南海硇洲岛潮汐带栉江珧可培养细菌的系统发育多样性

【目的】研究南海硇洲岛潮汐带栉江珧(Atrina pectinata)样品相关可培养细菌的多样性。【方法】采用纯培养法和基于16S r RNA基因序列的系统发育分析,法对样品中可培养细菌(含放线菌)的类群多样性、物种多样性和遗传多样性进行研究。【结果】用补充0–25%(质量体积比)Na Cl的MA、MH和NA培养基从栉江珧样品中分离到125株细菌。在形态观察和部分生理生化实验结果的基础上去冗余,选取90个代表性菌株进行基于16S r RNA基因序列的系统发育多样性分析。结果表明,这90个分离菌株分属于3个大的系统发育类群(Gamma-proteobacteria、Firmicutes、Actinobacteria)、6个科、10个属,可分为33个物种。优势类群为厚壁菌门(Firmicutes)(56株,62.2%)和γ-变形杆菌亚门(Gamma-proteobacteria)(31株,34.5%)。大多数菌株与其系统发育关系最密切的已知物种的典型菌株之间存在一定的遗传差异(16S r RNA基因序列相似性为95.7%–99.9%),其中有5株可能代表新的分类单元(Potential new taxa)。分析表明,菌株JSM 112024可能代表了盐单胞菌科(Halomonadaceae)的一个属一级新分类单元;菌株JSM 112019、JSM 114045、JSM 114058和JSM 114083可能分别代表盐弧菌属(Salinivibrio)、芽孢杆菌属(Bacillus)、盐单胞菌属(Halomonas)和枝芽孢菌属(Virgibacillus)的新物种。【结论】湛江硇洲岛潮汐带栉江珧中存在较为丰富的可培养细菌物种多样性和系统发育多样性,并潜藏着较多的新微生物类群(物种)。     

小溪自然保护区非盐环境土壤中嗜盐和耐盐菌多样性

【目的】研究湖南小溪国家级自然保护区普通非盐环境(ordinary non-saline environment)土壤样品中可培养嗜盐及耐盐细菌(含放线菌)多样性。【方法】采用纯培养法和基于16S rRNA基因序列的系统发育分析对样品中嗜盐及耐盐细菌多样性进行研究。【结果】用补充5%-20%(w/v)NaCl的MA、ISP2、ISP5、NA和HAA培养基从土壤样品中分离到114株细菌,其中8株为中度嗜盐菌,19株为轻度嗜盐菌,87株为耐盐菌。根据形态观察和部分生理生化实验结果去冗余,选取61个代表性菌株进行基于16S rRNA基因序列的系统发育多样性分析。结果表明,这些菌株属于细菌域(Bacteria)的3个大的系统发育类群(门;phylum)(Actinobacteria,Firmicutes,Proteobacteria)的16个科、18个属,代表了41个物种。多数菌株属于Firmicutes门(38株,62.3%)和Actinobacteria门(18株,29.5%)。大多数菌株与其系统发育关系最密切的已知物种的典型菌株之间存在一定的遗传差异(16S rRNA基因序列相似性为96.9%-99.8%),其中有7个菌株(JSM070026,JSM081004,JSM081006,JSM081008,JSM083058,JSM083085,JSM084035)代表7个潜在新种(potential novel species)。【结论】研究结果表明,湖南小溪国家级自然保护区普通非盐环境土壤中存在较为丰富的可培养嗜盐及耐盐细菌多样性,并且潜藏着较多新的微生物类群(物种)。     

湛江硇洲岛海葵相关可培养细菌系统发育多样性

【目的】了解湛江硇洲岛海葵样品中相关可培养细菌的多样性。【方法】运用纯培养法和基于16S rRNA基因序列的系统发育分析对样品中可培养细菌多样性进行研究。【结果】用补充0～2.0 mol/L NaCl 的MA、ISP 2、NA、SWA和HAA培养基从海葵样品中分离到126株细菌,通过形态观察和部分生理生化实验去冗余,选取42株具有代表性的菌株进行基于16S rRNA基因序列的系统发育多样性分析。结果表明,42个分离菌株可分为25个物种,属于3个大的系统发育类群(Firmicutes,Gamma-Proteobacteria,Actinobacteria)、11个科、18个属。多数菌株属于Firmicutes门（17株,40.5％）和Gamma-Proteobacteria亚门（14株,33.3％）。这些分离菌株中,至少有6个菌株可能代表6个不同属的6个新物种：JSM 071004、JSM 071068、JSM 071073、JSM 072002、JSM 073008和JSM073097分别代表Bacillus、Halobacillus、Piscibacillus、Pontibacillus、Alteromonas和Nocardiopsis属的新物种。【结论】从以上结果可以看出,湛江硇洲岛海葵中存在较为丰富的微生物物种多样性和系统发育多样性,并且潜藏着较多的新的微生物类群（物种）。     

