黄喉拟水龟体表溃疡病原菌SG_(24)的分类鉴定

从患溃疡的黄喉拟水龟病灶中分离到一株病原菌SG24。对菌株SG24进行了常规生理生化测定和ATBExpression半自动细菌鉴定仪鉴定,并测定16S rRNA序列,分析其与相关细菌相应序列的同源性,构建了系统进化树。普通细菌学方法结果显示菌株SG24为黏质沙雷氏菌(Serratia marcescens)。以沙雷氏菌属的16S rRNA基因序列设计一对引物进行PCR扩增,获得了菌株SG24大小约950 bp的16S rRNA部分基因片段,测序结果显示菌株SG24与黏质沙雷氏菌同类,与已登录的黏质沙雷氏菌(S.marcescensDQ207558)的16S rRNA同源性大于99%。综合以上分类鉴定结果,确定菌株SG24属于沙雷氏菌属的黏质沙雷氏菌。药物敏感试验结果表明:菌株SG24对链霉素、庆大霉素、壮观霉素、强力霉素、卡那霉素、阿米卡星、诺氟沙星、氧氟沙星和复方新诺明敏感。     

异育银鲫气单胞菌病原菌鉴定和药敏试验

从患病异育银鲫体内分离到5株可疑菌株,经API 20NE细菌生化鉴定,YCS07-03和YZ07-11株鉴定率为99.2%和99.3%。注射感染中5×108 CFU.mL-1剂量组表现出较强的致病性,12 d死亡率100%。菌株在营养肉汤培养液中呈均匀混浊状;在营养琼脂平皿中呈灰白色半透明菌落;在血琼脂培养基中呈光滑灰白色菌落,YZ07-11株出现透明的β溶血环;在TCBS培养基呈黄色菌落;在SS和麦康凯培养基中形成无色透明的扁平菌落。经负染电镜观察,菌株两端圆,呈直杆状,无芽孢,极生单鞭毛,菌株大小(短径×长径)分别为1.53μm×2.71μm和0.80μm×2.12μm。菌株经生化实验鉴定为温和气单胞菌(Aeromonas sobria)和嗜水气单胞菌(Aeromonas hydrophila)。试验结果表明:菌株对丁胺卡那霉素、头孢噻肟、庆大霉素、左氟沙星、复合磺胺、氟嗪酸、洛美沙星、复方新诺明、链霉素和新霉素均产生高度敏感;对万古霉素为中度敏感;氨苄青霉素、羧苄青霉素、强力霉素和青霉素产生耐药。     

巯基棉吸附氢化物无色散原子荧光法测定痕量硒和碲

试样用硝酸、盐酸和过氯酸分解,以过氯酸消除硝酸,然后制备成10%的盐酸溶液,经巯基棉柱吸附Se和Te,用1∶1硝酸洗脱,于20%盐酸-5%硝酸介质中进行原子荧光测定.经测定,对含Se为0.27ppm的试祥,相对标准偏差为11.2;含Te在1.5ppm的试样,相对标准偏差为8.10,此法测定Se和Te含量范围为0.001-1ppm.     

石油污染土壤生物修复的强化技术

为探索石油污染土壤的高效修复方法,从实验室保存的优势菌中筛选得到4株降油效果最佳菌,采用摇床和恒温培养箱培养,对含油量为5%的石油污染土壤进行微生物菌剂强化处理和环境强化实验.微生物菌剂强化结果表明:4种菌和除油效果最好的A、C、D混合菌3 d可将石油烃依次降解24%、19.81%、22.55%、26.46%、39.67%;并对该菌群的最佳投加配比进行确定,A、C、D菌群数量的最佳配比为NA∶NC∶ND=1∶2∶0.5,3 d内菌群A、C、D在最佳接种配比情况下可将石油烃降解44.2%.环境强化实验结果表明:A、C、D菌群在最佳修复条件营养物质C∶N∶P为75∶8∶3、表面活性剂为0.5%、通气条件为6层纱布、电子受体H2O2的加入量为1.5%下,3 d内石油烃降解61.46%,比自然条件下修复的除油率4.7%提高了56.76%,较只进行菌种强化时最高除油率44.2%提高了约17%.     

