Bombyx acid cysteine proteinase

Summary

Three kinds of yolk proteins (vitellin, egg-specific protein and 30 k-proteins) are found in silkmoth eggs and have been well characterized. Essentially these proteins are considered to be amino acid reserves for developing embryos. Since at an early stage of egg development the cysteine proteinase accounts for the majority of the total proteinase activity, it may be involved in the degradation of yolk proteins. The enzyme is stored in the eggs as an inactive pro-form, indicating that the activation of the enzyme might be one of the key steps in yolk protein degradation. To investigate at the molecular level how yolk proteins degradation takes place, we have studied Bombyx acid cysteine proteinase (BCP) during an early period of embryonic development. We summarize how proteinases are regulated and are involved in the degradation of Bombyx yolk proteins during embryogenesis. These will be discussed mainly in light of recent results obtained from eggs of the silkmoth, Bombyx mori.     

基于宏基因组测序技术揭示大泷六线鱼肠道微生物特征北大核心

对大泷六线鱼不同生长期肠道微生物进行分析。【目的】基于宏基因组学技术揭示其肠道微生物变化特征及其与营养的联系。【方法】对大泷六线鱼仔鱼、稚鱼和幼鱼肠道微生物样本进行HiSeq高通量测序,分析菌群结构,比较微生物群落的多样性,探究生长过程中肠道微生物的相互演替及功能关系。【结果】门水平上,鱼肠道微生物在生长过程中优势菌门变形菌门(Proteobacteria)递减,而厚壁菌门(Firmcutes)递增;属水平上,仔鱼期的弧菌属(Vibrio)(37.8%)、稚鱼期的发光杆菌属(Photobacterium)(77.8%)、幼鱼期的乳酸菌属(Lactococcus)(42.5%)占优势,微生物群落组成发生显著变化;且仔鱼期的多样性高,幼鱼期的丰富度高;物种差异也呈现着与生长特征的相关性,幼鱼期差异标志物是厚壁菌门、芽孢杆菌纲(Bacilli)、乳酸杆菌目(Lactobacillales)、链球菌科(Streptococcaceae)、乳球菌属(Lactococcus)和乳酸乳球菌(Lactococcus lactis);稚鱼期差异标志物是发光菌属、托鲁尼发光菌(Photobacterium toruni);仔鱼期差异标志物是Phaeobacter inhibens、Colwellia aestuarii和Colwellia polaris等。宏基因组功能水平分析显示,KEGG数据统计代谢功能占优势,随生长呈现递增趋势,鱼肠道微生物群在碳水化合物代谢、氨基酸代谢、核苷酸代谢、能量代谢,以及辅助因子和维生素代谢中起着重要作用;从蛋白注释功能上也呈现了类似的结果,碳水化合物代谢(3350)和氨基酸代谢(2424)占代谢通路主要组成部分。功能差异分析表明,随着生长变化,微生物功能逐渐适应机体和环境需求,稚鱼期差异主要体现在能量代谢和糖降解功能;仔鱼期差异显著的是细胞的生长、死亡和凋亡功能,主要体现在光合作用方面;幼鱼期主要体现是二级代谢物的生物合成,其次是糖酵解和糖异生等碳水化合物代谢等。【结论】大泷六线鱼仔、稚、幼不同生长期肠道微生物结构存在显著差异,生长发育改变肠道微生物菌群的功能,采用差异物种和差异功能综合判定生长所需的营养,有助于提高养殖效益,为绿色健康生态养殖提供理论基础。     

A Simple Qualitative Representation of Polypeptide Chain Folds: Comparison of Protein Tertiary Structures

Abstract

A new simple quantitative representation of three-dimensional structure of globular proteins is proposed which is useful for comparison of distantly related problems, computer sorting of large sets of conformations, and search of structurally similar domains in protein data base. The folding course of the polypeptide backbone is approximated by a set of successive vectors corresponding to the elements of regular secondary structure (e.g. α-helices, strands of β- sheets) and non-regular segments. The parameters specifying the spatial organization of segments in this vector model are internal coordinates, namely, lengths of the vectors, planar and dihedral angles. Quantitative representation proposed allows to circumvent the problem of insertions/deletions and to avoid the stage of best superposition during protein comparison An application was made to the comparison of three-dimensional structures of scorpion toxins Centruroides sculpturatus Ewing v-3, Buthus eupeus M₉ and I_5A, which have different chain lengths and low sequence similarity.     

