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1.
A total of 117 agar-decomposing cultures were isolated from coastal seawater around Qingdao,China.The phenotypic and agarolytic features of an agarolytic isolate,QM38,were investigated.The strain was gram negative,strictly aerobic,curved rod and polar flagellum.On the basis of several phenotypic characters,biochemical and morphological characters and phylogenetic analysis of the gene coding for the 16S rRNA,the strain was identified as Agarivorans albus strain QM38.This strain can liquefy the agar on the solid agar plate.An excellular agarase activity was determined in liquid culture.The enzyme exhibited maximal activity at 40℃,pH 7.6.Its activity was greatly affected by different concentrations of agarose.The highest activity 32 U/ml was achieved in the culture supernatant.The hydrolytic product was analyzed by fluorophore-assisted carbohydrate electrophoresis (FACE).After complete hydrolysis of agarose,a series of agaro-oligosaccharides were produced.The main products of the enzymes were oligosaccharides in the degree of polymerization (DP) of 2,4,6 and 8.Three genes agaD01,agaD02 and agaD03,encoding β-agarases,had been cloned from genomic DNA of Agarivorans albus strain QM38.The open reading frame of agaD01,consisted of 2 988 bp,and shared 95.5%-98.9% identity to the β-agarase genes of some strains of Vibrio and Agarivorans.Gene agaD02 comprised 2 868 bp and encoded a 955-amino-acid protein.It showed 97.4% and 98.7% identity to the β-agarase genes of strain Vibrio sp.PO-303 and strain Vibrio sp.JT0107,respectively.Only partial sequence of agaD03 gene has been cloned.It showed 96.5% identity to β-agarase gene (agaB) of Pseudoalteromonas sp.CY24,and shared 96.8% identity to β-agarase-c gene of Vibrio sp.PO-303. 相似文献
2.
Bacillus sp. JM7, a strain isolated from the deep-sea of the South China Sea, was found to efficiently degrade 79.4% native chicken feather within 30 h. Scanning electron microscopy analysis showed that JM7 strain could gradually degrade feather by modifying the microstructure of feather keratin. A total of 25 protease genes were predicted from the draft genome of JM7 strain, among which a predicted subtilisin-like serine protease(designated as Ker02562) was further characterized for its keratinolytic activity. The recombinant Ker02562 functioned at a wide range of temperatures from 30℃ to 60℃, with an optimum at 40–50℃. Ker02562 was highly active at various pHs ranging from 5.0 to 13.0, with a maximum activity observed at pH 7.0–9.0. Remarkably, recombinant Ker02562 was stable in extreme alkaline environments(pH 10–13), which was much better than most other reported keratinases. Collectively, these favorable properties could make Bacillus sp. JM7 and Ker02562 attractive to be applied in the detergent formulation and feather bioconversion. 相似文献
3.
ZHU Yanbing LIU Guangming LI Hebin LIU Jingwen BAI Xiaoming GUAN Rong CAI Huinong 《海洋学报(英文版)》2012,31(6):117-126
The gene(741 bp) encoding carboxylesterase from the thermophilic bacterium Geobacillus sp.ZHl was cloned and overexpressed in Escherichia coli.The purified recombinant protein presented a molecular mass of about 40 kDa by SDS-PAGE analysis.Enzyme assays using p-nitrophenyl esters with different acyl chain lengths as the substrates confirmed its esterase activity,yielding highest specific activity with p-nitrophenyl acetate.Among the p-nitrophenyl esters tested,the carboxylesterase presented preference for p-nitrophenyl caprylate,but hydrolyzed p-nitrophenyl butyrate more efficiently.When p-nitrophenyl butyrate was used as a substrate,the recombinant carboxylesterase exhibited highest activity at pH 8.0 and 60℃.Almost no decrease in esterase activity was observed at 60℃for 3 h,and over 40% of activity was still maintained after incubation at 90℃for 3 h.These results indicate that Geobacillus sp.ZH1 recombinant esterase was thermostable.The enzymatic activity was inhibited by the addition of phenylmethylsulfonyl fluoride,indicating that it contains serine residue,which plays a key role in the catalytic mechanism.Except SDS and xylene,this esterase showed stability toward other tested detergents and organic solvents.Cloning,expression,and biochemical characterization of Geobacillus sp.ZH1 carboxylesterase lay a good foundation for its structural characterization and industrial application. 相似文献
4.
