875 resultados para 16s rRNA sequencing
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A rosy-pigmented Gram-negative, thermophilic bacterium with an optimum growth temperature of about 55degreesC was isolated from Tengchong hot springs in Yunnan province, China. Its growth scarcely occurred below 40degreesC or above 70degreesC. Phylogenetic and secondary structural analyses of 16S rRNA and DNA-DNA hybridization showed that the organism represented a new species of the genus Meiothermus. This new species could be distinguished easily from other species of the genus Meiothermus by the following phenotypic characteristics: rosy pigment, expanded body, sucrose and maltose were not utilized, gelatin and starch were not hydrolyzed. On the basis of the above data, the name Meiothermus rosaceus sp. nov. was proposed for the species represented by the strain RH9901(T)(CCTCC-AB200291). (C) 2002 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
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石爬属鱼类的青石爬和黄石爬的物种界限一直不清楚。采用形态判别和线粒体 16SrRNA基因序列分析相结合的方法 ,分别研究分析了青石爬和黄石爬的物种划分、地理分化及遗传多态性。结果表明 :(1)区别青石爬和黄石爬的重要特征腹鳍起点至臀鳍起点的距离是否大于至鳃孔下角的距离 ,腹鳍相对位置 ,头部相对大小与上颌须的须状延长部分等相互之间有一定的相关性 ,但是在研究的样本中没有截然的界限 ,而是有较大的重叠 ,难以区分 ;(2 )从地埋分布看 ,金沙江不同支流的样本在上述特征上有一定的区别 ,但是没
PCR-DGGE Fingerprinting Analysis of Plankton Communities and Its Relationship to Lake Trophic Status
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Plankton communities in eight lakes of different trophic status near Yangtze, China were characterized by using denatured gradient gel electrophoresis (DGGE). Various water quality parameters were also measured at each collection site. Following extraction of DNA from plankton communities, 16S rRNA and 18S rRNA genes were amplified with specific primers for prokaryotes and eukaryotes, respectively; DNA profiles were developed by DGGE. The plankton community of each lake had its own distinct DNA profile. The total number of bands identified at 34 sampling stations ranged from 37 to 111. Both prokaryotes and eukaryotes displayed complex fingerprints composed of a large number of bands: 16 to 59 bands were obtained with the prokaryotic primer set; 21 to 52 bands for the eukaryotic primer set. The DGGE-patterns were analyzed in relation to water quality parameters by canonical correspondence analysis (CCA). Temperature, pH, alkalinity, and the concentration of COD, TP and TN were strongly correlated with the DGGE patterns. The parameters that demonstrated a strong correlation to the DGGE fingerprints of the plankton community differed among lakes, suggesting that differences in the DGGE fingerprints were due mainly to lake trophic status. Results of the present study suggest that PCR-DGGE fingerprinting is an effective and precise method of identifying changes to plankton community composition, and therefore could be a useful ecological tool for monitoring the response of aquatic ecosystems to environmental perturbations.
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The success of some phylogenetic markers in cyanobacteria owes to the design of cyanobacteria-specific primers, but a few studies have directly investigated the evolution "behavior" of the loci. In this study, we performed a case study in Nostoc to evaluate rpoC1, hetR, rbcLX, and 16S rRNA-tRNA(Ile)-tRNA(Ala)-23S rRNA internal transcribed spacer (ITS) as phylogenetic markers. The results indicated that the gene trees of these loci are not congruent with the phylogeny based on 16S rRNA gene. The mechanisms contributing to the incongruence include randomized variation and recombination. As the results suggested, one should be careful to choose the molecular markers for phylogenetic reconstruction at the intrageneric level in cyanobacteria.
