Baker Kristopher M, Gobler Christopher J, Collier Jackie L
School of Marine and Atmospheric Sciences, Stony Brook University, Stony Brook, New York 11794-5000, USA.
J Phycol. 2009 Jun;45(3):625-34. doi: 10.1111/j.1529-8817.2009.00680.x. Epub 2009 May 21.
While urea has long been recognized as an important form of nitrogen in planktonic ecosystems, very little is known about how many or which phytoplankton and bacteria can use urea as a nitrogen source. We developed a method, targeting the gene encoding urease, for the direct detection and identification of ureolytic organisms and tested it on seven axenic phytoplankton cultures (three diatoms, two prymnesiophytes, a eustigmatophyte, and a pelagophyte) and on three nonaxenic Aureococcus anophagefferens Hargraves et Sieburth cultures (CCMP1784 and two CCMP1708 cultures from different laboratories). The urease amplicon sequences from axenic phytoplankton cultures were consistent with genomic data in the three species for which both were available. Seven of 12 phytoplankton species have one or more introns in the amplified region of their urease gene(s). The 63 urease amplicons that were cloned and sequenced from nonaxenic A. anophagefferens cultures grouped into 17 distinct sequence types. Eleven types were related to α-Proteobacteria, including three types likely belonging to the genus Roseovarius. Four types were related to γ-Proteobacteria, including two likely belonging to the genus Marinobacter, and two types were related to β-Proteobacteria. Terminal restriction fragment length polymorphism (TRFLP) analyses suggested that the sequenced amplicons represented approximately half of the diversity of bacterial urease genes present in the nonaxenic cultures. While many of the bacterial urease sequence types were apparently lab- or culture-specific, others were found in all three nonaxenic cultures, suggesting the possibility of specific relationships between these bacteria and A. anophagefferens.
虽然尿素长期以来一直被认为是浮游生态系统中氮的一种重要形式,但对于有多少种或哪些浮游植物和细菌能够利用尿素作为氮源,人们却知之甚少。我们开发了一种针对脲酶编码基因的方法,用于直接检测和鉴定尿素分解生物,并在七种无菌浮游植物培养物(三种硅藻、两种定鞭藻、一种真眼点藻和一种pelagophyte)以及三种非无菌的哈氏赤潮藻(Aureococcus anophagefferens Hargraves et Sieburth)培养物(CCMP1784以及来自不同实验室的两种CCMP1708培养物)上进行了测试。来自无菌浮游植物培养物的脲酶扩增子序列与三种有基因组数据的物种的基因组数据一致。12种浮游植物物种中有7种在其脲酶基因的扩增区域有一个或多个内含子。从非无菌的哈氏赤潮藻培养物中克隆并测序的63个脲酶扩增子分为17种不同的序列类型。11种类型与α-变形菌有关,包括三种可能属于玫瑰色杆菌属(Roseovarius)的类型。四种类型与γ-变形菌有关,包括两种可能属于海杆菌属(Marinobacter)的类型,还有两种类型与β-变形菌有关。末端限制性片段长度多态性(TRFLP)分析表明,测序的扩增子约占非无菌培养物中存在的细菌脲酶基因多样性的一半。虽然许多细菌脲酶序列类型显然是实验室或培养物特有的,但其他类型在所有三种非无菌培养物中都有发现,这表明这些细菌与哈氏赤潮藻之间可能存在特定关系。