49味中药及其复方与抗生素对溶藻弧菌的体外抑菌作用

【目的】筛选对溶藻弧菌(Vibrio alginolyticus)有抑菌作用的中草药及其复方以及抗生素。【方法】采用改良的牛津杯法对诃子、白芍、甘草等49种单味中药进行溶藻弧菌体外抑菌试验,以体外抗菌活性较好的22种药物,按中药配伍规则组成二联、三联复方,采用生药质量浓度分别为60、240 mg/mL的中药进行中药复方体外抑菌试验。用抗生素对溶藻弧菌进行药敏试验。【结果】当单种中药体外抑菌药物质量浓度为240 mg/mL时,诃子、乌梅、醋五味子等对溶藻弧菌抑菌作用明显,为极敏感。在二联中药体外抑菌试验中,当中药质量浓度为60mg/m L时,诃子、乌梅组成复方中药等8种复方对溶藻弧菌协同抑菌作用明显,为极敏感,药物质量浓度在240mg/m L时,诃子与白芍等14种双联中药的协同抑菌作用明显,为极敏感。在三联中药体外抑菌试验中,在药物质量浓度60 mg/mL时,诃子、乌梅、蒲公英等组成24种复方中药按质量比1∶1∶1的抑菌效果极为敏感,药物质量浓度在240mg/m L时,黄芩、诃子、黄芪等22复方中药按质量比1∶1∶1对的抑菌作用明显,为极敏感。溶藻弧菌对恩诺沙星、盐酸多西环素、土霉素及甲氧苄啶/磺胺甲噁唑4种药物高度敏感。【结论】18种单味中药对溶藻弧菌有抑制作用,黄芩、诃子、黄芪等24个三联复方中药药效较强,多个抑菌作用效果良好的三联复方中药可用于鱼病防治研究。     

不同养殖模式虾池弧菌对抗菌药物的耐药性与虾池水质评价

研究了湛江东海岛3种不同养殖模式虾池弧菌对抗菌药物的耐药性,并对虾池水域环境的水温、盐度、DO、pH、叶绿素a、DOC、无机氮、无机磷、硅酸盐、细菌总数和弧菌数量变化进行了监测和评价。结果表明,调查的三个虾池的弧菌对万古霉素产生耐药性,高位新池和传统精养池的弧菌对利福平产生耐药性,对其他抗菌药尚未形成耐性,3个虾池的弧菌对恩诺沙星和氯霉素高度敏感,传统精养池和天然虾池的弧菌对复方新诺明、庆大霉素、TMP和环丙沙星高度敏感;在水平差异上,高位新池的弧菌比传统精养池和天然虾池对12种抗菌药更具耐药性,同时多重耐药菌株在高位新池中出现,可能与虾苗来源和配合饲料中添加了抗菌药物有关。水质监测结果表明,养殖过程中,虾池水域环境逐渐富营养化,无机氮和Chla超过富营养化阈值,细菌总数增加;两个精养池的水体富营养化程度高于天然虾池;调查期间的弧菌数量在对虾发病的感染剂量阈值范围之内,尚无弧菌病害发生的潜在危险。     

红鳍笛鲷弧菌病病原的研究

从广东湛江特呈岛鱼排取患病红鳍笛鲷进行病原分离、纯化,得到一株病原菌Ls 1。该菌 为革兰阴性短杆菌,有运动性,菌落半透明,最适温度28～30℃,需盐生长,氧化酶反应阳性,发酵 葡萄糖不产气,不发酵肌醇,对弧菌抑制剂O/129敏感。经API ID32E细菌鉴定系统及弧菌科细 菌生化鉴定管鉴定,该菌为一株溶藻弧菌(Vibrioaginolyticus);其对红鳍笛鲷的半数致死量为6.32 ×105mL-1。药敏试验结果表明,该菌对阿莫西林、先锋V不敏感,对新生霉素、卡那霉素、多粘菌 素B、四环素中度敏感,而对庆大霉素、氟哌酸、氯霉素、红霉素、链霉素和复方新诺明等有较高的敏 感性。     

凡纳滨对虾烂尾病病原的分离鉴定及药敏分析

【目的】研究广东湛江地区凡纳滨对虾(Litopenaeus vannamei)烂尾病主要病原及其药敏特征。【方法】从对虾病灶部位分离纯化细菌,用2株代表菌株对健康虾进行创伤浸浴感染试验,分析菌株形态特征、生理生化特征以及16S rRNA和HSP60基因序列,以哈维氏弧菌(Vibrio harveyi)和坎氏弧菌(V. campbelli)溶血素基因特异引物扩增菌株基因组DNA,通过纸片扩散法测试菌株对17种药物的敏感性。【结果】从患病亲虾和养殖对虾分别分离获得编号2018B22和2018MZ1的代表菌,两株菌16Sr RNA和HSP60基因序列均与哈维氏弧菌最相似,且均可被哈维氏弧菌溶血素基因引物特异扩增,表型特征亦与哈维氏弧菌相近;两株菌均可引起凡纳滨对虾烂尾病,其中菌株2018B22的致病力较2018MZ1更强,而后者的耐药谱更广。【结论】湛江地区凡纳滨对虾烂尾病主要病原为哈维氏弧菌。     