牛支原体LRR5蛋白原核表达及其在牛支原体入侵宿主细胞过程中的作用分析

致病性支原体具有入侵宿主细胞的能力,这是其发挥致病作用的关键。介导支原体入侵宿主细胞的自身功能蛋白可能是一种潜在的药物或疫苗靶标。【目的】克隆表达牛支原体(Mycoplasmabovis) MBOVPG45_0564基因编码蛋白(命名为LRR5蛋白),并探究其在M. bovis入侵宿主细胞过程中的作用。【方法】利用NCBI数据库对MBOVPG45_0564基因进行同源性分析,用Discovery Studio Client系统对LRR5蛋白进行蛋白结构预测;原核表达LRR5蛋白并制备其小鼠多克隆抗体,利用免疫电镜对LRR5蛋白进行亚细胞定位;通过平板计数、激光共聚焦显微镜观察LRR5抗体封闭后M. bovis对胎牛肺(embryonic bovine lung, EBL)细胞入侵率的变化;将LRR5蛋白偶联至荧光微球表面后,以激光共聚焦显微镜及高内涵活细胞成像系统观察微球进入EBL细胞情况。【结果】MBOVPG45_0564基因在牛支原体属中为保守基因,其编码蛋白LRR5为膜相关蛋白,空间构象呈典型的月牙状,多个重复的亮氨酸基序以超螺旋方式组装并形成螺线管蛋白质结构单元。LRR5抗体封闭后,M. bovis对EBL细胞的入侵率显著降低(P<0.05),荧光微球偶联LRR5蛋白后,荧光微球可成功进入EBL细胞。【结论】MBOVPG45_0564基因编码的LRR5蛋白定位在M. bovis膜上,在M. bovis入侵宿主细胞过程中发挥着重要作用。     

嗜盐菌群对酸性金黄G的脱色特性和机理

【目的】为了获得能够在高盐环境下脱色偶氮染料的嗜盐菌群及其降解机理。【方法】采用富集驯化的方法获得一个嗜盐菌群,采用Illumina HiSeq2500测序平台对其群落结构进行测定;采用分光光度法测定了其降解特性;采用GC-MS和红外图谱分析了其降解机理;采用微核实验的方法比较了偶氮染料降解前后的毒性。【结果】该菌群在10%的盐度下,使100mg/L的酸性金黄G在8h内脱色。菌群主要由Zobellella、Rheinheimera、Exiguobacterium和Marinobacterium组成。最适宜的脱色条件是:pH=6,酵母粉为碳源,蛋白胨或硝酸钾作为氮源,盐度为1%–10%。酸性金黄G降解产物的毒性比降解前降低。酸性金黄G主要的降解产物是对氨基二苯胺和二苯胺。此外,该菌群还能使酸性大红GR和直接湖蓝5B等多种偶氮染料脱色,具有较好的脱色广谱性。【结论】获得了快速降解偶氮染料的嗜盐菌群及降解机理,为该嗜盐菌群应用于高盐印染废水的处理提供菌种资源和理论支持。     

枯草芽胞杆菌异戊二烯酶ComQ的生物信息学分析及对生物膜形态的影响

[目的]枯草芽胞杆菌ComQ是一种类异戊二烯生物合成酶.利用生物信息学预测分析了ComQ的生物学特性,对comQ基因进行过表达和敲除,构建突变菌,孔板发酵培养验证生物膜形态变化.[方法]运用NCBI (National Center for Biotechnology Information)网站里的Protein数据...     

