中国7个毛木耳(Auricularia polytricha)菌株ITS序列比较

对毛木耳7个菌株rRNA基因内转录间区(ITS)进行了克隆测序,并将其与木耳属其它几种的相应序列进行了比较.在供试的7个毛木耳菌株中,除特大(209bp)外,其余6个菌株的ITS2区序列长度完全相同;毛木耳rRNA基因的两个ITS区序列有一定数量的碱基变异,整个ITS区共有11个变异位点.与下载的木耳属另外4个种相比较,均有较大程度的变异.根据遗传同源性分析,遗传距离分析和系统树上所显示的供试菌株及相关已知种的亲缘关系,ITS序列分析支持传统的依据形态学进行的木耳属分类.图2表2参9     

云南会泽废弃铅锌矿区植物丛枝菌根和深色有隔内生真菌研究

用碱解离、酸性品红染色法对云南省会泽县者海镇废弃铅锌矿区的17科21种植物的丛枝菌根状况进行了调查,结果发现,15种植物形成典型的丛枝菌根,占所调查植物的71%;2种植物不确定是否形成丛枝菌根,占所调查植物的10%;4种植物没有形成丛枝菌根,占所调查植物的19%.用湿筛沉淀法从这些植物根际土壤中共分离鉴定出了4属20种丛枝菌根真菌(AMF),即无梗囊霉属(Acaulospora)4种,球囊霉属(Glomus)14种,巨孢囊霉属(Gigaspo-ra)1种,盾巨孢囊霉属(Scutellospora)1种;其中,球囊霉属分离频率为77%,是样地的优势属.在AMF中,疣突球囊霉(G.verruculosum)分离频率最高,在20种植物的根际土中都有发现;此外,聚生球囊霉(G.fasciculatum)的相对多度最大,为56%,具有最强的产孢能力.同时,在13种植物的根中发现了深色有隔内生真菌(DSE),占调查植物的62%,其中,10种植物同时被DSE和AMF感染.本调查研究表明,AMF和DSE能普遍存在于Pb、Zn重金属污染土壤中.     

利用rep-PCR研究云南尼泊尔桤木根瘤内Frankia基因多样性

利用rep-PCR指纹技术对云南5个地区的尼泊尔桤木根瘤内Frankia菌基因多样性进行研究,实验发现Frankia菌呈现丰富的基因多样性.所有71个样品被分为11种不同的基因类型.除高黎贡山外,不同地域都有某种基因型占优势,显示Frankia菌基因型与地域有紧密关系.所观察的5个地区中,高黎贡山Frankia菌基因型种类最多,多样性指数最高,基因多样性最为丰富.结合高黎贡山地理资料及其它生物多样性相关研究,推测与高黎贡山尼泊尔桤木共生的Frankia可能作为种储备库,为其它地区的寄主植物提供了祖先菌株.图8表1参13     

粘细菌的活性检测及与环境因子的相关性

为筛选具有抗菌活性的粘细菌,利用兔粪诱导、大肠杆菌划线诱导和滤纸诱导3种方法从内蒙古凉城地区采集的20种土样中分离粘细菌,结合形态观察、生理生化特征和分子鉴定方法确定这些菌株的分类地位,通过平板对峙法分析抗菌活性,并采用统计学方法分析其与环境因子的相关性.共分离得到140株菌,包括39株纯粘细菌,经鉴定分别为黄色粘球菌(17株)、橙色粘球菌(13株)、变绿粘球菌(5株),还有4株只鉴定到粘球菌属(Myxococcus sp.).抗菌结果显示:39株纯菌均表现出可以对一种甚至多种指示菌产生抗性,其中37株抑制大肠杆菌的生长,35株抑制马铃薯晚疫病菌的生长,26株抑制金黄色葡萄球菌的生长,20株抑制酿酒酵母菌的生长,19株抑制枯草芽孢杆菌的生长.在分析环境因子与粘细菌分布情况的关系时发现,分离出的溶细菌类群的菌株数、溶纤维素类群的菌株数及总的菌株数与土壤p H和速效钾的含量呈正相关,与含水量呈负相关,与其它参数无明显相关性.综上,内蒙古凉城地区粘细菌的优势菌群为粘球菌属,且绝大多数都有不同程度的抗菌活性;结果可为丰富内蒙古地区粘细菌资源及抗马铃薯晚疫病农药研发奠定基础.     