东太平洋赤道公海茎柔鱼生物学特性

根据2013年4~6月在赤道公海探捕期间采集茎柔鱼样本,研究赤道公海茎柔鱼渔业生物学特性。结果表明,不同性别、不同月份,茎柔鱼胴长和体质量组成不同。雌、雄性样本的胴长范围分别为93~495 mm和94~406 mm,优势胴长组分别为260~340 mm和240~320 mm,分别占样本总数72.53%和70.26%;雌、雄性样本体质量范围分别为25~3 900 g和33~2170 g,优势体质量组分别为400~1 200 g和200~1 000 g,分别占样本总数82.71%和87.82%。雌、雄性茎柔鱼净体质量比例分别介于31.69%~80.51%和37.05%~81.35%之间,平均值分别为60.45%和62.73%。协方差分析表明,茎柔鱼胴长与体质量、胴长与净体质量的生长均存在性别间差异,胴长与体质量的生长都最适合用幂函数表示,而胴长与净体质量的生长,雌、雄性样本分别最适合用幂函数和指数函数表示。不同月份茎柔鱼性别比例构成不同,4月、5月和6月性别比例分别为1.87∶1、1.61∶1和1.17∶1,全部样本的性别比例为1.61∶1。不同月份茎柔鱼性腺成熟度的组成不同。不同性别、不同月份间茎柔鱼胃含物等级组成存在差异。     

盐酸普鲁卡因诱导下海洋真菌Hypocrea lixii次级代谢化学成分

【目的】通过化学诱导方法从一株海洋真菌Hypocrea lixii中获得多样化的活性小分子化合物。【方法】对菌株在盐酸普鲁卡因的化学诱导作用下进行固体发酵,代谢产物采用硅胶减压柱层析、Sephadex LH-20以及pHPLC等手段分离纯化,对化合物运用NMR、MS等波谱学技术并比对文献进行结构鉴定,采用Ellman比色法及DPPH自由基清除法对化合物进行初步抗乙酰胆碱酯酶(AChE)和抗氧化活性测试。【结果】从海洋真菌Hypocrea lixii在盐酸普鲁卡因诱导下的发酵提取物中分离得到4个异黄酮类化合物,包括6'-O-crotonylgenistin(1)、Genistein(2)、Daidzein(3)和Genistin(4),以及对氨基苯甲酸甲酯(5)、对羟基苯丙酸(6)和胞嘧啶(7),其中化合物1和6为该种中首次报道,化合物5为生物转化来源首次报道,化合物2~4可能源自培养基。在100μmol/L剂量浓度下,化合物1~4对AChE的抑制以及DPPH自由基的清除活性均较弱,化合物5和6显示了相对强的AChE抑制活性,抑制率分别为40%和38%。【结论】盐酸普鲁卡因对该菌次级代谢产生了显著的影响,为深入研究该菌株化学诱导次级代谢产物提供基础。     

30种中药及其复方对温和气单胞菌的抗菌作用

为评价中药对温和气单胞菌的体外抑菌效果,取鱼腥草、五倍子、黄芩等30种中药,采用水提法制备药液,通过试管二倍稀释法测定各药液对温和气单胞菌的最小抑菌浓度(MIC)及最小杀菌浓度(MBC),筛选出抗菌作用较强的中药作为主药,与牡丹皮、龙胆草、蒲公英等18种中药组成复方,测定中药复方对温和气单胞菌的体外抑制效果。结果表明:五倍子、山茱萸、白芍对温和气单胞菌有较强抑菌活性(MIC≤12.5mg/mL),选取8种主药与清热凉血、清热燥湿、清热解毒药分别组成复方,其中五倍子、诃子、五味子、乌梅与其他多种中药组成的复方抗菌作用增强。     

波吉卵囊藻对抗生素的敏感性及其无菌化培养

研究了青霉素、链霉素、庆大霉素和卡那霉素对波吉卵囊藻生长的影响,采用4种方法添加抗生素获得无菌藻株,比较波吉卵囊藻除菌前后的生长特点。结果表明:青霉素和链霉素浓度为1000IU/mL时,对波吉卵囊藻生长无明显影响;庆大霉素和卡那霉素浓度达500IU/mL时,对波吉卵囊藻生长无明显影响。微藻培养液中细菌对抗生素敏感性实验表明,除青霉素外,链霉素、庆大霉素和卡那霉素均对藻液中细菌有明显抑制作用。采用4种方法添加抗生素,均可获得无菌藻株。与未除菌时相比,无菌的波吉卵囊藻不易老化。     

A method of batch-purifying microalgae with multiple antibiotics at extremely high concentrations