甜果螨全线粒体基因组测序与分析

【目的】测定和分析甜果螨Carpoglyphus lactis线粒体基因组全序列,并在线粒体基因组水平探讨其在真螨总目(Acariformes)中的系统发育地位,为真螨总目分类及果螨科线粒体基因组研究提供科学依据。【方法】挑取实验室饲养的甜果螨成螨,用传统的酚氯仿抽提法和试剂盒提取法提取甜果螨基因组DNA。然后采用节肢动物或螨类线粒体基因的通用引物PCR扩增出甜果螨线粒体基因cox1,cob,rrnS和nad4-nad5的部分序列;再设计种特异性引物进行Long-PCR扩增和步移法测序,测出甜果螨线粒体基因组全序列。应用SeqMan, SEQUIN 9.0和tRNAscan等生物信息学软件,对甜果螨线粒体基因组的基因结构等进行生物信息学分析。最后基于17种真螨总目螨类的蛋白质编码基因,采用最大似然法构建系统发育树。【结果】甜果螨线粒体全基因组总长为14 060 bp(GenBank登录号:MN073839),为典型的闭合双链DNA分子,共由37个基因组成,包括13个蛋白质编码基因(PCGs)、22个tRNA基因和2个rRNA基因;甜果螨线粒体基因组还包括1个大的非编码区(large non-coding region, LNR)。系统发育分析结果显示,甜果螨Carpoglyphus lactis属于无气门亚目粉螨总科(Acaroidae),与椭圆食粉螨Aleuroglyphus ovatus构成一支。粉螨总科(Acaroidae)和薄口螨总科(Histiostomatoidae)聚成一簇,与痒螨股(Psoroptidia)构成姐妹群。【结论】本研究首次获得并分析了甜果螨线粒体基因组全序列。甜果螨与椭圆食粉螨的亲缘关系较近。     

利用木质纤维素类生物质产微生物絮凝剂Pseudomonas boreopolis GO2的全基因组测序及比较基因组学分析

【目的】Pseudomonas boreopolis GO2可以利用木质纤维素类生物质为唯一碳源发酵产微生物絮凝剂。解析菌株GO2的全基因组特征可为利用木质纤维素类生物质定向合成多糖型微生物絮凝剂提供分子基础。【方法】利用Illumina NovaSeq测序平台对菌株GO2进行测序,用SMRT等软件进行基因组组装、系统发育分析、基因预测和功能注释,并与4株近缘模式株进行了比较基因组分析。【结果】菌株GO2基因组大小为4 498 896 bp,GC含量为69.5%,共编码3 906个基因。菌株GO2与Pseudomonas boreopolis JCM 13306的16S r RNA基因相似性、平均核苷酸一致性(average nucleotide identity, ANI)、DNA-DNA杂交(DNA-DNA hybridization, DDH)值最高,分别为99.93%、98.36%和88.00%,将菌株GO2命名为Pseudomonas boreopolis GO2。比较基因组分析发现,GO2与4个近缘模式菌株共有2 348个直系同源核心基因,主要参与碳水化合物代谢、氨基酸代谢...     

日化产品中洋葱伯克霍尔德氏菌复合群(Bcc)的分类和神秘伯克霍尔德氏菌的耐药性研究

【目的】对从2020–2022年不同日化产品中分离的29株洋葱伯克霍尔德氏菌复合群(Burkholderia cepacia complex,Bcc)进行分类和分型,另将2020年前来源于日化产品中6株被鉴定为Burkholderia lata的菌株进行分类更正。探究神秘伯克霍尔德氏菌(Burkholderia aenigmatica)的耐药性。【方法】本文主要应用多位点分型研究方法(multilocus sequence typing,MLST),PCR扩增atpD、gltB、gyrB、recA、lepA、phaC和trp B 7个管家基因片段,将测序结果与MLST数据库中的数据比对分析,获得菌株各管家基因的编号和ST型(sequence type),对本检测中心分离自日化产品的Bcc进行分型;利用多位点序列分析(multilocus sequence analysis,MLSA),结合MLST中等位基因的核苷酸序列构建进化树,从而对Bcc进行系统发育分析和鉴定。利用最小抑菌浓度法(minimum inhibitory concentration,MIC)测定Bcc对常见防腐剂(1,...     