Coronin7 forms a novel E3 ubiquitin ligase complex to promote the degradation of the anti-proliferative protein Tob

Tob belongs to the anti-proliferative Tob/BTG family. The level of Tob throughout the cell cycle is regulated by the SCF (Skp1/Cullin/F-box protein)^Skp2 ubiquitin ligase (E3) complex. Here, we show that Coronin7 (CRN7) is also involved in Tob degradation. We identified CRN7 as a Tob-interacting molecule. A sequence containing two of the six WD motifs in the middle of CRN7 was responsible for the interaction. CRN7 enhanced the polyubiquitination of Tob in vitro, and overexpression of CRN7 promoted proteasome-dependent degradation of Tob. Furthermore, CRN7 interacted with Cullin1 and Roc1 to form a novel SCF-like E3 complex, suggesting that Tob protein is regulated by multiple ubiquitination machineries.

Structured summary

Cullin1physically interacts with CRN7: shown by anti tag coimmunoprecipitation (view interaction)Roc1physically interacts with CRN7: shown by anti tag coimmunoprecipitation (view interaction)CRN7physically interacts with Tob1: shown by anti tag coimmunoprecipitation (view interaction)CDC34physically interacts with CRN7: shown by anti tag coimmunoprecipitation (view interaction)Tob1 and CRN7colocalize: shown by fluorescence microscopy (view interaction)Elongin Bphysically interacts with CRN7: shown by anti tag coimmunoprecipitation (view interaction)Elongin Cphysically interacts with CRN7: shown by anti tag coimmunoprecipitation (view interaction)Tob1physically interacts with CRN7: shown by two hybrid (view interaction)     

Lindane degradation by root epiphytic bacterium Achromobacter sp. strain A3 from Acorus calamus and characterization of associated proteins

Abstract

Lindane degrading root epiphytic bacteria were isolated from wetland plant Acorus calamus. Bacterial strain A3 identified as Achromobacter sp. A3, showed maximum degradation potential of 88.7?±?1.24% for 50?mg?l^?1 lindane. Lindane biodegradation was followed by decrease in pH as well as increase in concentration of chloride ions in the culture medium. Lindane degradation potential of Achromobacter sp. A3 was also studied at different concentrations of lindane. Maximum degradation was at 10?mg l^?1 followed by 50?mg l^?1 and 100?mg l^?1 lindane. Also, lindane induced proteins were studied using SDS-PAGE. The induced proteins were identified as alpha/beta hydrolase fold-3 domain-containing protein, involved in lindane hydrolysis and extracellular solute-binding family protein having role in transmembrane transport of lindane for utilization of lindane by bacteria. The appearance of unique polypeptides in lane corresponding to media supplemented with lindane showed that the exposure of bacterial cells to lindane has resulted in regulative expression of certain proteins. So far as known, this is the first report to isolate and study lindane degrading root epiphytic bacteria from A. calamus.     

Physiological,biochemical, and fluorescence parameters of senescing sugar beet leaves in the vegetative phase of growth

The phase of vegetative growth of sugar beet (Beta vulgaris L., single-sprout form) was conditionally subdivided into four periods according to leaf number and size (including already withered leaves): (A) 8 ± 1 weeks after seedling emergence (wase) (5–7 leaves); (B) 11 ± 1 wase (10–12 leaves); (C) 14 wase (13–15 leaves); (D) 15 wase (15–18 leaves). It took each next leaf about 1 week to come into view. In the course of leaf senescence, palisade parenchyma became less ordered; cells, vacuoles, and intercellular spaces expanded; leaf area and thickness increased. Chloroplasts became swollen, starch grains (and later osmiophilic globules) accumulated and degraded. In every growth period, the highest levels of soluble carbohydrates (sCH), chlorophyll (Chl (a + b)), soluble protein, and the highest activities of rubisco and soluble carboanhydrase usually preceded the full leaf expansion. In unfolded leaves at the growth period B, the maximum values of biochemical characteristics were as a rule higher than at the growth periods A and C and especially D. The only exception was Chl (a + b) with its peak level somewhat increased with plant age. Occurrence of peak values of individual characteristics depended on plant growth period. These characteristics started diminishing asynchronously, with a minimum in old operational leaves. Only the sCH content in the leaves at the periods C and D was stable. Changes in quantum yield at PSII and nonphotochemical fluorescence quenching reflected the age-associated differences in biochemical characteristics. The results are discussed in the light of the idea that leaf senescence is a normal stage of development directly related to the changes in source-sink relations. Biochemically, this stage comprises the degradation of temporarily stored products and partial utilization of the breakdown products for maintenance of the growth of newly formed leaves and root.     

