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利用实时聚合酶链反应对原绿球藻生态型进行测量,结果显示具有相似光生理特性的基因型丰度不同。

Measurement of Prochlorococcus ecotypes using real-time polymerase chain reaction reveals different abundances of genotypes with similar light physiologies.

作者信息

Ahlgren Nathan A, Rocap Gabrielle, Chisholm Sallie W

机构信息

Department of Civil and Environmental Engineering, Massachusetts Institute of Technology 48-425, Cambridge, MA 02139, USA.

出版信息

Environ Microbiol. 2006 Mar;8(3):441-54. doi: 10.1111/j.1462-2920.2005.00910.x.

Abstract

Prochlorococcus is a marine cyanobacterium which is found at high abundances in world's tropical and subtropical oligotrophic oceans. The genus Prochlorococcus can be divided into two major groups based on light physiology. Both of these groups can be further subdivided into genetically distinct lineages, or ecotypes. Real-time polymerase chain reaction (PCR) assays based on sequence differences in the 16S-23S rDNA internal transcribed spacer or the 23S rDNA were developed to examine the distribution of each ecotype in the field. The real-time PCR assays enabled linear quantification of concentrations ranging from 10 to 4 x 10(5) cells ml(-1). These assays were applied to a stratified water column in the Sargasso Sea. The majority of Prochlorococcus cells above 110 m belonged to the one of the low chlorophyll b/a ratio (high-light adapted) ecotypes, while two types of high chlorophyll b/a ratio (low-light adapted) cells dominated below 110 m. The other three types were found at significantly lower numbers or not detected at all. Differences in the abundance of ecotypes within the major light physiology groupings suggest that other factors, such as nutrient utilization and differential mortality, are driving their relative distributions. Real-time PCR assays will enable further exploration of these factors and temporal and geographic variability in ecotype abundance.

摘要

原绿球藻是一种海洋蓝细菌,在世界热带和亚热带贫营养海洋中大量存在。根据光生理学,原绿球藻属可分为两个主要类群。这两个类群都可进一步细分为基因上不同的谱系,即生态型。基于16S - 23S rDNA内部转录间隔区或23S rDNA序列差异的实时聚合酶链反应(PCR)检测方法被开发出来,用于研究各生态型在野外的分布。实时PCR检测能够对浓度范围从10到4×10⁵个细胞/毫升进行线性定量。这些检测方法被应用于马尾藻海的分层水柱。在110米以上,大多数原绿球藻细胞属于低叶绿素b/a比值(高光适应)生态型之一,而在110米以下,两种高叶绿素b/a比值(低光适应)细胞占主导地位。其他三种类型的细胞数量显著较少或根本未被检测到。主要光生理学分组内生态型丰度的差异表明,其他因素,如养分利用和不同的死亡率,正在推动它们的相对分布。实时PCR检测将有助于进一步探索这些因素以及生态型丰度的时间和地理变异性。

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