小溪自然保护区嗜盐及耐盐菌抗菌活性筛选及生物学特征

以8个敏感菌株(3株革兰阳性菌、3株革兰阴性菌和2株真菌)作为指示菌,采用管碟法对分离自湖南小溪自然保护区普通非盐环境(ordinary non-saline environment)土样中的114株嗜盐及耐盐细菌(含放线菌)进行抗菌活性筛选,并对抗菌活性较强的菌株进行了基于16S rRNA基因序列的系统发育分析和生物学特性研究。结果显示,74株受试菌株的发酵产物具有抗菌活性,阳性率为64.9%。综合分析形态特征、生理生化特征和基于16S rRNA基因序列的系统发育分析数据,表明9株具有较强抗菌活性的菌株分别属于Bacillus属(JSM 081049、JSM 082021-1、JSM 082056、JSM 082080、JSM 082081-1、JSM 082097)、Arthrobacter属(JSM082018)、Brachybacterium属(JSM082044)和Streptomyces属(JSM082030)。     

松嫩平原盐碱地中耐(嗜)盐菌的生物多样性

【目的】分离纯化松嫩平原盐碱地中可培养的耐盐菌和嗜盐菌,并分析其生物多样性。【方法】采用纯培养法和定向富集法从该地区盐碱土样中分离耐盐菌和嗜盐菌,然后通过16S rRNA基因同源性比对鉴定所分离细菌的系统发育学地位,从而获取松嫩平原盐碱地中耐盐菌和嗜盐菌的多样性信息。【结果】共分离到细菌40株,分属于细菌域中3个门(Actinobacteria,Firmicutes,γ-Proteobacteria)、8个科、16个属、34个种。其中多数菌株属于厚壁菌门(Firmicutes),最优势属为葡球菌属(Staphylococcus)(8株,占总菌株的20%),其次依次为盐单胞菌属(Halomonas)(5株,12.5%)、芽胞杆菌属(Bacillus)(4株,10%)、大洋芽胞杆菌属(Oceanbacillus)(4株,10%)、库克菌属(Kocuria)(4株,10%)和假单胞菌属(Pseudomonas)(3株,7.5%)等。其中9株细菌的16S rRNA基因序列与最近缘种的同源性在97.2%-99.0%之间,可能为新种。菌株耐盐能力主要在5%-10%之间,其中62.5%的菌株为耐盐菌,其余则为中度嗜盐菌。所有菌株的耐碱能力在pH 9-12之间,其中60%的菌株耐碱能力则高达pH 12,除两株为嗜碱菌,其余均为耐碱菌。【结论】研究结果表明,松嫩平原盐碱地中耐盐菌与嗜盐菌种群丰富,主要以葡萄球菌和盐单胞菌为主,菌株不仅耐盐能力高而且耐碱能力也高,并且该地区可能含有丰富的耐盐菌和嗜盐菌的新物种。     

硇洲岛牡蛎相关细菌抗菌筛选及系统发育分析

以8个敏感菌株作为指示菌,采用管碟法对分离自湛江硇洲岛（20°52′N～20°56′N,110°33′E～110°38′E）潮汐带香港巨牡蛎(Crassostrea hongkongensis)中的72株细菌的发酵液进行抗菌筛选,并对阳性菌株进行基因组DNA提取、16S rRNA基因PCR扩增和序列测定,继而进行系统发育分析。抗菌实验结果表明,受试菌株中有23株菌的发酵产物具有抗菌活性（阳性率31.9%）,其中有5个菌株（JSM 111024、JSM 111027、JSM 111029、JSM 111076、JSM 111083）具有较强的抗菌活性。基于16S rRNA基因序列的系统发育分析表明,这23株菌具有较高的类群多样性和物种多样性,属于3个系统发育群/门(Alpha Proteobacteria、Gamma Proteobacteria、Bacteroidetes)中的8个科(Aeromonadaceae、Flavobacteriaceae、Halomonadaceae、Idiomarinaceae、Phyllobacteriaceae、Pseudoalteromonadaceae、Shewanellaceae、Xanthomonadaceae)的8个属(Idiomarina、Halomonas、Myroides、Nitratireductor、Oceanimonas、Pseudoalteromonas、Shewanella、Wohlfahrtiimonas),可分为11个物种。优势类群为Gamma Proteobacteria亚门（14株）,其中优势属为Oceanimonas属（6株）;第二大类群为Bacteroidetes门（7株）,都属于Flavobacteriaceae科的Myroides属。具有较强抗菌活性的5个菌株中,有4个菌株（JSM 111024、JSM 111027、JSM 111029、JSM 111083）属于Alpha Proteobacteria 亚门Phyllobacteriaceae科〖WTBX〗Oceanimonas属,而菌株JSM 111076属于Gamma Proteobacteria 亚门Aeromonadaceae科Nitratireductor属。     