河南省不同类型土壤可培养放线菌多样性及拮抗活性菌株筛选

分别从河南省濮阳、南阳、信阳、三门峡和商丘等地区采集潮土、黄棕壤、水稻土、褐土、盐碱土等土壤样品45份,采用8种不同的分离培养基对土壤放线菌进行分离和培养;通过16S rRNA基因序列分析对可培养放线菌进行分类鉴定;以7种植物病原菌为靶标,通过对峙培养筛选拮抗活性菌株,并对具有拮抗活性菌株的次级代谢产物合成相关基因进行初步筛查.结果表明,从5种类型土壤中分离得到放线菌分离物955株,分布于放线菌门的10个目12个科17个属,包含626个物种,其中9个分离物为潜在的新种;分离物中链霉菌属菌株751株,占分离菌株的78.64%,为最主要的优势菌属,稀有放线菌204株,占21.36%;不同类型土壤放线菌的分离频率存在一定的差异,其中褐土分离的放线菌数量最多,水稻土的分离数量最少,但是各类型土壤分离的可培养放线菌在属水平上差异不大;筛选获得对植物病原菌有拮抗活性的菌株392株,占总分离物的41%,其中链霉菌332株,占总拮抗活性菌株的84.7%,稀有放线菌60株,占总拮抗活性菌株的15.3%,且多数活性菌株含有多种生物活性物质合成相关的功能基因.由此可见,河南省土壤放线菌多样性丰富,并蕴藏丰富的稀有放线菌和拮抗活性放线菌资源,具有发掘放线菌新物种和新活性化合物的潜力.(图4表6参33附表1)     

油菜根肿休眠孢子间接酶联免疫检测法的建立

根肿病是由专性寄生菌--芸苔根肿菌感染所引起的一种严重影响十字花科植物生长的植物病害.本文针对根肿病缺乏简便、快速检测方法的问题,制备油菜根肿休眠破碎孢子抗血清,确定抗血清及酶标抗血清最佳工作浓度,优化间接酶联免疫反应条件;优化的抗血清和酶标血清的工作浓度分别为1:2000和1:1000,孢子的饱和包被浓度为107个/mL.确定休眠孢子稀释液的最低检测浓度为10个/mL,建市快速检测油菜根肿菌的间接酶联免疫吸附测定法,该方法稳定、可靠,板间误差和板内误差均小于10.0%.与9种土壤分离得到的真菌和7种土壤常见菌黑曲霉、粉红粘帚霉、立枯丝核菌、产黄青霉、绿色木霉、枯草杆菌、脓杆菌进行特异性实验,其中一种未知菌M1交叉反应率>30%,其余在8.51%～24.88%之间,真菌的交叉反应率普遍高于细菌.对已知孢子浓度的土壤进行了检测,土壤样品休眠孢子浓度的最低检测限度为103个/g.     

广西涠洲岛沉凝灰岩土壤粘粒矿物的研究

用X射线衍射分析和电子显微镜分析,对涠洲岛沉凝灰岩母质发育土壤的两个典型剖面八个土样的粘粒矿物进行分析研究。结果表明,离火山口距离不同的两个剖面土壤粘粒矿物组成不同,1号剖面以2:1型粘粒矿物为主,2号剖面则以1:1型粘粒矿物为主;结合其它分析结果,讨论了两个剖面土壤粘粒矿物组成不同的原因、对土壤有关特性的影响及其与土壤形成和分类的关系。     

水葫芦内生细菌脂肪酸生物标记特性研究（Characteristics of PLFA Biomarkers for the Endophyte Bacteria inside Eichhornia crassipe（Mart.）Solms）

应用基于微生物细胞脂肪酸成分鉴定的全自动微生物鉴定系统,鉴定水葫芦内生细菌25株,分属15个属.共检测到27个脂肪酸生物标记(PLFAs),这些生物标记分为4种类型,即(1)高频次分布:在25株细菌中出现13～22次,属于细菌总体类群(general)的生物标记.(2)中频次分布:在25株细菌中出现5～7次,可以用于代表细菌属类群(genus)识别生物标记.(3)低频次分布:在细菌中的分布概率较小,可以用于指示特定细菌种间差异的生物标记.(4)微频次分布:仅在一种细菌种类出现,是细菌种(species)特征生物标记.利用脂肪酸生物标记分析同属细菌不同种的差异,可将微杆菌属分为2类,第1类包括菌株9Microbacterium barkeri和11Microbacterium imperiale,这两个菌株17:0ISO和14:0ISO的脂肪酸生物标记含量均为0.第2类包括10Microbacterium esteraromaticum、12Microbacterium lacticum和13Microbacterium liquefaciens,这3个菌株均含有17:0ISO脂肪酸生物标记而区别于第一类菌株.利用脂肪酸生物标记的差异对25株内生细菌进行聚类分析,可将水葫芦内生细菌类群分为4类.不同植物内生菌群落中存在着特异的生物标记,利用特征脂肪酸生物标记的分析方法,分析水葫芦内生细菌的群体特性,对于植物内生菌微生物群落的研究具有重要意义.     

