enhanced laccase activity below 0.8mmol L-1 and reduced enzyme activity above 0.8 mmol L-1 with an IC50 concentration of 1.26 mmol L-1.This study provides insights into the biological function of laccase.

Isolation,expression and single nucleotide polymorphisms(SNPs) analysis of LACCASE gene(LkLAC8) from Japanese larch(Larix kaempferi)

Nucleotide diversity (pi) and linkage disequilibrium (LD) analysis based on SNP marker could provide a sound basis for choosing an association analysis method. Japanese larch (Larix kaempferi) is an important timber coniferous tree species for pulping and papermaking, but its high lignin content has significantly restricted it application potential. In this study, the LACCASE gene, that plays an important regulatory role for lignin biosynthesis, was selected as research target. The full-length cDNA and genomic sequences of the encoding LkLAC8 gene were isolated from the LACCASE expressed sequence tags of the Japanese larch transcriptome database using the rapid amplification of cDNA ends-polymerase chain reaction (RACE-PCR). The cDNA was determined to be 1940 bp, with an open reading frame (ORF, 1734 bp) that encoded a protein of 577 AA. This protein contains four highly specific Cu2+ binding sites and 11 glycosylation sites, thus belonging to the LACCASE family. The deduced protein sequence shared an 89% identity with the PtaLAC from Pinus taeda. A real-time PCR analysis showed that the LkLAC8 transcript was expressed predominantly in mature xylem, with moderate levels in the immature xylem, cambium and mature leaves, the lowest in the roots. Lastly, the genomic sequences of LkLAC8 in 40 individuals from six naturally distributed populations of Japanese larch were amplified, and a total of 201 SNPs (103 and 98 mutation types of transition and transversion, respectively) were detected; the frequency of the SNPs was 1/19 bp. Nucleotide diversity among the six populations ranged from 0.0034 to 0.0053, which suggested that there were no significant differences among the populations. The LD analysis showed that the LD level decayed rapidly within the increasing length of the LkLAC8 gene. These results implied that LD mapping and association analysis based on candidate gene may be feasible for the marker-assisted breeding of new germplasms with low lignin in Japanese larch.