枯草芽孢杆菌N2-10的基因组测序和比较基因组分析

【背景】枯草芽孢杆菌N2-10是一株具有较强抑菌能力且能产纤维素酶等多种水解酶的革兰氏阳性菌,在发酵饲料中具有较大的应用潜力。【目的】通过获得枯草芽孢杆菌N2-10的全基因组序列信息,进一步解析菌株次级代谢产物合成基因信息,并通过比较基因组学分析菌株N2-10与模式菌株的差异性,为阐明N2-10抑菌和益生机制提供理论基础。【方法】通过二代Illumina NovaSeq联合三代PacBio Sequel测序平台,对菌株N2-10进行全基因组测序,将测序数据进行基因组组装、基因预测与功能注释,并利用比较基因组学分析N2-10与其他菌株的差异。【结果】菌株N2-10基因组大小为4 036 899 bp,GC含量为43.88%;共编码4 163个编码基因,所有编码基因总长度为3594369bp,编码区总长度占基因组总长度的89.04%;含有85个tRNA、10个5S rRNA、10个16S rRNA、10个23S rRNA,以及2个CRISPR-Cas、1个前噬菌体和6个基因岛;在GO (gene ontolog)、COG (clusters of orthologous groups of...     

Phylogenetic analysis ofUlmaceae

A phylogenetic analysis of theUlmaceae, Cannabaceae, Barbeyaceae, andBroussonetia of theMoraceae produced nine equally parsimonious trees with 127 steps. TheUlmoideae (Ulmaceae, sensuGrudzinskaya) are a monophyletic group and distinct from theCeltidoideae. The genusAmpelocera occupies an isolated taxonomic position among the celtidoids. The similarity ofAmpelocera to the fossil celtidoid flowerEoceltis of North America suggests thatAmpelocera posesses an archaic suite of characters, and occupies a primitive position among the celtidoids, theCannabaceae and theMoraceae. The relationships among the other celtidoid taxa,Cannabaceae, andBroussonetia are problematic. TheCannabaceae andBroussonetia of theMoraceae are nested within the celtidoids suggesting that this is a paraphyletic group. The close, but unresolved, relationship of the celtidoids to theMoraceae andCannabaceae observed in this analysis, and the appearance of the celtidoids in the fossil record prior to the ulmoids suggests that the evolutionary relationship of the ulmoids and celtidoids may be more distant than current taxonomic treatments reflect.     

Weighted regression analysis for comparing varietal adaptation

Summary The normally used joint linear regression analysis (OLS) is not appropriate for comparing estimates of stability parameters of varieties when the error variances of site means are heterogeneous. Weighted regression analysis (WLS), in these situations, yields more precise estimates of stability parameters. A comparison of the two analytical methods using the grain yield (kg ha^–1) data of 12 varieties and one hybrid of pearl millet [Pennisetum typhoides (Burm.) S. & H.], tested at 26 sites in India, revealed that the weighted regression analysis yields more efficient estimates of regression coefficients (b _i ) than the ordinary regression analysis, and that the standard errors of b _i values were reduced by up to 43%. The estimated b _i differed with the two procedures. The number of varieties with b _i ssignificantly deviating from unity was not only more (five varieties) with weighted regression analysis than the ordinary regression analysis (one variety), but the classification of varieties as possessing general or specific adaptation differed with the two procedures.     

