微生物鉴定系统在肠道病原菌检测中的应用

目的建立简便、快速、系统的病原菌生化检测方法。方法通过应用ATB微生物鉴定系统对112株可疑肠道病原菌菌株进行检测分析,并与国家标准法结合鉴定。结果ATB微生物鉴定系统在112株可疑肠道病原菌菌株中检测出肠道病原菌66株,鉴定结果与国家标准法结果一致,而对常规检测不能确定的37菌株也能给出明确的鉴定结果。结论该系统操作简便、快速,缩短了鉴定周期,提高了鉴定效率,检测范围广,可以作为肠道致病菌检测常规方法的辅助工具,有利于病原菌的快速检出。     

Excel在微生物培养条件优化中的应用

根据正交试验设计的原理,采用Microsoft Excel软件编制优化微生物培养条件的程序,并以实例说明了该程序的使用方法。结果表明,用户只需输入试验的原始数据,即可快速、准确地进行直观分析和方差分析,并可根据极差值得出最佳工艺条件,从而大大提高微生物发酵的效率。     

Root-colonization ability of antagonistic Streptomyces griseoviridis

Root-colonization ability of Streptomyces griseoviridis was tested on turnip rape (Brassica rapa subsp. oleifera) and carrot (Daucus carota) by the plate test and the sand-tube method. In the plate test, colonized root length of total root length was highly significantly greater for turnip rape roots (72%) from those for carrot roots (1%). In the sand-tube method, root-colonization ability was examined in nonsterile soil, and no water was added after sowing. Seeds were treated with spores of S. griseoviridis or the biofungicide Mycostop. Roots were cut into 2-cm segments, and the root segments and the rhizosphere soil were studied separately. Root-colonization frequencies and population densities of the microbe in the rhizosphere soil indicated that S. griseoviridis successfully colonized turnip rape but weakly colonized carrot. Root-colonization of turnip rape is accounted for as proliferation of S. griseoviridis in the rhizosphere of turnip rape seedlings and is not due to the movement of microbe through the rhizosphere by water infiltration.     

刺参海带饲料原料褐藻胶降解菌的分离与鉴定

从海带及刺参养殖环境中筛选有效降解褐藻胶,且对刺参无致病性的微生物,对海带饲料原料进行降解处理,以降低海带饲料中刺参难以消化的褐藻胶成分,显著提高饲料利用率,增加海带原料价值。以褐藻胶为唯一碳源选择培养基初筛;DNS法测定褐藻胶裂解酶酶活;16S r DNA测序及生理生化试验对菌种进行鉴定;高浓度腹腔攻毒试验考察筛选所得菌株对刺参的潜在致病性;分子排阻色谱及高效凝胶色谱法对微生物酶解褐藻胶的终产物进行分析。系统发育树分析表明,菌株WB1与Bacillus amyloliquifaciens有最高同源性,对刺参无潜在致病性;其褐藻胶裂解酶酶解褐藻胶的终产物主要为二糖和三糖,相对含量分别为74.1%和25.9%,平均分子量为516 Da。解淀粉芽胞杆菌WB1可作为一种安全的有益微生物用于刺参海带饲料原料中褐藻胶成分的降解。     

A Review of the Functionality of Probiotics in the Larviculture Food Chain

During the past two decades, the use of probiotics as an alternative to the use of antibiotics has shown to be promising in aquaculture, particularly in fish and shellfish larviculture. This article reviews the studies on probiotics in larviculture, focusing on the current knowledge of their in vivo mechanisms of action. The article highlights that the in vivo mechanisms of action largely remain to be unravelled. Several methodologies are suggested for further in vivo research, including studies on gut microbiota composition, the use of gnotobiotic animals as test models, and the application of molecular techniques to study host–microbe and microbe–microbe interactions.     

Screening of natural compounds with hypolipidemic activity]

In the screening programme for natural hypolipidemic compounds 702 strains of soil microorganisms were tested and 25 of them were selected because of their ability to produce compounds inhibiting sterol synthesis in Hep G2 hepatoma cells. The compounds were estimated in the microbiological model with Tolypocladium inflatum 106 as the test microbe. The 2nd stage of the screening resulted in isolation of 13 strains producing compounds with high hypolipidemic activity, analogous to or higher than the activity of lovastatin in the experimental models.     