链格孢菌菌株致病性及其遗传差异性

对分离自紫茎泽兰的19个链格孢菌菌株的致病性进行了比较研究，并对这19个菌株和其它来源的3个菌株的5．8S rDNA及其两侧的ITS1区和ITS2区进行了序列分析．结果显示，链格孢菌菌株的致病性差异明显；21株链格孢菌菌株在5．8SrDNA及其两侧的转录问区（ITS区）的序列无差异，而与百日草链格孢菌（Alternaria zinnine）的序列差异显著，表明21株链格孢菌菌株属种内变异．采用AFLP分子标记技术对21株链格孢菌的DNA扩增片段长度多态性进行了分析，结果表明，链格孢菌自然变异群体内存在很高的遗传多样性．链格孢菌菌株的相似性与菌株的地理来源有一定的相关性，但基于AFLP标记划分的AFLP类群与基于寄主病情指数划分的致病力类群问关系不相一致；起始菌株与变异菌株相似性显著，但二者和致病性的关系不显著．图2表1参18     

不同生境产脂肪酶菌株的筛选及多样性

为发掘不同特性脂肪酶微生物资源,采用纯培养方法从青海高寒草地、雅安山区、成都平原分离得到产脂肪酶菌株54株.通过对菌株的DNA进行ERIC-PCR指纹图谱分析,按聚类树划分为5个操作分类单元.16S rDNA序列测定和聚类分析显示,分离菌株分布于芽孢杆菌属(Bacillus)、克雷伯氏菌属(Klebsiella)、假单胞菌属(Pseudomonas)、葡萄球菌属(Staphylococcus)、肠杆菌属(Enterobacter).多样性分析表明,与青海高寒草地、雅安山区相比,成都平原产脂肪酶菌株遗传多样性更为丰富.在54株菌中都出现了300 bp和1 300 bp两个特异且稳定出现的条带,这两个特异条带可能是产脂肪酶菌株的SCAR标记条带.     

DNA同源性分析最终确定新疆中华根瘤菌（Sinorhizobium xinjiangensis）为一独立种

针对S.xinjiangensis分类地位的争议,从新疆再次分离获得34株快生大豆根瘤菌,在16SrDNAPCR-RFLP分析和SDS全细胞蛋白电泳分群的基础上,进行了16SrDNA全序列相似性和DNA同源性分析.所测4个菌株和S.fredii模式菌株USDA205的16SrDNA全序列有很高的相似性.而DNA同源性分析说明新分离的菌株代表与原定的S.xinjiangensis为一个DNA同源群.其模式菌株CCBAU110与S.fredii的2株参比菌株USDA194、2048之间的DNA同源性分别为31.5%和28.7%.S.fredii的模式菌株USDA205与新分离的菌株代表及原定的S.xinjiangensis的模式菌株和2个参比菌株之间的DNA同源性为20.8%～39%,远低于70%.属于种水平上的差异.按照国际细菌分类委员会以DNA同源性≥70%且△Tm≤5℃作为定种的标准,S.xinjiangensis是Sinorhizobium属中不同于S.fredii的一个独立的种.表3参20     

慢生型大豆根瘤菌的遗传多样性研究

采用选择性扩增片断长度多态性 (简称AFLP)DNA指纹技术对来自泰国北部的 2 45株慢生型大豆根瘤菌进行遗传多样性的研究 .通过AFLP图谱揭示出该地区的慢生型大豆根瘤菌有较显著的遗传多样性 .从 2 45株中选择出 92个代表株用计算机进行的树状图分析结果表明 ,所分析的菌株在 82 %的相似性水平上聚类成 8个群 .对这 92个代表株的部分菌株和慢生型大豆根瘤菌的参比菌株进行多聚酶链反应 (PCR)扩增的 16SrDNA的 4种限制性内切酶长度多态 (简称 16SrDNAPCR RFLP)分析 ,得出 2个不同的 16SrDNAPCR RFLP类型的菌株 ,分别与慢生型大豆根瘤菌的参比菌株Bradyrhizobiumjaponicum和Bradyrhizobiumelkanii相同 .图 1表 2参 14     

Development of a PCR strategy for thraustochytrid identification based on 18S rDNA sequence