铁线莲属21个类群的染色体核型分析

铁线莲属(Clematis L.)为毛茛科大属之一,具有重要的园艺与药用价值。为探讨铁线莲属植物染色体组演化规律,揭示属下组间及种间的亲缘关系,该研究采用常规压片法对铁线莲属21个类群的根尖进行处理、压片,对染色体的形态特征进行观察及核型分析,同时利用Ward联接法进行聚类分析研究。狭裂太行铁线莲、毛果扬子铁线莲、卷萼铁线莲、中印铁线莲、钝萼铁线莲的染色体形态为首次报道。结果表明:铁线莲属21个类群均为二倍体,染色体数均为16(2n=2x=16),除中印铁线莲外其他类群均具随体;长瓣铁线莲、钝萼铁线莲、芹叶铁线莲、褐毛铁线莲、C.flammula、毛果扬子铁线莲的染色体为“2B”型,其他类群染色体为“2A”型;铁线莲属核型不对称系数在60.29%~63.79%之间;铁线莲属植物染色体组表现的较为原始,种间核型存在广泛变异。综上结果表明,铁线莲属植物染色体数目应由二倍体向多倍体演化后通过多倍体的二倍化过程产生非整倍体方向演化。铁线莲属染色体的演化主要在二倍体水平上进行,通过产生染色体结构变异的方式实现,通过产生杂合染色体、加强核型不对称性、染色体类型改变以及随体染色体的变化四种途径进化。同时,核型特征在分组水平与物种水平上的划分与传统分类基本一致,说明核型分析可为铁线莲属下组一级分类提供一定的线索。该研究结果为铁线莲属植物系统分类、遗传演化与资源利用等研究领域提供了新的参考资料。     

Phylogenetic analysis of Remipedia (Crustacea)

We present a cladistic analysis of the crustacean class Remipedia, including all 17 extant species currently assigned to the order Nectiopoda, with the Carboniferous fossil Tesnusocaris serving as an outgroup. We applied different methodological approaches and coding options to a basic matrix composed of 26 morphological characters. Our analyses strongly support monophyly of the Godzilliidae and affirm justification of the family Micropacteridae. However, the present taxonomic structure within the Speleonectidae is partly incompatible with our results, and we cannot exclude that the family is paraphyletic.     

Principal components analysis and trend surface analysis of a small-scale pattern in a transition mire

Principal components analysis and trend surface analysis have been applied to a transition mire with the aim to characterize the vegetation pattern and reveal the major trends of variation. The first three PCA axes were ecologically interpretable, viz. the 1 st and 2nd as a complex soil moisture gradient and the 3rd axis as a gradient in the amount of peat in the soil. The ecological interpretability of the 1st axis of PCA after VARIMAX rotation, is unclear because some outlier samples caused a reorientation of the axis. TSA appeared to be useful for the clarification of joint patterns of species groups, which were major contributors to ordination axes in terms of component loadings. The smooth effect of TSA was briefly discussed in connection with the influence of extremes upon the outcoming trend structure. The use of four-variable TSA including a time series is emphasized for the study of spatial-temporal relations and ecological succession.     

Genetic analysis of Aspergillus nidulans AmdS+ transformants

Summary To correlate the genetic background of the Aspergillus nidulans amdS deletion strain MH1277 with the integrational behaviour of transforming vectors, classical genetic methods were used to construct AmdS^- strains in which whole chromosomes had been exchanged with those of a master strain. Progeny strains were transformed to the AmdS⁺ phenotype with vector p3SR2. From Southern analysis it was concluded that transformants from all constructions contained tandemly repeated, multiple copy inserts of vector DNA as found for MH1277-derived AmdS⁺ transformants.AmdS⁺ transformants of MH1277 were analysed genetically to prove that the transformant phenotype is genome linked and that transformation by integration can take place on various chromosomes. In one case the AmdS⁺ property showed linkage to both chromosomes II and IV, due to a chromosomal translocation. Sexual analysis of two transformants with AmdS⁺ insertions on the same chromosome revealed a considerable instability of the AmdS⁺ phenotype in one of the strains upon selfing. Due to this instability no decisive answer could be given for the degree of linkage between the AmdS⁺ insertions in these transformants.     

Restriction pattern analysis of genomic DNA ofFrankia isolates

Summary Total genomic DNAs ofFrankia isolates were subjected to restriction enzyme digestion and subsequent agarose gel electrophoresis. Restriction fragment banding patterns were unique for each isolate and may therefore be used as a method to distinguish between isolates which may be morphologically indistinguishable. This method might be useful for practical purposes such as tracing specificFrankia strains during field studies.     