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Although Anabaena is one of the most prevalent planktonic freshwater genus in China, there are few taxonomic reports of Anabaena strains by morphology and genetics. In this study, morphological characteristics and phylogenetic relationships of seven Anabaena strains isolated from two plateau lakes, Lakes Dianchi and Erhai, were investigated. Morphological characteristics such as morphology of filament, cellular shapes and sizes, relative position of heterocytes and akinetes, and presence or absence of aerotopes, were described for these seven strains. Phylogenetic relationships were determined by constructing 16S rRNA gene tree using the neighbor-joining algorithm. The seven strains were morphologically identified as three groups, and phylogenetic analysis based on 16S rRNA gene sequences also showed that these seven strains were in three groups. Strains EH-2, EH-3, and EH-4 were in group A belonging to the Anabaena circinalis and A. crassa group, and strains DC-1, DC-2, and EH-1 were in group B and identified as A. flos-aquae. Strain DC-3 without aerotopes was significantly different from the other isolated strains and was determined as A. cylindrica.
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Two strains of Raphidiopsis Fritsch et Rich were isolated from a fishpond in Wuhan city, China and rendered axenic, and characterized by a combination of morphological, physiological, biochemical and genetic methods. Morphologically the strains were identified as Raphidiopsis mediterranea Skuja (straight trichomes) and R. curvata Fritsch et Rich (coiled trichomes). These two strains demonstrated slight differences in optimal temperature range and GC content, while sharing some common characteristics including inability to grow hetertrophically, similar salinity tolerance (up to 0.78%) and an identical fatty acid composition. Cyanotoxins were not found in the strain of R. mediterranea, however, the strain of R. curvata contained both deoxycylindrospermopsin and cylindrospermopsin. Phylogenetic affiliations inferred from 16S rRNA gene sequences demonstrated that both Raphidiopsis strains clustered with Cylindrospermopsis, demonstrating their phylogenetic ties to Nostocaceae. (c) 2007 Elsevier B.V. All rights reserved.
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The ribosomal RNA molecule is an ideal model for evaluating the stability of a gene product under desiccation stress. We isolated 8 Nostoc strains that had the capacity to withstand desiccation in habitats and sequenced their 16S rRNA genes. The stabilities of 16S rRNAs secondary structures, indicated by free energy change of folding, were compared among Nostoc and other related species. The results suggested that 163 rRNA secondary structures of the desiccation-tolerant Nostoc strains were more stable than that of planktonic Nostocaceae species. The stabilizing mutations were divided into two categories: (1) those causing GC to replace other types of base pairs in stems and (2) those causing extension of stems. By mapping stabilizing mutations onto the Nostoc phylogenetic tree based on 16S rRNA gene, it was shown that most of stabilizing mutations had evolved during adaptive radiation among Nostoc spp. The evolution of 16S rRNA along the Nostoc lineage is suggested to be selectively advantageous under desiccation stress.
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Several recent molecular phylogenetic studies of the sisorid catfishes (Sisoridae) have challenged some aspects of their traditional taxonomy and cladistic hypotheses of their phylogeny. However, disagreement with respect to relationships within this family in these studies highlights the need for additional data and analyses. Here we subjected 15 taxa representing 12 sisorids genera to comprehensive phylogenetic analyses using the second intron of low-copy nuclear S7 ribosomal protein (rpS7) gene and the mitochondrial 16S rRNA gene segments both individually and in combination. The competing sisorid topologies were then tested by using the approximately unbiased (AU) test and the Shimodaira-Hasegawa (SH) test. Our results support previously suggested polyphyly of Pareuchiloglanis. The genus Pseudecheneis is likely to be nested in the glyptosternoids and Glaridoglanis might be basal to the tribe Glyptosternini. However, justified by AU and SH test, the sister-group relationship between Pseudecheneis and the monophyletic glyptosternoids cannot be rejected based on the second intron of rpS7 gene and combined data analyses. It follows that both gene segments are not suitable for resolving the phylogenetic relationships within the sisorid catfishes. Overall, the second intron of rpS7 gene yielded poor phylogenetic performance when compared to 16S rRNA gene, the evolutionary hypothesis of which virtually agreed with the combined data analyses tree. This phenomenon can be explained by the insufficient length and fast saturation of substitutions in the second intron of rpS7 gene, due to substitution patterns such as frequent indels (insertion/deletion events) of bases in the sequences during the evolution.