Lectins are sugar-specific binding proteins or glycoproteins that play important physiological roles in cellular recognition and regulation. And they are also valuable in medicine and pharmacy. Tubeworm is the representative species around the hydrothermal vent in the deep sea. They have developed unique mechanisms to adapt to the harsh environment. In this study, a 1 092 bp c DNA, designed as rpgal, was first cloned and characterized from the tubeworm Ridgeia piscesae. Sequence analysis showed that RPGAL had low homology with the known galectin. And it had two homologous carbohydrate-recognition domains, which is the characteristic of the tandem-repeat type galectins. The RPGAL was successfully recombinant expressed in Escherichia coli and purified. Analysis of biological activity revealed that RPGAL was metal ion independent and it could agglutinate all the vertebrate erythrocytes tested. It was stable at 10–50°C and p H 5–10. And the hemagglutinating activity of RPGAL was strongly inhibited by D-Lactose and lipopolysaccharide. Although RPGAL had no effect on the microorganisms tested, it showed anti-tumor activity towards He La cells and HT1080 cells, which was accomplished by apoptosis. The study demonstrated that RPGAL was a novel galectin and provided a potential candidate for therapy of anti-tumor. 相似文献
5.
Effect of salinity on the growth, biological activity and secondary metabolites of some marine fungi
HUANG Jingjing LU Chunhu QIAN Xiaoming HUANG Yaojian ZHENG Zhonghui SHEN Yuemao 《海洋学报(英文版)》2011,30(3):118-123
The study investigated the effects of salinity on growth,antimicrobial activities and secondary metabolites of 47 marine filamentous fungi isolated from the East China Sea near the western shore of the Taiwan Straits.The results indicate that NaCl promoted the growth up to 91.5% of test strains.However,only 14.9% of them showed a significant increase of antimicrobial activity against Candida albicans.When incubated in different concentrations of NaCl,the colony growth, antimicrobial activities and composition of secondary metabolites of the strain Ty01b-8 of Penicillium sp.varied.Treatment with KCl also showed a similar effect.An alkaloid isolated from the fermentation broth of Ty01b-8 was identified as chrysogine,inhibition activity of which against Hela cells was 15.05% at 20 μ g/ml,and yield was 4.4 and 4.9 times higher in 3 percent and 6 percent NaCl treatments,respectively, compared with the non-salt culture condition. These findings prove that salinity is an important factor influencing growth and secondary metabolites of some marine fungi,which can be used to screen for new metabolites from marine fungi,and to enhance their metabolites production in industrial fermentation. 相似文献
6.
Thermostable SOD is a promising enzyme in biotechnological applications. In the present study, thermophile Geobacillus sp. EPT3 was isolated from a deep-sea hydrothermal field in the East Pacific. A thermostable superoxide dismutase(SOD) from this strain was purified to homogeneity by steps of fractional ammonium sulfate precipitation, DEAE-Sepharose chromatography, and Phenyl-Sepharose chromatography. SOD was purified 13.4 fold to homogeneity with a specific activity of 3 354 U/mg and 11.1% recovery. SOD from Geobacillus sp. EPT3 was of the Mn-SOD type, judged by the insensitivity of the enzyme to both KCN and H2O2. SOD was determined to be a homodimer with monomeric molecular mass of 26.0 k Da. It had high thermostability at 50°C and 60°C. At tested conditions, SOD was relatively stable in the presence of some inhibitors and denaturants, such as β-mercaptoethanol(β-ME), dithiothreitol(DTT), phenylmethylsulfonyl fluoride(PMSF), urea, and guanidine hydrochloride. Geobacillus sp. EPT3 SOD showed striking stability across a wide p H range from 5.0 to 11.0. It could withstand denaturants of extremely acidic and alkaline conditions, which makes it useful in the industrial applications. 相似文献
7.