Effect of subinhibitory concentrations of antibiotics on catalase activity of plague microbes]

It was shown that the presence of subinhibitory concentrations of ampicillin, cefotaxime or gentamicin in the cultivation medium had a marked inhibitory effect on the catalase activity of plague microbe. The effect depended on the characteristic features of plague microbe strains and the incubation temperature. When the cells of a virulent strain of the plague microbe Y. pestis 1300 were cultivated at a temperature of 37 degrees C on a medium containing the subinhibitory concentrations of ampicillin or cefotaxime, the pathogen virulence for albino mice significantly decreased.     

Stimulation of the respiratory burst of the neutrophils from healthy subjects by different Staphylococcus aureus concentrations

Preopsonized live and heat-killed S. aureus stimulated, without the washing of serum, the luminol-dependent chemiluminescence of human neutrophils obtained from healthy donors. The intensity of chemiluminescence was evaluated by the index of stimulation with staphylococci, with due consideration for their concentration. With the microbe/phagocyte ratio equal to 10:1, these indices had the maximum values when both live and killed staphylococci were used. At high concentrations of staphylococci, especially live ones, all indices were low (those for live staphylococci had negative values) and uniform. As the concentration of the antigen decreased, individual features in the reaction of each donor became apparent. With the microbe/phagocyte ratio equal to 100:1, stimulation with live and killed staphylococci induced the identical fluorescence of neutrophils. The capacity of nonopsonized staphylococci for inducing chemiluminescence was poorly pronounced. For this reason, the test system using S. aureus at low concentrations was proposed for the prognostication of this infection, while the ratio 100:1 can be used for the evaluation of the opsonin-phagocytic system in case of a developed purulent process.     

微生物连续培养模型的最优溢流量控制

本文使用最优控制理论研究了微生物连续培养模型的最优溢流量控制问题,导出了一种关于微生物浓度的线性反馈控制律．在该控制律下,可保证微生物连续培养模型能跟踪理想微生物浓度ｘｄ．     

Chromosomal resistance of plague agent to quinolones]

The nature of increasing chromosomal resistance to quinolones was studied in a model of the plague microbe. Five virulent strains of the natural plague microbe (Y. pestis) were used in the experiment: 363 (1/1479), 231, 2385, 2442 and 2444. The one-stage procedure for isolation of the mutants was applied. It was shown that the frequency of the one-stage mutants resistant to oxalinic acid, pefloxacin and ciprofloxacin amounted to 10(-9)-10(-11) and was 2 to 3 orders of magnitude lower than that of the mutants resistant to nalidixic acid. Two types of the plague microbe mutants resistant to the quinolones were detected: those resistant to the quinolones to the generations (Nalr-phenotype) and those resistant to the representatives of the 3rd generation quinolones (Nals-phenotype). The quinolones were not efficient in the treatment of albino mice with experimental plague caused by the quinolone-resistant forms of the plague microbe.     

深海热液区微生物矿化过程的功能群和分子机制

深海热液区富含铁、锌、铜等含金属矿物(硫化物、氧化物、碳酸盐等)和无机小分子气体(H_2S、H_2、CO_2、CH_4等),具有独特的生态系统。微生物是深海热液生态系统的主要生产者和重要组成,并以控制矿化和诱导矿化两种途径参与了深海热液区的生物地球化学循环。在深海热液区存在着不同类型的微生物参与了生物矿化过程,如硫氧化菌、金属氧化菌、硫还原菌和金属还原菌等。本文详述了这些微生物参与的生物矿化现象、菌群多样性和矿化过程的分子机制,并对研究微生物矿化的研究工作进行了展望。     

Spheroplast bacteriocin from strains of the causative agent of pseudotuberculosis and its identification by the antibacterial activity spectrum and the morphology of the inhibition zones]