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Phylogenetic relationships within Metapenaeopsis remain largely unknown. The modern revision of the genus suggests that the shape of the petasma, followed by the presence of a stidulating organ, are the most important distinguishing taxonomic features. In the present study, phylogenetic relationships were studied among seven Metapenaeopsis species from the Indo-West Pacific based on partial sequences of mitochondrial 16S rRNA and cytochrome c oxidase I (COI) genes. Mean sequence divergence was 6.4% for 16S and 15.8% for COI. A strikingly large nucleotide distance (10.0% for 16S and 16.9% for COI) was recorded between M. commensalis, the only Indo-West Pacific species with a one-valved petasma, and the other species with a two-valved petasma. Phylogenetic analyses using neighbor-joining, maximum parsimony, and maximum likelihood generated mostly identical tree topologies in which M. commensalis is distantly related to the other species. Two clades were resolved for the remaining species, one with and the other without a stridulating organ, supporting the main groupings of the recent taxonomic revision. Results of the present study also indicate that the deep-water forms represent a relatively recent radiation in Metapenaeopsis.
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A Gram-positive, aerobic, non-motile, mesophilic strain, djl-6(T), able to degrade carbendazim, was isolated from a carbendazim-contaminated soil sample from Jiangsu province, China. The taxonomic position of this isolate was analysed by using a polyphasic approach. Chemotaxonomic analysis including peptidoglycan type, diagnostic sugar composition, fatty acid profile, menaquinones, polar lipids and mycolic acids showed that the characteristics of strain djl-6(T) were in good agreement with those of the genus Rhodococcus. DNA-DNA hybridization showed that it had