Immediately following a spill at sea, released oil—ranging from diesel to light crude and diluted bitumen, will initially weather through evaporation, resulting in an elevated concentration of light hydrocarbons in the air. As part of oil spill response operations, first responders use hand-held devices to monitor airborne concentrations when approaching a spill. The feasibility of using numerical modelling as an additional tool to assess potential flammability and plan response operations in the spill area was explored in this study. The Lower Explosive Limit(LEL) is defined as the minimum concentration of a gas in air, in this case a mixture of evaporated hydrocarbons, which can produce a flash fire in the presence of an ignition source. This ignition source could be triggered by the vessel itself or by spill response operations. A framework was put into place, utilizing a threedimensional hydrodynamic model(H3D), an oil spill model(SPILLCALC), and an air dispersion model(CALPUFF) to assess the risk of possible ignition of the hydrocarbon vapour in the event of a spill. The study looked at a hypothetical credible worst case tanker spill(16 500 m~3) of diluted bitumen(cold lake winter blend)occurring at Arachne Reef in Haro Strait, British Columbia, Canada. SPILLCALC provided one-minute averaged vapour fluxes from the water surface for each of 17 modelled pseudo-components which were used as inputs to CALPUFF. Using the predicted airborne concentrations of each pseudo-component, time-scaled to one-second averages, the flammability potential in the immediate spill area was determined at each grid point using Le Chatelier's mixing equation. The approach describe here was developed as a proof of concept, and could be established as a real-time system, bringing valuable information in addition to hand-held devices during a spill response, or during a response exercise. This modelling study was conducted as part of Kinder Morgan's Trans Mountain Pipeline Expansion Project. There are a number of commercially available oil spill models but few if any are equipped with the ability to model air dispersion and forecast hazardous conditions as discussed in this paper. 相似文献
8.
CHEN Guohu HUANG Liangmin TAN Yehui YIN Jianqiang WANG Hankui HUANG Hui ZOU Kun LI Ruiping 《海洋学报(英文版)》2007,26(2):140-143
Coral mucus covers the surface of coral and contains antibacterial substances as a first line of defense. Coral mucus not only enables the coral itself to resist disease, but also provides antibacterial agents for people. We collected mucus from a scleractinian coral (Symphyllia gigantea) at Sta. Sanya (China), then extracted the antibacterial substances using 10% glacial acetic acid with the help of antiprotease inhibitors, and tested the antibacterial activity by a terrestrial bacterium (Staphylococcus aureus) and a marine bacterium (Vibrio anguillarum). The result showed that, there were antibacterial agents in the mucus, and their antibacterial activities were lost by treatment of the sample at 90 ℃ water for 10 min. 相似文献
9.
ZHU Yanbing LI Hebin ZHANG Xuqin ZHANG Chunyan XIANG Jionghu LIU Guangming 《海洋学报(英文版)》2011,30(6):95-103
A thermostable superoxide dismutase (SOD) from the inshore thermophile Thermus sp. JM1 was purified to homogeneity by steps of fractional ammonium sulfate precipitation, DEAE-Sepharose chromatography and Phenyl-Sepharose chromatography. The specific activity of the purified native enzyme was 1 656 U/mg. A sod gene from this strain was cloned and overexpressed in Escherichia coli (E. coli). The prepared apo-enzyme of the purified recombinant SOD (rSOD) was reconstituted with either Fe or Mn by means of incubation with appropriate metal salts. As a result, only Mn 2+ - reconstituted rSOD (Mn-rSOD) exhibited the specific activity of 1 598 U/mg. SOD from Thermus sp. JM1 was Mn-SOD, judging by the specific activities analysis of Fe or Mn reconstituted rSODs and the insensitivity of the native SOD to both cyanide and H 2 O 2 . Both the native SOD and Mn- rSOD were determined to be homotetramers with monomeric molecular mass of 26 kDa and 27.5 kDa, respectively. They had high thermostability at 50 ° C and 60 ° C, and showed striking stability across a wide pH span from 4.0 to 11.0. 相似文献
10.