Capacity for production of bactericin was found in the spheroplasts of the strains of the rodent pseudotuberculosis microbe. The author named it as pseudotuberculocin. The bacteriocin production was not detected in the initial strains of the pseudotuberculosis microbe. Pseudotuberculocin differed in the antibacterial spectrum and morphology of the growth inhibition zones formed on the plates with the indicator strains from the pesticins produced by the strains of the plaque microbe of the marmot and sandword varieties respectively and the cultures of the plaque microbe from the Transcaucasian Upland, as well as from pesticins of the spheroplasts of these strains. Production of a pesticin differing from pesticins of the rod-like forms of these strains by an ability to inhibit the growth of the homologous indicators was shown in the spheroplasts of the plaque microbe of the marmot and sandword varieties. Sensitivity of the plaque microbe strains of the marmot and sandword varieties to the pesticins of the plaque microbe strains and pseudotuberculocin was noted. With an account of the difference in the activity of the tested pesticins and pseudotuberculocin against the strains of the Frederic collection it is recommended to use this property for identifications of pesticins and pseudotuberculocin.     

静止或缓流污染地表水微生物固定化修复技术研究进展

污染地表水体修复问题是最近几年才被广泛关注的环境保护课题,由于污染地表水体的特殊性,常规修复方法难以发挥高效作用,固定化微生物可以通过提供特殊的微环境,较好地保护优势菌不受土著菌恶性竞争,在保持高效修复能力的同时,可以将优势菌屏蔽于恶劣环境之外,在一定程度上克服了传统修复工艺的不足,具有较好的应用前景.本文概述了微生物固定化技术的特点,分析了利用固定化微生物修复污染环境介质存在的问题和可行性,针对城市静止或缓流污染地表水的特征,指出了将微生物固定化技术移植到污染地表水体修复领域需要解决的的关键技术.     

极端干旱区防护林地土壤微生物多样性

土壤微生物在森林土壤中有重要功能.采用传统培养、脂肪酸鉴定和PCR-DGGE 3种方法分别研究了塔里木沙漠公路防护林地土壤微生物数量、脂肪酸种类和细菌DNA片段的多样性,从微生物学角度为塔里木沙漠公路防护林的管理提供理论依据.结果表明,塔里木沙漠公路防护林的建设促进了风沙土土壤微生物的发育,随着防护林定植年限的增加,土壤微生物数量、脂肪酸和细菌DNA片段的多样性指数明显增大;土壤微生物区系组成中,细菌是优势类群,占微生物总数80%以上,而真菌很少,不到微生物总数1%,但在不同土层间有所差异;传统培养法与现代生物标记和分子生物学方法对塔里木沙漠公路防护林地土壤微生物多样性的研究结果基本一致,说明塔里木沙漠公路防护林的建设使林地土壤生物活性有所增强,有利于林地土壤养分循环与利用.     

广州市空气微生物含量及其变化规律研究

用JWL-IIB新型固体撞击式空气微生物采样仪对广州市18个监测点的空气微生物含量及其月和季节变化势态进行了观察和研究。结果表明：广州市区室外空气微生物年平均含量为2,298cfu／m^3,室内空气微生物年平均含量为1,792cfu／m^3。各功能区的室外空气微生物平均含量（cfu／m^3）大小顺序为：垃圾压缩站（4,573）〉商业步行街（3,835）〉交通枢纽（1,580）〉居民住宅小区（1,413）〉工业厂区（1,197）〉中心公园（1,187）;室内空气微生物含量（cfu／m^3）大小顺序为：交通枢纽（2,511）〉旅游三星酒店（1,699）〉地铁站（1,167）。一年中,市区各监测点室外空气微生物月平均含量变化范围在1,073～4,096cfu／m^3,其中3月份的空气微生物平均含量最高,可达4,096cfu／m^3,而10月份的空气微生物平均含量最低仅为1,073cfu／m^3。四季中,各监测点室外空气细菌和真菌平均含量（cfu／m^3）变化均表现为春季（3,716）〉夏季（2,300）〉冬季（1,816）〉秋季（1,553）。可为广州市区公共场所的卫生防疫和环境治理提供科学依据。     