low genomic relatedness with Rhodococcus baikonurensis DSM 44587(T) (31.8%), Rhodococcus erythropolis DSM 43066(T) (23.8%) and Rhodococcus globerulus DSM 43954(T) (117.7%), the three type strains to which strain djl-6(T) was most closely related based on 16S rRNA gene sequence analysis (99.78, 99.25 and 98.91% similarity, respectively). Based on the phenotypic properties and DNA-DNA hybridization data, strain djl-6(T) (=CGMCC 1.6580(T) =KCTC 19205(T)) is proposed as the type strain of a novel Rhodococcus species, Rhodococcus qingshengii sp. nov.
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线粒体是细胞内提供能量的细胞器,并负责调节细胞的程序化死亡。因遗传 缺陷引起的线粒体功能障碍会导致ATP 合成障碍、能量产生不足而出现一系列 病症。线粒体DNA 相关疾病目前日益受到广泛的关注,然而在线粒体DNA 相 关疾病领域常用的病例对照法容易受到遗传背景、群体分层、数据质量等方面因 素的影响以致经常得到假阳性结果。系统发育分析方法有助于解决这些方面的问 题,因此我们以此分析方法开展了如下工作: 首先我们对线粒体DNA C1494T 突变及其所属单倍型类群和氨基糖苷类药 物性耳聋之间的关联进行了研究。之前有研究报道了两个中国氨基糖苷类药物性 耳聋的家系,经过对先征者的线粒体DNA 全序列测定在这两个家系中都发现了 C1494T 突变。我们采用系统发育方法分析这两个家系先征者的全序列后,发现 这两个个体都属于线粒体单倍型A。巧合的是,在我们之前的研究中,在一个来 自武汉的汉族样本WH6980 中也有C1494T 突变,而且该个体同样也属于单倍型 类群A。这不由得使人想到:C1494T 突变可能是单倍型类群A 中一个分支的界 定位点,或者,受母系遗传背景的影响,该突变偏好于在A 类群中发生。那么 很有可能单倍型类群A对能够引发氨基糖苷类药物性耳聋的C1494T 突变的发生 有促进作用。 为了验证这个假设,我们从三个省份随机选取了553 个正常个体来检测 C1494T 突变,以调查该突变在普通人群中的发生频率。另外,我们从1823 个中 国人样本中筛选出属于单倍型类群A 的111 个体,在这111 个个体中检测C1494T 突变,以调查该突变是否为单倍型类群A 特有的变异位点。我们的结果表明: 在553 个随机样本群中没有检测到C1494T 突变,这说明该突变是一个稀有的突 变,在正常人群中发生的频率极低。另外,在111 个属于单倍型类群A 的样本 群中,我们也没有检测到C1494T 突变的存在,这说明该突变并非单倍型类群A 特有的变异位点。经过对带有C1494T 突变的全序列进行综合的系统发育学分析 表明,这三条序列的C1494T 突变应是来源于同一次突变事件。同时,根据序列 之间共享变异位点的状况推断,两个耳聋家系具有很近的母系亲缘关系,我们推 测这两个家系的C1494T 突变是来源于一位共同的近期母系祖先。综合这些结果 表明,C1494T 突变的发生与单倍型类群即母系遗传背景没有相关性,是属于在人群中频率极低的散发性突变。 我们又将系统发育分析的方法应用于肿瘤相关的线粒体DNA 突变的研究 中。线粒体在细胞的自由基产生以及细胞凋亡中扮演重要角色;有研究报道线粒 体功能的缺陷能导致癌症的发生,同时又有很多报道指出癌变组织的线粒体基因 组存在异常。为探讨癌组织中线粒体基因组的变异情况及其在癌症的发生和发展 中所扮演的角色,我们选取乳腺癌早期患者为研究对象。 近年来,有大量的研究都报导了在癌组织中存在高频率高密度的线粒体 DNA 体细胞突变,并认为这些突变在肿瘤发生过程中可能具有功能相关性。但 这些研究存在着不可回避的问题,总结来讲归为三个方面:①数据质量差:很多 前面报道的突变数据,经系统发育分析,发现存在不少因样本交叉污染所造成的 假阳性突变。