Under artificial LD cycles(6,12,18 L),the elvers of Japanese eel,Anguilla japonica,showed a 24 h cycle of locomotor activity rhythm being most active at light transitions:the eels' activity rose to a primary peak after lights-off,followed by a quiescent period during which they buried into the shelters or lying motionlessly on sand for most of the time,and then reached a secondary peak before lights-on.Elvers could resynchronize their activity rhythm with a new photo cycle within 4 d.Moreover,their activity level at dark phase significantly increased as the light period was prolonged:higher activity levels during shorter dark period.However,the elvers did not display clearly the existence of a circadian rhythm under constant light or dark conditions.The timing of daily activity rhythm evidenced in the Japanese eels may occur through the action of the LD cycles with a weak participation of an endogenous circadian system.In all the LD cycles,over 99% of the activity occurred in the dark phase,indicating that the eels were always nocturnally active no matter what time of day it might be.Under 12 L conditions,the eels' activity level and the time outside sand were significantly elevated both at light and dark phases as temperature increased from 10~15 to 20~25 ℃.The activity rhythm pattern(i.e.,two peaks occurring around light transitions) did not apparently change among temperatures.However,in contrast with the primary activity peaks immediately after lights-off at 20 and 25 ℃,the timing of the primary peaks at 10 and 15 ℃ showed a latency of a few hours following lights-off,indicating the inhibiting effect of low temperature on the eels' activity. 相似文献
11.
褐球固氮菌(Azotobacter chroococcum)是一种海藻酸降解菌.本实验采用PCR的方法,以褐球固氮菌基因组DNA为模板,克隆出约1.05 kb的海藻酸裂解酶基因algL的成熟蛋白编码序列,并将其插入巴斯德毕赤酵母(Pichia pastoris)表达载体pPIC9K中,获得重组质粒pPIC9K-algL.重组质粒线性化后用聚乙二醇(PEG)法导入毕赤酵母菌株GS115中,获得高效分泌表达海藻酸裂解酶的毕赤酵母工程菌株.用甲醇诱导培养基进行摇瓶发酵,表达得到43 kDa的目的蛋白,酶活力可达1 400 U/cm3左右.经测定,该重组酶的最适反应pH为8.5,最适反应温度为40℃,并且在20~55℃,pH2.0~11.0具有较好的稳定性.另外,10 mmol/cm3的Cu2+,Fe2+,Co2+,Mn2+和Ca2+对酶有不同程度的抑制作用. 相似文献
12.
一株产褐藻酸多糖的海洋假单胞细菌Pseudomonas sp.QDA的筛选和鉴定 总被引：9，自引：0，他引：9
根据已获褐藻酸多糖生物合成基因簇中褐藻胶裂解酶基因(αlgL)的序列设计特异性引物，利用PCR技术从海洋微生物中筛选到1株能够分泌胞外多糖的细菌。采用形态学观察和16S rDNA序列分析鉴定该菌株，结果为假单胞属细菌，命名为Pseudomonas sp.QDA；系统发育树显示该菌株与P.putida亲缘关系最近。菌株产生的胞外多糖可被褐藻胶裂解酶(AlgL)降解，并在紫外234nm处检测到特征性吸收，初步证明含有褐藻酸多糖。 相似文献
13.