丛枝菌根真菌对红花根围微生物多样性特征的影响

[目的]研究丛枝菌根(Arbuscular mycorrhiza,AM)真菌对红花根围微生物多样性特征的影响.[方法]对红花接种Glomus mosseae、G.intraradices和混合菌(G.mosseae、G.intraradices、G.cladoideum、G.microagregatum、G.caledonium、G.etunicatum)3种AM真菌,采用传统的平板稀释涂布法对红花根围细菌、真菌、放线菌进行分离、培养、计数和鉴定,并结合单链构象多态性(Single stand conformational polymorphism,SSCP)分析技术对红花根围微生物多样性进行分析.[结果]3处理与对照组红花根围微生物总量表现为G.mosseae＞G.intraradices＞混合菌＞对照,且接种处理红花根围微生物总量显著高于对照.对照组红花各生长期微生物总量均为0-5 cm＞5 cm-10 cm＞10 cm-20 cm,接种处理红花生长至种子成熟期时不同土层微生物数量发生变化,微生物总量为5 cm-10 cm＞0-5 cm＞10 cm-20 cm.聚类分析发现微生物出现接种红花类群与不接种红花类群两大分类类群.[结论]AM真菌从时间和空间上影响了红花根围微生物的多样性特征,对红花农业生产和分析生态系统中微生物之间的相互作用具有重要的理论和实践价值.     

寡核苷酸芯片在微生物检测中的应用

近几年来发展起来的基因组研究技术———基因芯片技术为微生物检测提供了一种强有力的手段。目前国内外已广泛地开展了利用寡核苷酸芯片对多种微生物 (主要是病毒和细菌 ,少量有真菌 )进行相关检测的研究 ,并在对微生物病原体检测、种类鉴定、功能基因检测、基因分型、突变检测、基因组监测等方面获得了成功。由于寡核苷酸探针具有可根据研究需要任意设计、特异性高等特点 ,寡核苷酸芯片在微生物检测中有着巨大的应用价值 ,具有广阔的应用前景。     

洗发、护发化妆品微生物检查方法学研究

为提高化妆品潜在微生物的阳性检出率,建立洗发、护发类化妆品微生物限度和控制菌检查方法。采用常规法、培养基稀释法、薄膜过滤法对4种洗发、护发类化妆品进行微生物限度与控制菌方法学研究。结果显示,飘柔长效柔顺滋养洗发露、海飞丝去屑洗发露、飘柔人参滋养润发精华素、力士密集滋养修复-发膜级精华素菌落总数检测方法分别为0.2 m L/皿法、800 m L/膜法、0.5 m L/皿法和300 m L/膜法;霉菌及酵母菌检测方法分别为300 m L/膜法、300 m L/膜法、1 m L/皿法和1 m L/皿法;除海飞丝去屑洗发露采用培养基稀释法,其他均采用常规法进行控制菌检查。建议在化妆品微生物检验前应进行微生物方法研究,从而提高化妆品"潜在"病原菌的检出率。     

More than words: the chemistry behind the interactions in the plant holobiont

Plants and microbes have evolved sophisticated ways to communicate and coexist. The simplest interactions that occur in plant-associated habitats, i.e., those involved in disease detection, depend on the production of microbial pathogenic and virulence factors and the host's evolved immunological response. In contrast, microbes can also be beneficial for their host plants in a number of ways, including fighting pathogens and promoting plant growth. In order to clarify the mechanisms directly involved in these various plant–microbe interactions, we must still deepen our understanding of how these interkingdom communication systems, which are constantly modulated by resident microbial activity, are established and, most importantly, how their effects can span physically separated plant compartments. Efforts in this direction have revealed a complex and interconnected network of molecules and associated metabolic pathways that modulate plant–microbe and microbe–microbe communication pathways to regulate diverse ecological responses. Once sufficiently understood, these pathways will be biotechnologically exploitable, for example, in the use of beneficial microbes in sustainable agriculture. The aim of this review is to present the latest findings on the dazzlingly diverse arsenal of molecules that efficiently mediate specific microbe–microbe and microbe–plant communication pathways during plant development and on different plant organs.     

（超）高压对微生物的影响及其诱变效应探讨

(超)高压对微生物有多方面的影响,它不仅可使微生物细胞体积形态、细胞组分发生变化,还可使微生物的基因表达和核酸结构及其生物学功能发生改变。(超)高压的这些生物学效应,使其不仅可以应用到食品杀菌、保藏及某些加工过程,而且在微生物菌种诱变方面具有很大的应用潜力。这是因为(超)高压既然可以使核酸发生变化,那么它诱导微生物发生突变就很有可能。现从(超)高压对微生物的影响出发,并结合国内外有关实例及作者的研究工作,初步探讨其诱变育种的可行性。