三叶木通光敏色素A基因的序列及表达分析

光敏色素( phytochrome,简称PHY)是植物体内最重要的光受体,参与调节植物种子萌发、幼苗生长、茎的伸长、子叶伸展直至开花控制等许多生理过程。该研究通过RT-PCR方法首次从三叶木通( Akebia trifoli-ata)中获得了编码光敏色素A的cDNA序列(命名为AktrPHYA1,GenBank登录号为KP864055)。结果表明：该序列由3496 bp组成,包含一个3426 bp的完整开放阅读框,编码1141个氨基酸。 AktrPHYA1编码的蛋白N端为光感受区域,包括一个GAF结构域、一个PHY结构域;C端为光调节区域,C端包括两个PAS结构域、一个组氨酸激酶A结构域和一个类似组氨酸激酶的ATP 激酶结构。同源蛋白比对显示,AktrPHYA1与耧斗菜、荷花的同源蛋白序列一致性分别为83％和82％。遗传进化树分析表明,单子叶植物和双子叶植物的光敏色素A基因分别聚为两支;在双子叶植物中,AktrPHYA1与耧斗菜、荷花PHYA聚在一起,说明三叶木通与耧斗菜、荷花遗传关系较近。 AktrPHYA1在三叶木通茎、叶片、雄花、雌花、种子中均有表达,且在种子中表达最强,在叶片中表达量最低。 AktrPHYA1的组织表达谱暗示了其在植物中可能的功能。该研究结果为三叶木通光敏色素A基因的功能研究奠定了基础。     

Genetical analysis of components of overall plant shape

Summary The genetical control of six characters, which were taken as jointly reflecting the overall shape of the plant, was analysed using four true-breeding lines of Nicotiana rustica. F₁ F₂ and first backcross generations were raised from all of the possible pairwise combinations between the lines. The particular relationships between the lines provided a basis for the analysis which was an extension of the normal model fitting procedures described by Mather and Jinks (1971).The first step in the analysis was to test whether the allelic differences present between the inbred lines p₁ and P₅ had been maintained in the two lines B₂ and B₃₅, derived from an earlier cross between the former. If the allelic differences between p₁ and P₅ were present between B₂ and B₃₅, it was possible to proceed straight-forwardly by fitting a model consisting of m, two symmetrical [d]'s and the relevant non-additive parameters. If B₂ and B₃₅ were homozygous for the same alleles at loci by which p₁ and P₅ differed, in other words if significant asymmetry in the gene distributions was present, the model had to be extended to cover the effects of such genes.All six characters investigated were shown to be subject to genetical variation. From the composition of the genetical models that were necessary to account for the observations from each of the characters, it was inferred that they should be amenable to at least partially independent adjustment by selection.     

滇龙胆GrHDR基因的克隆与表达分析

龙胆苦苷(gentiopicroside)是中药龙胆中的主要药效成分,属于萜类化合物的衍生物。1-羟基-2-甲基-2-(E)-丁烯基-4-二磷酸还原酶[1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate reductase,HDR]是萜类物质合成途径中的关键酶。为探讨不同光照条件下滇龙胆HDR(GrHDR)基因的表达与龙胆苦苷含量之间的关系,该文以滇龙胆叶片cDNA为模板,采用PCR和TA克隆技术获得GrHDR基因序列,对该序列进行生物信息学分析和表达分析,并采用高效液相色谱法测定龙胆苦苷含量,对该基因表达与龙胆苦苷含量进行比较。结果表明:(1)GrHDR基因(GenBank登录号: KJ917165.1)全长1 398 bp,编码465个氨基酸,推定GrHDR蛋白是亲水且稳定的,相对分子质量是52 281.25 Da,理论等电点是5.32;(2)该蛋白属于LYTB蛋白家族,可能定位于叶绿体上,无信号肽,二级结构主要由α-螺旋(45.16%)、β-转角(6.24%)、无规卷曲(33.98%)、延伸链(14.62%)构成;(3)GrHDR蛋白序列与同属植物秦艽的HDR蛋白相似性最高(95.71%);(4)实时荧光定量PCR结果显示GrHDR基因在滇龙胆中的表达量为根 > 叶 > 茎,而在10%、30%、100%全光光照条件下各组织的表达量有很大差异;(5)高效液相色谱法结果显示,不同光照条件下龙胆苦苷含量一致,均为根 > 叶 > 茎,其中100%全光光照下,药用部位根中龙胆苦苷含量达到7.141%,约是30%、10%全光光照条件的两倍,但该结果与同一光照条件下GrHDR基因表达规律不完全一致。该研究为阐述HDR基因功能及其与龙胆苦苷含量的关系提供参考。