Axenic microalgal strains are highly valued in diverse microalgal studies and applications. Antibiotics, alone or in combination, are often used to avoid bacterial contamination during microalgal isolation and culture. In our preliminary trials, we found that many microalgae ceased growing in antibiotics at extremely high concentrations but could resume growth quickly when returned to an antibiotics-free liquid medium and formed colonies when spread on a solid medium. We developed a simple and highly efficient method of obtaining axenic microalgal cultures based on this observation. First, microalgal strains of different species or strains were treated with a mixture of ampicillin, gentamycin sulfate, kanamycin, neomycin and streptomycin (each at a concentration of 600 mg/L) for 3 days; they were then transferred to antibiotics-free medium for 5 days; and finally they were spread on solid f/2 media to allow algal colonies to form. With this method, five strains of Nannochloropsis sp. (Eustigmatophyceae), two strains of Cylindrotheca sp. (Bacillariophyceae), two strains of Tetraselmis sp. (Chlorodendrophyceae) and one strain of Amphikrikos sp. (Trebouxiophyceae) were purified successfully. The method shows promise for batch-purifying microalgal cultures.     

一株H_5N_1亚型禽流感病毒株NA基因的克隆与序列分析

用RT-PCR方法从1个H5N1亚型禽流感病毒分离株A/Chicken/Guangdong/DH/1997扩增NA基因cDNA片段,将其克隆至pMD18-T载体,获得重组质粒pMD-NA,并对其核苷酸序列进行测定和分析。结果表明,该毒株的NA基因长度为1350bp,编码449个氨基酸,与其它H5N1亚型AIV分离株的核苷酸序列同源性为97.0%～99.4%,氨基酸序列同源性为97.7%～99.1%,提示禽流感病毒NA基因保守性较高。NA基因氨基酸序列的聚类分析表明该毒株与来自香港的A/Pheasant/HK/FY155/01和A/Ch/HK/FY150/01两个分离株处于同一进化枝,亲缘关系较近。     

Response to selection for fast growth in the second generation of Pacific oyster (Crassostrea gigas)

Mass selection for fast growth was conducted in three Pacific oyster (Crassostrea gigas) stocks from China, Japan and Korea using previously established lines (CS1, JS1, and KS1). To determine whether continuous progress can be achieved by selection for growth, the progeny of three second-generation Pacific oyster lines was selected for shell height and evaluated via a 400-day farming experiment. When harvested at the end of the experiment, the selected crosses of CS2, JS2, and KS2 lines grew by 9.2%, 10.2% and 9.6% larger than the control crosses, respectively. During grow-out stage, the genetic gain of three selected lines was (10.2 ± 1.4)%, (10.4 ± 0.3)%, and (8.4 ± 1.6)%, respectively; and the corresponding realized heritability was 0.457 ± 0.143, 0.312 ± 0.071 and 0.332 ± 0.009, respectively. These results indicated that the selection for fast growth achieved steady progress in the second generation of oyster. Our work provides supportive evidence for the continuity of the Pacific oyster selective breeding program.     

Axenic culture of free-living conchocelis of<Emphasis Type="Italic">Porphyra yezoensis</Emphasis> and<Emphasis Type="Italic">Porphyra haitanensis</Emphasis>

After discarding marine microorganisms from conchocelis of Porphyra yezoensis and Porphyra ha/tanens/s, their axenic cultures were obtained through treatment with antibiotics. Antibiotic disc tests were carried out to determine the effectiveness of each antibiotic in eliminating contaminating microorganisms. Five of 12 antibiotics tested were selected and used to produce the axenic cultures in this study, which showed that 200 μg/mL streptomycin, 250 μg/mL penicillin, 252 μg/mL kanamycin, 30 μg/mL neomycin, 200 μg/mL chloramphenicol were effective concentrations for eliminating microorganisms from conchocelis when antibiotics were added singly step by step; whereas simultaneous combination of 150 μg/mL streptomycin, 250 (or 350) μg/mL penicillin, 150 (or 250) μg/mL kanamycin, 70 μg/mL neomycin and 200 μg/mL chloramphenicol was also effective for producing the axenic cultures. However,it seemed that the treatments with antibiotics applied individually were more feasible than those with all antibiotics added at the same time. This may be due to the combined inhibiting effect of antibiotics on the growth and development of conchocelis.     

The preparation and antioxidant activity of glucosamine sulfate

Glucosamine sulfate was prepared from glucosamine hydrochloride that was produced by acidic hydrolysis of chitin by ion-exchange method. Optical rotation and elemental analysis characterized the degree of its purity. In addition, the antioxidant potency of chitosan derivative-glucosamine sulfate was investigated in various established in vitro systems, such as superoxide (O-2)/hydroxyl (·OH) radicals scavenging, reducing power, iron ion chelating. The following results are obtained: first, glucosamine sulfa...