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1.
从北极王湾地区湖泊沉积物中分离出的菌株AFN2001,其代谢产物对金黄色葡萄球菌有明显的抑制作用,抑菌圈直径达23 mm,对大肠杆菌和绿脓杆菌没有抑制作用。为了确定AFN2001菌株发酵获得最多的活性物质,对单因素确定的营养因素淀粉、黄豆浸出物、蔗糖和NaNO3及另外的MgSO4、K2HPO3和水质进行7因素3水平正交优化实验。对结果进行直观分析及方差分析,发现NaNO3对发酵液活性的影响最大,其次依次为淀粉、K2HPO3、MgSO4、黄豆浸出物、蔗糖和水质对发酵液活性的影响;并找出产生活性物质的最佳组合。确定优化培养基(淀粉为10 g、蔗糖为10 g、黄豆浸出物为6 g、MgSO4为0.5 g和自来水为1 000 mL)和优化发酵条件(发酵温度为28℃、起始pH值为6.0和装液量为50%)。利用优化培养基和优化发酵条件发酵的菌株AFN2001,其发酵液的抑菌活性是基础培养基发酵液的1.6倍。 相似文献
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红树林沉积物来源链霉菌HA6菌株发酵条件的优化 总被引：1，自引：0，他引：1
HA6菌株是分离自红树林沉积物中具有强抗菌活性的链霉菌．为提高其抗菌活性物质的产量,通过单因子试验及正交试验法对其包括发酵培养基的组成、接种量、通气量和发酵时间等发酵条件进行优化．研究表明其最佳摇瓶发酵培养基配方为：麦芽提取物质量为2．00g、可溶性淀粉质量为3．00g、豆饼粉质量为2．00g、（NH4）：SO。质量为1．00g、NaCl质量为3．00g、CaC03质量为0．50g、蒸馏水体积为100cm^3;最优发酵条件为：500em。摇瓶装液体积为150em。,接种量为8％,培养温度为28℃,初始pH为7．5,转速为200r／rain,培养时间为5d． 相似文献
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为了从海绵共附生微生物中寻找天然高效抗污损活性物质,本文针对前期研究获取的4株具有显著抗硅藻附着的活性菌株进行活性验证和比较,选出其中最优菌株进行菌种鉴定及发酵条件优化.比较了活性菌株对小新月菱形藻(Nitzschia closterium)、咖啡双眉藻(Amphora coffeaeformis)、碎片菱形藻(Nitzschia frustulum)附着的抑制活性,确定菌株UST050418-715为最优菌株;通过16S r DNA的测序分析,结合平板的菌落形态和扫描电镜下菌体特征,鉴定活性菌株UST050418-715为短小芽孢杆菌(Bacillus pumilus).为优化该菌株的培养条件,选择了酵母粉、蛋白胨、Na Cl、p H值进行四因素三水平的正交实验,对菌株培养条件进行优化.发现选择的4个因素对应的菌株发酵产物对硅藻附着的抑制活性大小不同,影响显著性顺序是酵母粉蛋白胨Na Clp H值,综合菌株发酵产物活性、粗提物产量和菌株生长情况进行分析,确定菌株UST050418-715基于海洋2216E培养基的最佳发酵条件为:蛋白胨含量7.5 g/dm3,酵母粉含量3 g/dm3,Na Cl含量10.45 g/dm3,p H值9.5. 相似文献
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对重组别藻蓝蛋白类荧光蛋白基因工程菌在装有150 mL液体培养基的250 mL摇瓶中的发酵条件进行优化.对起始pH值、接种量、诱导起始时间、诱导温度和时长以及IPTG浓度对重组荧光蛋白表达量进行了分析.结果表明,在装有150 mL液体培养基的250 mL摇瓶中,在起始pH值为7.5,6%接种量,培养温度为37℃,培养时长为3～5 h,诱导温度为22℃,IPTG浓度为0.2 mmol/L,诱导时长为7～8 h的条件下发酵重组别藻蓝蛋白类荧光蛋白,其表达量最高. 相似文献
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研究了不同因素对侧孢短芽孢杆菌（Brevibaci Uuslaterosporus）无菌滤液溶藻效果的影响,并对无菌滤液进行了紫外光谱扫描分析,探讨侧孢短芽孢杆菌溶藻活性代谢产物的物质特性、探究物质的组成成分．结果显示：无菌滤液分别经不同温度、pH值、蛋白酶和紫外照射时间处理后,均仍具有极为显著的溶藻能力（P〈0．01）,溶藻实验7d后颤藻（Oscillatoria sp．）叶绿素a质量浓度的平均下降率分别为：58．65％、63．88％、61．50％和62．61％,藻体干重的平均下降率分别为：39．77％、39．30％、36．49％和37．02％,表明溶藻活性代谢物质具有耐酸、耐碱、耐高温、抗蛋白酶水解、抗紫外辐射的特性;同时,分别在4、28℃环境中贮存28d的无菌滤液,始终保持着极高的溶藻活性,溶藻实验7d后颤藻叶绿素a质量浓度的平均下降率分别为：50．84％和60．39％,藻体干重的平均下降率分别为：37．82％和37．54％,说明该物质的结构极其稳定,在环境中可长久存在;另外,加热与未加热处理的无菌滤液的紫外光谱最大吸收峰都在290～300nm之间．分析表明,溶藻活性代谢产物极大程度上属于具有极强稳定性的肽类物质． 相似文献
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从油田污水中筛选得到一株产表面活性剂的细菌Lz-2,对其生理生化性能及产物特性进行了测定,并初步分析了其产物结构。结果表明,该菌株为芽孢杆菌,在最佳培养条件即:柠檬酸钠为30g·L-1,蛋白胨为5g·L-1,氯化钠为5g·L-1,pH=9,温度为37℃时,发酵液的表面张力从最初75 mN·m-1降低到30.6mN·m-1,表面活性剂产量可达到1.228g·L-1,且该表面活性剂对多环芳烃具有良好的增溶性能,能使芘的表观溶解度增加1.25倍。 相似文献
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环状芽胞杆菌(Bacillus circulans)菌株FA13在M2培养基中的发酵无细胞上清液对寄生曲霉(Aspergillus parasiticus)突变菌株NFRI-95菌丝生长和黄曲霉毒素的产生表现出明显的抑制作用。为了最大限度地提高活性物质的产量,本研究对从南大西洋深海沉积物中分离到的环状芽胞杆菌菌株FA13的发酵条件进行了均匀设计发酵优化。优化后,菌株FA13的发酵液10倍稀释液对寄生曲霉突变菌株NFRI-95的菌丝生长抑制率从10.98%提高到70.57%,黄曲霉毒素产生抑制率从41.43%提高到100.00%;对应的发酵条件为发酵温度38.70 ℃,接种量6.00%,海水体积占比0.00%,培养基pH 8.71,培养时间6 d。 相似文献
