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The diversity of gas vesicle genes in Planktothrix rubescens from Lake Zürich

机译:来自苏黎世湖普利克里克斯·鲁西斯卷的燃气囊泡基因的多样性

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Part of the gas vesicle gene cluster was amplified by PCR from three strains of Planktothrix rubescens isolated from Lake Zürich, Switzerland. Each contains multiple alternating copies of gvpA and gvpC. All of the gvpA sequences in the different strains are identical. There are two types of gvpC: gvpC20, of length 516?bp, encodes a 20?kDa protein of 172 amino acid residues (whose N-terminal amino acid sequence is homologous with the sequence of GvpC in Planktothrix [Oscillatoria] agardhii); gvpC16, of length 417?bp, encodes a 16?kDa protein of 139 amino acid residues that differs in lacking an internal 33-residue section. An untranslated 72?bp fragment from the 3′ end of gvpC, designated ΩC, is also present in some strains. The two types of gvpC and presence of ΩC could be distinguished by the different lengths of PCR amplification products obtained using pairs of oligonucleotide primers homologous to internal sequences in gvpC and gvpA. Three genotype classes were found: GV1, containing only gvpC20; GV2, containing gvpC20 and ΩC; and GV3, containing gvpC16, gvpC20 and ΩC. Subclasses of GV2 and GV3 contained either one or two copies of ΩC. The accompanying paper by D. I. Bright & A. E. Walsby (Microbiology 145, 2769–2775) shows that strains of the GV3 genotype produce gas vesicles with a higher critical pressure than those of GV1 and GV2. A PCR survey of 185 clonal cultures of P. rubescens isolated from Lake Zürich revealed that 3 isolates were of genotype GV1, 73 were of GV2 and 109 were of GV3. The PCR technique was used to distinguish the gas vesicle genotype, and thence the associated critical-pressure phenotype, of single filaments selected from lakewater samples. Sequence analysis of the 16S rDNA and of regions within the operons encoding phycoerythrin, phycocyanin and Rubisco confirmed that these strains of Planktothrix form a tight phylogenetic group.
机译:通过PCR从瑞士苏州苏黎世湖中分离的三种Planktothrix Rubescens扩增了气体囊泡基因簇的一部分。每个包含GVPA和GVPC的多个交替副本。不同菌株中的所有GVPA序列都是相同的。 GVPC有两种类型的GVPC:GVPC20的长度为516〜BP,编码20μl的氨基酸残基的20?KDA蛋白(其N-末端氨基酸序列与Planktothrix [振荡器] agardhii的GVPC序列同源);长度为417〜BP的GVPC16编码139个氨基酸残基的16℃蛋白质,其不同于缺少内部33-残基部分。来自GVPC的3'末端的未转换的72型BP片段,指定ωC,也存在于一些菌株中。可以通过使用GVPC和GVPA的内序对对的寡核苷酸引物获得的不同长度的PCR扩增产物来区分两种类型的GVPC和存在ωC的存在。发现了三种基因型类:GV1,仅包含GVPC20; GV2,包含GVPC20和ωc;和GV3,包含GVPC16,GVPC20和ωc。 GV2和GV3的子类包含一个或两个ωc拷贝。 D. I.伴随的纸张D.I.WALSBY(微生物学145,2769-2775)表明,GV3基因型的菌株产生的气囊,其临界压力高于GV1和GV2的临界压力。从苏明湖中分离的P. Rubescens的185个克隆培养的PCR调查显示,3个分离物是基因型Gv1,73的GV2和109的GV3。 PCR技术用于区分气体囊泡基因型,以及从湖水样品中选择的单长丝的相关临界压力表型。 16S RDNA和编码浮藻,植物植物和Rubisco的操纵子内的区域的序列分析证实,这些浮动螺纹的菌株形成了紧密的系统发育基团。

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