The identification and characterization of the thraustochytrids, an emerging economically and biotechnologically important group of marine heterotrophic protists, is usually based on morphological characters. In this research we used molecular markers to identify thraustochytrids. We designed three sets of primers based on the 18S rDNA sequence alignment of known strains and employed a PCR (polymerase chain reaction) strategy to identify unknown thraustochytrid isolates. DNA from 26 thraustochytrids (three isolated from primary cell cultures of the tunicate Botryllus schlosseri and 23 from a coral holding aquarium) were amplified by these primers, revealing 21 isolates with three bands each, which were assigned to two groups according to PCR fragment sizes. Taxonomic characterizations were deduced by comparing with GenBank data. Four isolates were further studied by sequencing their 18S rDNA. Sequence alignments and phylogenetic analysis revealed that isolates from the coral aquarium (7-5 and 8-7) were highly similar to each other and 95.0-97.0% similar to Thraustochytrium multirudimentale and Schizochytrium minutum. Isolates from the tunicate primary cell cultures (BS1 and BS2) were also closely related to each other and 84.3-86.0% similar to labyrinthulid quahog parasite and Thraustochytrium pachydermum. AFLP (amplified fragment-length polymorphism) analysis revealed 2.5-3.6% differences within the genomic DNA of each group, showing that each isolate is different, although isolates within each group may belong to the same species, in spite of differences found in the general morphology.     

Nuclear ITS region of the alga Heterosigma akashiwo (Chromophyta: Raphidophyceae) is identical in isolates from Atlantic and Pacific basins

The internal transcribed spacer (ITS) region from 19 isolates of the algal genus Heterosigma (Chromophyta: Raphidophyceae) was amplified by polymerase chain-reaction (PCR) and sequenced. Isolates were obtained from both the Atlantic and Pacific basins, including Europe, eastern North America, western North America, Japan and New Zealand. This study presents evidence that all Heterosigma isolates in this study are representatives of one species (H. akashiwo). All 19 isolates, except one (LB 2005) had identical ITS sequence (98.31% similar by pairwise comparison); Isolate LB 2005 may represent a separate subspecies. Such high degree of ITS sequence identity implies that the organism has spread between oceanic regions in geologically recent times, possibly by human means. In addition to those from Heterosigma spp., the ITS regions from other marine Raphidophyceae (Chattonella antiqua, C. marina, C. subsalsa, Fibrocapsa japonica, and Olisthodiscus luteus) were amplified and sequenced using PCR. Total ITS lengths differed among the Raphidophyceae (C. antiqua, 577 base pairs (bp); C. marina, 577 bp;. C. subsalsa, 579 bp; F. japonica, 830 bp; H. akashiwo, 561 and 563 bp; O. luteus, 829 bp), but 5.8S rDNA sequences were similar in size (13 to 142 bp). The high ITS sequence identity between C. antiqua and C. marina (>99.9% by pairwise comparison) suggests the need for a taxonomic review of these species encompassing all morphological, genetic, physiological and biochemical information. Additionally, a number of cultures of Raphidophyceae were positively identified. In general, ITS comparisons among the Raphidophyceae may be most useful at the level of species determination rather than at the population level. Received: 12 July 1999 / Accepted: 16 March 2000     

Symbiont diversity within the widespread scleractinian coral<Emphasis Type="Italic"> Plesiastrea versipora</Emphasis>, across the northwestern Pacific

The molecular diversity of symbiotic dinoflagellates associated with the widespread western Pacific coral Plesiastrea versipora was explored in order to examine if associations between reef-building corals and symbiotic dinoflagellates change with environment. Several ribosomal DNA genes with different evolutionary rates were used, including the large subunit (28S), the 5.8S region and the internal transcribed spacers (ITS). The phylogenetic analysis of the 28S and 5.8S rDNA regions indicated that a single endosymbiont species, highly related to one of the species of Symbiodinium in clade C (= Symbiodinium goreaui, Trench et Blank), associates with P. versipora along the Ryukyu Archipelago. The persistence of the same endosymbiont within P. versipora across this wide array of latitudes may be a result of such features as the Kuroshio Current, which brings tropical temperatures as far north as Honshu, Japan. Analysis of the faster evolving ITS rDNA region revealed significant genetic variability within endosymbionts from different populations. This variation was due to a high degree of interpopulation variability, based on the proportion of pairwise variation detected among the populations (0.95% approximately). By comparison with other studies, the results also indicate that some ITS1 haplotypes from P. versipora endosymbionts seem to be widely distributed within the western Pacific Ocean, ranging from the Great Barrier Reef to the northeast of the China Sea.     