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经紫外诱变,筛选出在碳酸氢铵浓度为400 mg/L条件下可以生存的突变株。通过培养基中氮、磷、铁、温度、光照及pH值对雨生红球藻诱变株生长的影响进行比较,对以上3种营养盐及3种环境因子分别进行三因素三水平正交实验,以优化培养条件。进而对雨生红球藻野生型及诱变株的生长状况及色素含量进行比较。实验结果表明,雨生红球藻抗铵品系在培养基中NaNO30.1 g/L,KH2PO40.01 g/L,FeCl3.6H2O 1.0 mg/L,在pH值为8.0,光照强度100μmol.m-2.s-1,温度为18℃的培养条件下,雨生红球藻的生物量得到有效提高。 相似文献
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一株溶藻细菌（Pseudoalteromonas sp．）的分离鉴定及溶藻活性初探 总被引：1，自引：0，他引：1
从海南洋浦港沉积物中分离到一株具有较强溶藻活性的细菌(编号Z3).通过对该菌株进行形态和生理测试以及16SrDNA序列分析,初步鉴定此菌为交替假单胞菌(Pseudoalteromonas sp.).该菌对链状亚历山大藻(Alexan-drium catenella)和塔马亚历山大藻(Alexandrium tamarense)有溶藻活性,对锥状斯氏藻(Scrippsiella trochoidea)和中肋骨条藻(Skeletonema costatum)的生长无影响,表明菌株Z3溶藻活性具有种属特异性.通过该菌的菌体悬浮液和除去菌体滤液对链状亚历山大藻实验表明,此菌株具既有直接溶藻作用又有间接溶藻活性. 相似文献
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溶藻细菌MS7的分类鉴定及其溶藻活性的初步研究 总被引：1，自引：0，他引：1
采用形态学、生理生化指标和16SrRNA基因序列同源性分析的方法,对菌株MS7进行鉴定,并通过溶藻试验测定该菌株对铜绿微囊藻(Microcystis aeruginosa)的溶藻活性和溶藻方式。结果表明,MS7菌株为苏云金芽孢杆菌(Bacillus thuringiensis),对铜绿微囊藻具有高效溶藻效果,当菌浓度为108cells/mL,初始藻液叶绿素a浓度为0.7mg/L时,48h溶藻率达到91%。主要通过分泌胞外物质的间接方式溶藻,溶藻物质属于具有很强的热稳定性的非蛋白质类物质。 相似文献
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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
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Mangroves are coastal ecosystems, found in tropical and subtropical regions around the world. They are found in the transitional zones between land, sea, and rivers. Petroleum hydrocarbons are the most common environmental pollutants, and oil spills pose a great hazard to mangroves forests. This research was focused on the isolation and characterization of crude oil‐degrading bacteria from mangrove ecosystems at the Persian Gulf. Sixty‐one crude oil‐degrading bacteria were isolated from mangrove samples (plant, sediment, and seawater) that enriched in ONR7a medium with crude oil as only carbon source. Some screening tests such as growth at high concentration of crude oil, bioemulsifier production, and surface hydrophobicity were done to select the most efficient strains for crude oil degradation. Molecular identification of strains was carried out by amplification of the 16S rRNA gene by PCR. The results of this study were indicated that the quantity of crude oil‐degrading bacteria was higher in the root of mangrove plants compare to other mangrove samples (sediment and seawater). Also, identification results confirmed that these isolated strains belong to Vibrio sp. strain NW4, Idiomarina sp. strain BW32, Kangiella sp. strain DP40, Marinobacter sp. strain DW44, Halomonas sp. strain BS53, and Vibrio sp. strain DS35. The application of bioremediation strategies with these bacteria can reduce crude oil pollution in this important marine environment. 相似文献