②所测片断太短。大多数研究只是检测了D-loop 区,只占了整个 基因组的约十六分之一,很难全面反映问题。③对照设置有问题,许多研究进行 简单的case-control 分析,忽略了不同个体间母系遗传背景的差异,导致大量假 阳性突变的产生。 针对以上问题的存在,我们基于系统发育分析的方法在中国的乳腺癌病人中 开展了一项研究。分别取得10 例乳腺癌早期患者的癌组织、癌旁组织、以及远 端正常组织;提取了总DNA,对每一份组织样品进行线粒体全基因组测序。这 样做有两个研究目的:第一是调查在严格的质量控制手段下,排除交叉污染所造 成的假阳性突变后,在癌症病人中是否仍然能观察到高频率高密度的线粒体 DNA 体细胞突变。第二个目的是调查中国乳腺癌患者线粒体DNA 体细胞突变情 况,为乳腺癌早期诊断提供有效的信息。 为了避免过去部分研究中出现的问题,我们采取了相应的措施。首先是在严 格的质量控制下,我们对同一个病人的三种不同组织,即癌组织,癌旁组织,正 常组织中的线粒体基因组进行全序列测定的方式来检测体细胞突变。同时将所测 得线粒体全基因组序列进行系统发育的分析;结果表明属于同一个病人的不同组 织都能忠实的聚到一支,而且每一条全序列都完整的带有所属单倍型特有的界定 位点,不存在任何样本交叉或者污染的情况;这样进一步确证了我们数据的可靠 性。同时经过这样的比较,可以非常清晰的筛选出在某一种组织类型中所发生的 体细胞突变。来自10 例病人的癌组织,癌旁组织和正常组织的29 条(7#患者远端正常组 织没有得到)线粒体基因组全序列中,我们只检测到了两个体细胞突变(T2275C 和A8601G)。这两个突变经PCR 克隆试验的验证,在远端正常组织中均不存在, 是真实的体细胞突变。突变A8601G 同时出现在3#患者的癌组织和癌旁组织中; 提示线粒体DNA 的体细胞突变可能先于细胞的癌变,这可能对乳腺癌的早期临 床诊断具有一定的意义。突变T2275C 只出现在6#患者的癌组织中,该突变位于 16S rRNA 基因非常保守的位点上,我们对该突变位点潜在的生物学作用作了进 一步的讨论。 在我们研究的病例中体细胞突变的比率要远远低于先前的报道;造成差异的 主要原因可能是因为我们采取了严格的质量控制手段。综合我们的研究结果表 明,先前所报道的乳腺癌组织中的线粒体基因体细胞突变的频率存在被高估的现 象。目前线粒体突变与肿瘤发生的关系还有待于更深入的研究,同时我们呼吁本 领域的研究要加强数据质量的可靠性。我们的研究表明,系统发育的分析方法在 线粒体DNA 相关疾病的研究中是有效的,因此我们推荐在线粒体DNA 相关疾 病的研究中进行推广。
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本研究采用直接测序的方法,研究了铃蟾属(两栖纲:无尾目:铃蟾科)的 分子系统发育关系及系统学问题。我们测定了我国铃蟾属5 个种共22 个样本的 线粒体DNA 部分片段的序列,包括12S rRNA, 16S rRNA, ND4-tRNALEU 以 及细胞色素b 共四个基因片段,欧洲铃蟾、花铃蟾以及B. pachypus 的相应序列 通过GenBank 获得。利用MrBayes 3.0b4 和 PAUP* 4.0b10 软件对系统发育关系 进行了重建(贝叶斯推断法,最大简约法,最大似然法和邻近法),分析结果表 明,铃蟾属可分为两大支系,一支包括利川铃蟾及中国西南部铃蟾(微蹼铃蟾、 强婚刺铃蟾、大蹼铃蟾);另一支包括东方铃蟾,花铃蟾、欧洲铃蟾以及Bombina pachypus,从分子水平上支持了铃蟾属内不同亚属的划分。我们的结果拒绝东方 铃蟾起源于大蹼铃蟾的假设,同时表明:相对于东方铃蟾,欧洲铃蟾与花铃蟾间 的关系更近。利川铃蟾的有效地位得到支持,中国西南部3 种铃蟾 (微蹼铃蟾、 强婚刺铃蟾、大蹼铃蟾)在所有系统树中形成一个单系,利川铃蟾与之形成姐妹 群。根据我国西南部3 种铃蟾间的很小的遗传差异,以及以往的形态学研究和核 型研究的证据,我们认为将微蹼铃蟾、强婚刺铃蟾归入大蹼铃蟾可能更为合适。 分化时间估计表明,铃蟾属两个亚属的分化发生在3.08–9.16 MYA,我们推测秦 岭的抬升以及同时期青藏高原的上升是铃蟾属内产生亚属分化的主要原因。