过表达PDI对毕赤酵母分泌淀粉样蛋白的影响——以胱抑素为例

[目的] 本研究旨在结合酵母菌蛋白质二硫键异构酶（protein disulfide isomerase,PDI）与其底物蛋白鸡胱抑素C （chicken cystatin C,cC）在酵母中的共表达,理解PDI影响外源蛋白合成与表达的调控规律。运用转录组深度测序技术（RNA-Seq）筛选差异基因,调取并鉴定影响cC表达的关键基因,为解析外源蛋白高效表达机制,改造工程菌株提供理论支撑。[方法] 以巴斯德毕赤酵母GS115、GS115-cC为出发菌株,采用电转的方法将携带PDI编码基因的载体pPIC3.5K转入到GS115/GS115-cC菌株,使其在菌株中过表达,研究过表达PDI对cC表达的影响。采用RNA-Seq深度测序方法,研究重组毕赤酵母基因表达差异情况。并结合KEGG注释结果对数据进行分析,挑选差异显著表达基因进行验证,初步明确其在蛋白表达调控方面的功能。[结果] 本研究通过构建过表达PDI重组毕赤酵母菌株,使得外源蛋白cC的表达量显著增加。利用RNA-seq技术分析过表达PDI菌株与正常菌株的差异,最终筛选了373个差异表达基因,其中有122个差异基因注释到KEGG生物通路,包括12个基因注释到蛋白质转运和分解代谢途径,21个基因注释到蛋白质折叠分选和降解途径,以及24个基因参与蛋白质的翻译途径等。[结论] 在毕赤酵母中过表达PDI能显著增加外源蛋白cC的表达量。通过对过表达与正常表达PDI的毕赤酵母基因的表达谱分析,初步确定了其中一些转录情况变化显著的基因,明确了它们参与的细胞途径和信号通路,为改造具有高效率表达淀粉样蛋白的酵母菌株奠定基础。     

院前急救服务地理可及性指标计算与可视化表达研究

?????? 目的 探索院前急救服务地理可及性指标的计算方法及可视化表达的技术。方法 通过分析院前急救服务的特点及影响院前急救服务地理可及性的因素,确定反映院前急救服务地理可及性的指标;应用地理信息系统,确定指标计算与可视化表达的技术,并应用某市数据进行模拟实验,检验方法的可行性与可视化表达的效果。结果 急救中心与急救医院的地理布局、急救中心车辆的配置是影响院前急救服务地理可及性的两大重要因素,分别通过到达急救中心与急救医院的距离、每万人拥有的急救车辆数来评价,两个指标经标化相乘来综合反映居民获得院前急救服务的方便程度;以ArcGIS10.0软件为平台进行指标的具体计算与可视化表达。结论 地图可视化表达院前急救服务地理可及性直观展示了急救资源的地理布局及地理可及性的区域差异。     