ERIC-PCR:一种快速鉴别环境细菌菌株的方法

以 Ｅ Ｒ Ｉ Ｃ（ 肠杆菌基因间共有重多序列） 序列设计的特异引物对３ 株大肠杆菌、３ 株软腐欧氏杆菌、２ 株草生欧氏杆菌、１ 株梨火疫欧氏杆菌、１ 株催娩克氏菌、１ 株阴沟肠杆菌和９ 株具有降酚能力的细菌等２０ 种细菌的基因组 Ｄ Ｎ Ａ 进行 Ｐ Ｃ Ｒ 分析．每种菌株均存在数目不等的各自独特的带型,能够区分同一种类中极为相近的菌株．经多次重复,各特异性扩增的主要带型能重复稳定出现．聚类分析的结果表明,供试菌株多数按照分类地位归到相应的组中．９ 种具有降酚能力的细菌中,２ 种分离自处理焦化废水池活性污泥,７ 种来自土壤样品． Ｅ Ｒ Ｉ Ｃ Ｐ Ｃ Ｒ 指纹图显示,前２ 种属于一类,都有一条大小约１ ．１ ｋｂ 的主带,其它７ 种土壤中分离出来的细菌除其中１ 种有１ 条约１ ．２ ｋｂ 大小的主带外,其余６ 种都有１ 条大小约１ ．４ ｋｂ 的带．聚类分析将从土壤中分离出来的细菌归为３ 种不同的类型． Ｅ Ｒ Ｉ Ｃ Ｐ Ｃ Ｒ 可以从分子水平对细菌基因组进行快速指纹图分析,在对环境细菌分离物进行快速鉴定和归类等方面具有实用价值     

林木外生菌根真菌彩色豆马勃巢式PCR检测

为探讨林木外生菌根真菌的分子检测方法,利用真菌通用引物ITS1-F/ITS4-B扩增了外生菌根真菌彩色豆马勃的核糖体DNA内转录间隔区并进行了序列测定.通过序列比较,设计了一对彩色豆马勃特异性引物PtF/PtR.利用该对特异性引物与ITS1-F/ITS4-B组合进行巢式PCR,能从供试的彩色豆马勃10个菌株中特异性地扩增出1条347 bp的条带,而供试的其他6个参比菌株未出现扩增产物.经分析,该巢式PCR检测技术的灵敏度可达到10 fg的DNA,是常规PCR检测的1 000倍.利用该技术从马尾松苗木菌根中检测到目的外生菌根真菌.这表明采用本研究设计的特异性引物,利用巢式PCR技术可以灵敏、准确地从林木外生菌根中检测出彩色豆马勃.     

基因间隔序列(ITS)在细菌分类鉴定和种群分析中的应用

Use of 16S -23S intergenic transcribed spacer (ITS) variability, as a relatively new method, is becoming an important supplement to the molecular methods based on 16S rRNA for which has a fairly constant size and is not divergent enough to give good separation in close relationships. This paper summarizes the structures and characteristics of ITS regions that are extremely variable in copy number, length and sequence per genome. The ITS region can be amplified easily taking advantage of conserved nucleotide stretches at the 5′of the 16S and 3′of the 23S gene, and the amplicon can contain different amounts of the 16S rDNA by choosing primers at different conserved areas within this gene. These primers are listed and discussed for perfecting the methodology of ITS. Furthermore, some recent progresses on the taxonomy, identification and community analysis of bacteria by means of ITS in epidemiology, ecology and artificial environment are reviewed, as well, the virtues and limitations of that method are discussed. Fig 2, Tab 1, Ref 51     

原废水培养基分离活性污泥中的苯酚降解细菌

用未经处理的含酚焦化工业废水为基础配制培养基，采用平板涂布法，在10^-5稀释度下得到100个单菌落分离物．它们均能在以苯酚(500-800mg L^-1)为唯一碳源的无机盐培养基上生长，其16S rDNA基因的ARDBA多态性分析将这些分离物划分成4个分类操作单元(OTUs)．各单元代表株的16S rRNA基因序列分析和检索结果表明，97个分离物与Alcaligenes faecalis同源性达99％，2个分离物分别与Arthrobacter nicotianae和Klebsiella sp.99％同源．另一个分离物与Ochrobactrum sp．96％同源．苯酚经化酶大亚基基因(LmPHs)PCR扩增表明，除类似Arthrobacter nicotianae的菌株外，其它3个分类操作单元的降酚菌都能利用多组分苯酚经化酶代谢途径进行酚代谢．图2表2参11