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维生素C生产废水有机物浓度高、成分复杂、排放量大,是一种亟待处理的典型工业废水。本研究分别采用实验室规模和中试规模的升流式厌氧颗粒污泥床反应器(UASB)对该制药工业废水的厌氧生物处理工艺进行了较为深入的研究。同时采用两种不依赖于纯培养的分子生物学手段—变性梯度凝胶电泳(DGGE)和扩增核糖体DNA限制性分析(ARDRA)技术揭示了UASB反应器不同运行阶段污泥中微生物群落多样性组成及变化。此外,首次研究了零价铁(Fe0)在厌氧消化过程中对反应器运行及微生物群落结构的影响。 采用城市污水处理厂厌氧消化池絮状污泥和处理啤酒废水的颗粒污泥混合接种,小试中温(35±1℃)UASB反应器在其运行的第65天启动成功。反应器稳定运行阶段,在进水COD浓度为9000mg/L、水力停留时间为12h、容积负荷为13.6 kgCOD/m3.d条件下,其COD去除率稳定在85~90%之间,沼气产率达到4.5 m3/m3.d,沼气甲烷含量平均为72%。中试UASB反应器的接种污泥为厌氧消化污泥,其启动时间相对较长,为90天。在稳定运行期,反应器的进水COD浓度为8000~10000mg/L,水力停留时间和容积负荷分别保持在12~16h和10.6~14.2 kgCOD/m3.d范围,该阶段反应器的平均COD去除率稳定在85%左右,沼气产率平均为5.2m3/m3.d,沼气中甲烷含量为69%。上述结果表明中温UASB工艺用于维生素C生产废水处理是高效、可行的。 与对照反应器相比,添加Fe0的小试UASB反应器的COD去除率和沼气产量分别提高了6.5%和10.2%。同时,磷酸盐平均去除率为79%,比对照提高了64%,目前尚未见类似研究报道。在中试规模的UASB反应器中补充一定量的Fe0可缩短反应器启动时间,促进颗粒污泥的形成,该结果可能具有重要的应用价值。培养试验进一步表明,Fe0可以作为产甲烷菌还原CO2生成甲烷的电子供体。培养实验还表明,当系统中存在硝酸盐(0.40 mM)和硫酸盐(0.26 mM)时,Fe0促产甲烷过程受到一定程度的抑制。 采用细菌通用引物968F/1401R和341F/907R获得的PCR-DGGE指纹图谱均表明UASB反应器不同运行阶段细菌种群结构变化明显。小试和中试稳定期污泥的微生物多样性均高于各自初始接种污泥。产甲烷菌通用引物340F/519R的PCR-DGGE结果显示,虽然接种污泥中产甲烷菌的丰富度系数略低于稳定期,但总体而言,反应器运行期间产甲烷菌的种群组成相对稳定。 通过构建不同处理和不同运行阶段污泥样品的16S rRNA基因文库并对克隆基因进行限制性内切酶消化、测序分析。结果表明,稳定期两个反应器微生物群落结构相似,但与各自接种污泥差异明显。小试UASB反应器接种污泥中细菌的优势菌群分别为变形菌纲的δ亚纲(28.7%)和β亚纲(17.4%),至稳定运行期则演替为革兰氏阳性低GC菌群(21.9%)和变形菌纲的δ亚纲(14.0%)。中试反应器接种污泥Green non-sulfer bacteria(25.9%)和变形菌纲的δ亚纲(16.4%)类群占优势,而稳定期Green non-sulfer bacteria类群(17.9%)、革兰氏阳性低GC菌群(16.2%)和变形菌纲的δ亚纲(15.4%)为优势菌群。 产甲烷菌的优势克隆为SRJ 230、SRJ 26和SRJ 583,前两者分别与Methanosaeta concilii和未培养的Methanobacteria-like克隆Gran7M4的同源性达到97%和98%,后者与Methanomethylovorans. sp同源性为99%。接种污泥中上述类群占总克隆数量的比例较低。小试、中试接种污泥中产甲烷菌分别占7.8%和3.0%,但稳定运行期,该比例明显增加,分别达到21.9%和18.8%。上述结果表明启动期与稳定期污泥产甲烷菌种群组成相对稳定,但各类群数量明显增加。 添加Fe0的UASB反应器稳定运行期污泥中产甲烷菌比例(31.2%)高于对照反应器(24.2%), 革兰氏阳性低GC类群、变形菌纲的δ亚纲比例差异不明显,而变形菌纲β亚纲(6.0%)和Green non-sulfer bacteria(9.2%)的比例均分别低于对照反应器(13.1%和17.1%)。该结果表明,添加Fe0使反应器内微生物群落多样性发生了显著变化。 此外,在添加Fe0的UASB反应器中检测到特异性的克隆SRJ 341和SRJ 320,两者分别同磷酸盐去除和铁氧化有关的克隆子Orbal D41和Clone195的序列相似性达95%和96%。这两个类群可能分别与磷酸盐去除及铁促产甲烷作用密切相关。这一结果尚未见报道。