一株林可霉素降解菌的筛选鉴定及其降解机制

【背景】抗生素污染越来越引起人们的关注。利用微生物处理抗生素污染被认为是一种环境友好型的方法。【目的】筛选林可霉素高效降解菌并研究其降解机制。【方法】经形态学观察、生理生化鉴定和16S rRNA基因测序分析进行鉴定;通过PCR技术和质谱分析技术对该菌抗性基因和降解产物等进行分析。【结果】从林可霉素菌渣堆肥样本中获得一株高效降解林可霉素的假单胞菌(Pseudomonas RST-1),该菌在林可霉素浓度为3.0 g/L的牛肉膏蛋白胨培养基上培养40 h后,林可霉素降解率高达57.3%。该菌含有intI1、sul1、sul2等抗性基因,降解产物为去甲基林可霉素和2-丙基-N-甲基脯氨酸。【结论】菌株RST-1具有高效降解林可霉素的能力,推测可能的降解机制为去甲基化和酰胺键水解作用,该菌株降解特性及降解机制研究为林可霉素降解工程菌及其高效降解菌剂的研制奠定了基础。     

一株耐碱高效长链烷烃降解菌C24MT1的筛选及其降解特性

【背景】石油被称为“液体黄金”,人类的工业生产活动在利用其创造巨大社会价值的同时,也对自然环境造成了严重的污染。微生物修复技术是现阶段治理石油类污染有效的手段之一,具有经济、高效、无二次污染等优点。【目的】从受石油污染的土壤中分离高效降解长链烷烃正二十四烷的菌株,探究其降解特性及在微生物修复中的应用前景。【方法】通过形态学及16S rRNA基因测序进行菌株鉴定,采用气相色谱法检测菌株对正二十四烷的降解效果,并结合气相色谱-质谱(gas chromatography-mass spectrometer, GC-MS)分析降解中间产物以推测其潜在代谢途径。【结果】筛选到一株可高效降解正二十四烷的菌株C24MT1,经鉴定为不动杆菌属(Acinetobacter)。该菌株最适降解条件为30 °C、pH 9.0、盐度2 g/L,该条件下生长7 d对9 g/L正二十四烷的降解率高达86.63%;与此同时,菌株在强碱性环境(pH 11.0)中生长良好(OD₆₀₀为0.39)并保持较高烷烃降解率(75.38%),对极端环境具备较强的耐受能力;对降解中间产物进行分析,推断菌株代谢长链烷烃正二十四烷的途径可能包括末端氧化及次末端氧化。【结论】不动杆菌C24MT1具有良好的环境适应能力及烷烃降解能力,在后续微生物菌剂开发和石油类污染土壤的环境修复领域具有巨大的应用前景。本研究可为盐碱地区高浓度石油类污染土壤的修复提供优良菌种,并进一步丰富石油烃类生物降解的菌种资源库。     

包埋法固定化对硫氧化微生物菌群结构和功能的影响

【目的】为探讨包埋法固定化过程对硫氧化菌群硫化物去除能力及菌群微生物群落结构的影响,【方法】以聚乙烯醇-海藻酸钠-活性炭为载体,对硫氧化菌群进行了固定化,并采用富含硫化物的无机盐培养基,对比固定化与非固定化硫氧化菌群对硫化物的氧化去除能力。同时,利用PCR-DGGE技术,探讨硫氧化菌群在固定化前后以及在硫化物氧化去除过程中微生物群落结构变化。【结果】在对硫氧化菌群进行固定化之后,12 h之内对硫化物的最大去除能力从1000 mg/L下降为600 mg/L。硫氧化菌群的微生物群落结构发生了明显变化,但菌群中的硫氧化菌Catenococcus thiocycli未受影响,硫氧化菌Thioclava pacifica在菌群中的地位反而得到了强化。【结论】受制于底物在载体材料中的扩散迁移效率,硫氧化菌群对硫化物的氧化去除能力在固定化之后有所下降。由于不同微生物对固定化形成的微环境的适应能力以及对载体附着能力的不同,固定化对硫氧化菌群的微生物群落结构产生较大影响。     