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Phytoplankton and bacteria diversity were studied before, during and after red tide phenomena during spring season 2015 in the Eastern Harbour (E.H.) of Alexandria, Egypt. Fifty five species of phytoplankton were identified and represented different distinct classes “Bacillariophyceae; Dinophyceae, Chlorophyceae, Cyanophyceae and Eugelenophyceae”. Also, Diatom formed the most dominant group. The average number of the phytoplankton density varied from 4.8 × 104 to 1.1 × 106 cell l-1 during the study period and Skeletonema costatum was the agent causing the red tide. The existence percentages of bacteria ranged from 2.6 to 17.9% on all media tested. The bacterial isolates on the nutrient agar medium represented the highest existence with a total percentage of 43.6%, followed by MSA medium (25.7%), while the lowest percentage was for the AA medium at 7.8%. However, twelve isolates were selected as representative for bacterial community during study interval. Based on the morphological, biochemical, physiological and enzymatic characteristics, the bacterial strains were described. Depending on the 16S rDNA gene sequence, three common antagonists were aligned as: Vibrio toranzoniae strain Vb 10.8, Ruegeria pelagia strain NBRC 102038 and Psychrobacter adeliensis strain DSM 15333. The interaction between these bacteria and S. costatum was studied. The growth of S. costatum was significantly lower whenever each bacterium was present as compared to axenic culture. More specifically, 30% (v/v) of the all tested bacteria showed the strongest algicidal activities, as all S. costatum cells were killed after two days. 10% of R. pelagia and P. adeliensis also showed significant algicidal activities within six days. 相似文献
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建立螺旋藻转基因体系初报 总被引：9，自引：1，他引：8
Mao Yunxiang 《中国海洋大学学报(自然科学版)》2000,30(Z1):13-18
从钝顶螺旋藻单细胞克隆的制备、重组平台的 克隆、同源重组表达质粒的构建、质粒的电激转化和报告基因的表达等方面对螺旋藻转基因 表达系统进行了研究,初步建立起螺旋藻转基因体系。用次氯酸钠溶液处理获得无菌培养系 ;用钠、钙离子混合液处理,获得了可再生的螺旋藻单细胞。用含EDTA的培养基预培养和用 培养基洗涤可分别去除胞外核酸酶活性和抑制胞内核酸酶活性。以氯霉素乙酰转移酶基因替 换大肠杆菌表达质粒pBV220的抗性选择标记,同时插入系列同源重组片段和萤火虫荧光素酶 基因,构建了同源重组表达载体pBVCS01-04L。电激转化螺旋藻S6-4品系单 细胞,获得了具有稳定氯霉素抗性的培养系,并用SDS-聚丙烯酰胺凝胶电泳证实了报告基 因的表达。 相似文献
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Allelopathic effects of several concentrations of fresh tissue,dry powder and dry tissue of three bloom-forming green macroalgae Ulva pertusa,Ulva linza and Enteromopha intestinalis on the red tide microalga Heterosigma akashiwo were evaluated in microcosms systems.The effects of macroalgae culture medium filtrate were investigated on H.akashiwo using initial or semi-continuous filtrate addition.Preliminary studies on the algicidal effects of one aqueous and four organic solvent extracts from the macroalgae on the microalga were carried out to confirm the existence of allelochemicals in the tissue of these macroalgae.The dry powder of U.pertusa