为获得古罗糖醛酸(Guluronate)含量高的细菌胞外褐藻多糖,利用PCR从海洋细菌Pseudomonassp.QDA中克隆了其甘露糖醛酸C-5差向异构酶基因(algG),连接入质粒pMF 54Km,构建了重组表达载体pMF54 Km-algG。利用三亲接合法将pMF54 Km-algG转入菌株QDA中,获得algG过量表达重组菌株QDA-G1。H-NMR测定结果表明,QDA-G所产的褐藻多糖中β-D-甘露糖醛酸(M)与它的C-5差向异构体α-L-古罗糖醛酸(G)的比值为0.38,G的质量分数达到74.2%,比野生菌株QDA提高了26.4%。且重组菌株遗传稳定性良好,连续传代20代后,M/G的比值无明显变化。 相似文献
14.
15.
Pseudomonas sp．QDA是从海水中发现的产生褐藻多糖的细菌，无致病性。为提高QDA菌株褐藻多糖的产量。本文利用PCR克隆了粘性菌株P．aeguginosa FRD1的atgT基因，连接入质粒pMF36-Kan，构建了重组表达载体pMF36-Kan-algT。利用三亲接合法将pMF36-Kan-algT转入菌株QDA中。糖醛酸含量测定结果表明，atgT基因过量表达菌株的褐藻多糖产量比出发菌株QDA平均提高了3．3倍，其中菌株A25提高了4．5倍。通过培养条件的进一步优化，A25菌株的褐藻多糖产量与菌株QDA相比提高到8．18倍。 相似文献
16.
褐藻低聚糖对提高大菱鲆免疫机能的作用 总被引：6，自引：0，他引：6
研究了在养殖过程中投喂酶解制备的褐藻低聚糖对大菱鲆(Scophthalmus maximus)鱼苗免疫机能的影响,对大菱鲆鱼苗血液中的酸性磷酸酶、过氧化物酶、超氧化物歧化酶和头肾淋巴细胞吞噬能力进行了测定。实验发现,褐藻低聚糖能够提高大菱鲆血液中酸性磷酸酶、过氧化物酶、超氧化物歧化酶活力;头肾淋巴细胞吞噬率较对照组提高15.4%,吞噬指数则无显著差异。结果表明在大菱鲆鱼苗的养殖过程中褐藻低聚糖可作为一种非特异免疫调节剂提高大菱鲆机体的免疫能力。 相似文献
17.
海洋脂肪酶ADM47601固定化方法的研究 总被引：1，自引：1，他引：0
采用海藻酸钠、壳聚糖、聚乙烯醇和明胶等材料, 进行对脂肪酶ADM47601的固定化研究。结果表明, 使用壳聚糖固定化脂肪酶, 在最优条件为2% (W/V)壳聚糖, 10% NaOH, 1%乙酸, 0.25%戊二醛, 每克载体添加840U脂肪酶时, 最大固定化酶活力回收率为87.06%。使用海藻酸钠-明胶固定化脂肪, 在最优固定化条件下, 最大固定化酶活力回收率为54.45%。使用聚乙烯醇固定化脂肪酶, 在最优固定化条件下, 最大固定化酶活力回收率为33.22%。使用海藻酸钠固定化脂肪酶, 在最优固定化条件下, 最大固定化酶活力回收率为17.11%。对比四种不同固定化酶方法, 脂肪酶活力回收率高度高低顺序为: 壳聚糖吸附交联法>海藻酸钠明胶协同包埋法>聚乙烯醇-硼酸法>海藻酸钠包埋法。 相似文献
18.
褐藻寡糖具有多种生理活性,本研究通过酶解与分级条件的优化,获得了低分子质量褐藻寡糖的酶法制备工艺,并在体外模型上评价了不同分子质量组分的抗氧化活性。结果表明,优化后的褐藻寡糖制备条件为:底物浓度1.20%,酶底比4.35 U/mg,酶解时间4 h。进一步采用乙醇沉淀和超滤分离后,获得了重均分子质量分别为0.84、1.40、2.25和34.56 k Da的4种组分,其得率分别为50.82%、5.15%、11.48%和12.00%。各组分均具有一定的还原能力,可有效清除DPPH和羟自由基,其中低分子质量组分A的抗氧化活性最为显著,其清除羟自由基的能力与维生素C相近。 相似文献