青藏高原高寒草甸退化对矮嵩草有关生理特性的影响

该研究采用空间分布代替时间演替的方法,选取青藏高原青海省果洛藏族自治州玛沁县境内典型的未退化草甸和退化草甸样地,分别设置3个5m×5m的样方,于6至9月下旬上午进行植株和土壤采样,测定矮嵩草生理指标,探讨高寒草甸退化所导致的环境变化对自然生长状态下矮嵩草生理特性的影响机制。结果表明:(1)与未退化草甸相比,退化导致土壤表层速效氮含量极显著降低,而速效磷和速效钾含量显著升高;全氮、全磷和全钾的含量总体上表现为未退化草甸低于退化草甸。(2)与未退化草甸相比,退化草甸矮嵩草叶中超氧化物歧化酶(SOD)活性在生长前期高而后期低(低4%),谷胱甘肽(GSH)含量在两个样地的变化趋势基本一致。(3)退化草甸矮嵩草叶片可溶糖和可溶蛋白含量在生长后期分别比未退化草甸降低17.6%和34.9%,且9月份降低达极显著水平。(4)生长中期以后,退化草甸矮嵩草叶片叶绿素a、b含量比未退化草甸的下降速度快、含量分别低18.84%和20.68%。(5)退化草甸矮嵩草叶片超氧阴离子自由基(O_2~)的产生速率在9月份极显著高于未退化草甸。研究表明,在非生物胁迫下未退化草甸的矮嵩草具有更高的ROS清除能力和渗透调节能力,退化导致的环境变化可能是矮嵩草在生长后期抗氧化能力降低、衰老早的内在原因。     

黄翅大白蚁后肠优势菌大白蚁营发酵菌的全基因组序列分析

【目的】营发酵单胞菌属Dysgonomonas是黄翅大白蚁后肠的第二优势微生物。前期研究中,我们从黄翅大白蚁后肠分离出一种命名为大白蚁营发酵菌的新菌。为深入了解大白蚁营发酵菌在宿主白蚁体内发挥的作用和功能,有必要解析大白蚁营发酵菌的基因组序列信息。【方法】使用Illumina Miseq测序平台获取该菌的全基因组序列,将其全基因组序列经过注释的基因蛋白质序列提交COG和KEGG数据库进行BLASTp比对分析,确定该菌潜在的重要酶类和代谢途径,并对个别纤维素酶活进行检测。【结果】大白蚁营发酵菌整个基因组大小为4655756 bp,GC含量为38.54%,DDBJ数据库登录号为BBXL01000001–BBXL01000078。生物信息学分析结果表明菌株大白蚁营发酵菌具有多个木质纤维素降解酶基因,且具备完整的木质纤维素降解和乙酸、乳酸生成通路。此外发现该菌株中存在与氮源代谢和抵御病原体相关的基因。【结论】本研究首次解析大白蚁营发酵菌的全基因组序列,了解其基因组基本特征,初步探讨了该菌降解木质纤维素的过程,为细菌协助宿主白蚁降解木质纤维素提供了理论基础,同时为该菌可能参与宿主白蚁氮源代谢和抵御病原体入侵提供了依据。     

生物竞争抑制作用对渤海J油田微生物降解驱油聚合物功能的影响

【目的】揭示可降解驱油用聚合物的油藏内源微生物群落组成,分析生物竞争抑制作用(bio-competitive exclusion,BCX)对微生物聚合物降解功能的影响。【方法】通过室内培养实验,观察BCX对驱油用聚合物黏度的影响,随后借助高通量测序技术分析渤海J油田中与聚合物降解相关的微生物菌种,并探寻样本中丰度较高的聚合物降解功能基因─酰胺酶、加氧酶、硫化氢生成酶基因。之后,比对测序结果,采用实时荧光定量法验证上述功能基因在样本之间的含量差异,最后进一步注释携带上述功能基因的微生物群落组成。【结果】BCX可有效地延缓驱油聚合物黏度的损失。油田中与聚合物降解相关的微生物有Acetomicrobium、 Tepidiphilus、Thermoanaerobacter、Fervidobacterium、Ralstonia、Halomonas、Roseovarius、Deferribacteraceae和Comamonadaceae等9类菌种。高通量测序分析得到样本中BCX可显著下调丰度的聚合物降解功能基因共计有7种,其中酰胺酶基因ansB、加氧酶基因ssuD在样本之间的含量经定量验证,发现...     

