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Introduction of a novel 18S rDNA gene arrangement along with distinct ITS region in the saline water microalga Dunaliella

机译:在盐水微藻杜氏藻中引入新的18S rDNA基因排列以及独特的ITS区

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Comparison of 18S rDNA gene sequences is a very promising method for identification and classification of living organisms. Molecular identification and discrimination of different Dunaliella species were carried out based on the size of 18S rDNA gene and, number and position of introns in the gene. Three types of 18S rDNA structure have already been reported: the gene with a size of ~1770 bp lacking any intron, with a size of ~2170 bp consisting one intron near 5' terminus, and with a size of ~2570 bp harbouring two introns near 5' and 3' termini. Hereby, we report a new 18S rDNA gene arrangement in terms of intron localization and nucleotide sequence in a Dunaliella isolated from Iranian salt lakes (ABRIINW-M1/2). PCR amplification with genus-specific primers resulted in production of a ~2170 bp DNA band, which is similar to that of D. salina 18S rDNA gene containing only one intron near 5' terminus. Whilst, sequence composition of the gene revealed the lack of any intron near 5' terminus in our isolate. Furthermore, another alteration was observed due to the presence of a 440 bp DNA fragment near 3' terminus. Accordingly, 18S rDNA gene of the isolate is clearly different from those of D. salina and any other Dunaliella species reported so far. Moreover, analysis of ITS region sequence showed the diversity of this region compared to the previously reported species. 18S rDNA and ITS sequences of our isolate were submitted with accesion numbers of EU678868 and EU927373 in NCBI database, respectively. The optimum growth rate of this isolate occured at the salinity level of 1 M NaCl. The maximum carotenoid content under stress condition of intense light (400 μmol photon m-2 s-1), high salinity (4 M NaCl) and deficiency of nitrate and phosphate nutritions reached to 240 ng/cell after 15 days.
机译:18S rDNA基因序列的比较是一种非常有前途的生物鉴定和分类方法。根据18S rDNA基因的大小以及该基因中内含子的数量和位置,对杜氏藻的不同种类进行了分子鉴定和判别。已经报道了三种类型的18S rDNA结构:约1770 bp的基因缺少任何内含子,约2170 bp的基因在5'末端附近包含一个内含子,约2570 bp的基因带有两个内含子5'和3'总站附近。据此,我们报道了从伊朗盐湖(ABRIINW-M1 / 2)分离出的杜氏藻内含子定位和核苷酸序列方面的新18S rDNA基因排列。用属特异性引物进行PCR扩增可产生约2170 bp的DNA条带,这与D. salina 18S rDNA基因在5'末端仅含一个内含子的相似。同时,该基因的序列组成表明我们的分离物中5'末端附近没有任何内含子。此外,由于在3'末端附近存在440 bp DNA片段,观察到另一种改变。因此,分离物的18S rDNA基因与盐藻和迄今报道的任何其他杜氏藻明显不同。此外,与先前报道的物种相比,ITS区域序列分析显示了该区域的多样性。我们分离株的18S rDNA和ITS序列分别在NCBI数据库中提交,保藏号为EU678868和EU927373。该分离物的最佳生长速率出现在1 M NaCl的盐度水平。强光(400μmol光子m -2 s -1 ),高盐度(4 M NaCl)和缺乏硝酸盐和磷酸盐营养的胁迫条件下的最大类胡萝卜素含量15天后达到240 ng / cell。

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