was extracted with methanol,and the methanol extracts were partitioned to petroleum ether phase,ethyl acetate phase,butanol phase and distilled phase by liquid-liquid fractionation.The bioassays of the activity of every fraction were carried out on H.akashiwo.The resultant microcosms assay showed that the growth of H.akashiwo was strongly inhibited by using fresh tissues,dry powder or dry tissue of these three macroalgae,while aqueous and methanol extracts of both macroalgae had strong inhibitory effects on the growth of H.akashiwo,and the EC 50 values for methanol extract of U.pertusa,U.linza or E.intestinalis were 0.016,0.028×10-12 or 0.033×10-12,respectively.While the other three organic solvent extracts（acetone,ether and chloroform） had no apparent effect on its growth,this suggests that the allelochemicals from these three macroalgae had relatively high polarities.The activity of petroleum ether phase,ethyl acetate phase,butanol phase and distilled phase of U.pertusa methanol extract was carried out on H.akashiwo indicating that petroleum ether phase and ethyl acetate phase had stronger algicidal effect on H.akashiwo.The inhibition effect of the ethyl acetate phase was not as strong as that of petroleum ether phase,and effective concentration of petroleum ether phase was 17 mg/L for H.akashiwo.However,no significant algicidal effects were observed on the butanol phase and distilled water phase.These three macroalgae＇s culture medium filtrate exhibited no apparent growth inhibitory effect on the microalga under initial filtrate addition whereas the growth of H.akashiwo was significantly inhibited under semi-continuous filtrate addition,which suggests that continuous release of small quantities of rapidly degradable allelochemicals from the fresh tissue of both macroalgae was effective in inhibiting the growth of H.akashiwo. 相似文献
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海藻工具酶研究Ⅱ.褐藻酸酶的制备、性质及对裙带菜细胞的解离研究 总被引：8，自引：0，他引：8
褐藻酸降解菌埃氏交替单胞菌(Alteromonas espejiana)菌株Al01,通过发酵培养制备褐藻酸酶.该酶作用的最适pH为7.0,最适温度为40℃,最适底物浓度为1%～2%;在离子浓度为0.5mmol/dm3时,Mn2+对酶促反应稍有促进作用,Ca2+、Hg2+则有明显的抑制作用.该酶用于裙带菜单细胞和原生质体解离时,以酶液组成为褐藻酸酶1%、纤维素酶1%,45×10-3的NaC1为渗透剂,酶解温度25℃,pH7.0,酶解3-4h效果最好. 相似文献
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罗氏沼虾(Macrobrachium rosenbergii)幼体新暴发病病原阴沟肠杆菌的分离鉴定 总被引：1，自引：0，他引：1
2010 年, 浙江湖州部分罗氏沼虾(Macrobrachium rosenbergii)育苗场在幼体培育阶段, 暴发 了幼体大规模发病死亡的新病害。从2 个育苗场6 个发病育苗池的发病幼体匀浆液中分离得到6 株 优势生长菌株(编号为NTH01、NTH02、NTH03、316D、316X、316C), 菌落形态较为一致。取代表 菌株NTH01, 以浸泡方式进行人工回感, 结果菌株NTH01 能够导致幼体发病死亡, 且症状与生产表 现一致。经形态学观察、生理生化鉴定、16S rRNA 与gyr B 基因序列系统发育关系构建, 鉴定菌株 NTH01 为阴沟肠杆菌(Enterobacter cloacae).以阴沟肠杆菌omp A 基因片段为靶序列, 建立了PCR 检测方法, 对另外5 株优势菌进行检测, 结果该5 株菌都是阴沟肠杆菌。2011 年, 对4 个发病育苗场 幼体与亲虾进行检测, 结果发病幼体中分离的优势菌检测呈阳性, 亲虾肝胰腺与肠道组织检测到该 菌存在, 但亲虾不表现病症。对30 种抗生素的药敏试验结果表明, 菌株NTH01 对恩诺沙星、氧氟 沙星、庆大霉素等6 种抗生素敏感, 对发病幼体进行针对性用药, 效果明显。本试验结果表明, 阴沟 肠杆菌是导致罗氏沼虾育苗期间幼体大规模发病死亡的致病菌。 相似文献