微泡菌属菌株YPW1和YPW16多糖降解特性分析

【背景】海洋环境中分离到的微泡菌属菌株具有多糖降解能力,在环境中可以作为糖类代谢的重要执行者参与海洋碳循环过程。【目的】测定2株微泡菌属菌株的多糖降解活性,通过与微泡菌属其他菌株基因组比较分析2株菌的多糖降解基因特征。【方法】通过3,5-dinitrosalicylicacid(DNS)定糖法测定多糖降解活性,同时利用高通量测序技术对菌株基因组序列进行测定与组装,并与其他基因组注释结果进行比较分析。【结果】分离得到2株微泡菌属菌株YPW1和YPW16,二者均为潜在新种。结果表明,菌株YPW1能够降解琼胶、褐藻胶、果胶、几丁质、木聚糖、淀粉、普鲁兰等7种多糖,而菌株YPW16仅可降解淀粉和普鲁兰。基因组分析表明,YPW1具有上述7种多糖的降解酶基因,但菌株YPW16只具有淀粉酶与普鲁兰酶降解基因。相较于其他微泡菌属菌株,菌株YPW1多糖降解范围、多糖降解酶基因种类与丰度较高,但菌株YPW16多糖降解范围却较为狭窄。由此可知,多糖降解酶基因在微泡菌属基因组中的分布差异性较大。【结论】本研究为微泡菌属提供了2株潜在的新型菌株资源,为生物多糖降解提供了生化工具,也为研究微泡菌属菌株中多糖降解基...     

巴里坤盐湖退化区土壤微生物群落结构及生态功能分析

【目的】微生物是湖泊生态系统的重要组成部分,参与碳、氮和硫等元素的生物地球化学循环过程,其群落组成和功能对环境的稳定性和可持续性至关重要。然而,新疆的部分湖泊出现退化和盐渍化等问题,微生物如何响应湖泊退化值得研究。【方法】本研究基于16S rRNA基因的扩增子高通量测序,对巴里坤盐湖退化区域的土壤微生物群落结构进行分析,同时对微生物的潜在生态学功能进行预测。【结果】本研究发现,假单胞菌门(Pseudomonadota)、绿弯菌门(Chloroflexota)和拟杆菌门(Bacteroidota)是巴里坤盐湖退化生境中的优势类群。在轻度退化阶段,脱硫菌门(Desulfobacterota)和弯曲杆菌门(Campylobacterota)是主要类群,但随着湖泊退化程度加剧,这些类群急剧减少甚至消失;在极度退化阶段,酸杆菌门(Acidobacteriota)和浮霉菌门(Planctomycetota)等类群逐渐占据主导地位。基于BugBase对氧的需求进行预测,结果发现好氧类群主要是放线菌门(Actinomycetota)、假单胞菌门(Pseudomonadota)和绿弯菌门(Chlorof...     

Development and comparison of ELISA and PCR methods for the early detection of Ganoderma disease of coconut

Abstract

Molecular diagnosis, chemo-diagnosis and physiological parameter have been applied for detecting the Ganoderma disease of coconut. Polyclonal antibodies (PAbs) raised against mycelial protein of Ganoderma, specific mycelial protein (62 kDa) of Ganoderma isolates and basidiocarp protein of Ganoderma were used for detection. All the PAbs could detect Ganoderma in diseased coconut root tissues in early stage of the disease before symptom expression by indirect – ELISA at the antiserum dilution of 1:1000 for mycelial protein, 1:700 for specific protein and 1:3000 for basidiocarp protein. Low cross reactions were observed with saprophytic fungi occurring in coconut roots and also with other basidiomycetous fungi. For polymerase chain reaction tests, the primer was generated from the internal transcribed spacer region one (ITS 1) of rDNA of Ganoderma, which produced a PCR product of 167 bp in size. Utility of this method was confirmed at the field level.