Glaeser Jens, Overmann Jörg
Bereich Mikrobiologie, Department I, Ludwig-Maximilians-Universität München, Maria-Ward-Strasse 1a, D-80638 Munich, Germany.
Appl Environ Microbiol. 2003 Jul;69(7):3739-50. doi: 10.1128/AEM.69.7.3739-3750.2003.
A dense population of the phototrophic consortium "Pelochromatium roseum" was investigated in the chemocline of a temperate holomictic lake (Lake Dagow, Brandenburg, Germany). Fluorescence in situ hybridization revealed that the brown epibionts of "P. roseum" constituted up to 37% of the total bacterial cell number and up to 88% of all green sulfur bacteria present in the chemocline. Specific amplification of 16S rRNA gene fragments of green sulfur bacteria and denaturing gradient gel electrophoresis fingerprinting yielded a maximum of four different DNA bands depending on the year of study, indicating that the diversity of green sulfur bacteria was low. The 465-bp 16S rRNA gene sequence of the epibiont of "P. roseum" was obtained after sorting of individual consortia by micromanipulation, followed by a highly sensitive PCR. The sequence obtained represents a new phylotype within the radiation of green sulfur bacteria. Maximum light-dependent H(14)CO(3)(-) fixation in the chemocline in the presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea suggested that there was anaerobic autotrophic growth of the green sulfur bacteria. The metabolism of the epibionts was further studied by determining stable carbon isotope ratios (delta(13)C) of their specific biomarkers. Analysis of photosynthetic pigments by high-performance liquid chromatography revealed the presence of high concentrations of bacteriochlorophyll (BChl) e and smaller amounts of BChl a and d and chlorophyll a in the chemocline. Unexpectedly, isorenieratene and beta-isorenieratene, carotenoids typical of other brown members of the green sulfur bacteria, were absent. Instead, four different esterifying alcohols of BChl e were isolated as biomarkers of green sulfur bacterial epibionts, and their delta(13)C values were determined. Farnesol, tetradecanol, hexadecanol, and hexadecenol all were significantly enriched in (13)C compared to bulk dissolved and particulate organic carbon and compared to the biomarkers of purple sulfur bacteria. The difference between the delta(13)C values of farnesol, the major esterifying alcohol of BChl e, and CO(2) was -7.1%, which provides clear evidence that the mode of growth of the green sulfur bacterial epibionts of "P. roseum" in situ is photoautotrophic.
在一个温带完全混合湖泊(德国勃兰登堡州达戈湖)的化学分层中,对光合菌群“玫瑰色佩洛色菌”的密集种群进行了研究。荧光原位杂交显示,“玫瑰色佩洛色菌”的棕色外共生体占细菌细胞总数的比例高达37%,占化学分层中所有绿色硫细菌的比例高达88%。根据研究年份的不同,对绿色硫细菌的16S rRNA基因片段进行特异性扩增和变性梯度凝胶电泳指纹分析,最多可产生四条不同的DNA条带,这表明绿色硫细菌的多样性较低。通过显微操作对单个菌群进行分选,然后进行高灵敏度PCR,获得了“玫瑰色佩洛色菌”外共生体的465 bp 16S rRNA基因序列。所获得的序列代表了绿色硫细菌辐射范围内的一个新系统型。在存在3-(3,4-二氯苯基)-1,1-二甲基脲的情况下,化学分层中最大的光依赖性H(14)CO(3)(-)固定表明绿色硫细菌存在厌氧自养生长。通过测定其特定生物标志物的稳定碳同位素比率(δ(13)C),进一步研究了外共生体的代谢。通过高效液相色谱分析光合色素发现,化学分层中存在高浓度的细菌叶绿素(BChl)e以及少量的BChl a、d和叶绿素a。出乎意料的是,绿色硫细菌其他棕色成员典型的类胡萝卜素异壬二烯和β-异壬二烯并不存在。相反,分离出了四种不同的BChl e酯化醇作为绿色硫细菌外共生体的生物标志物,并测定了它们的δ(13)C值。与溶解态和颗粒态总有机碳以及紫色硫细菌的生物标志物相比,法尼醇、十四烷醇、十六烷醇和十六碳烯醇的(13)C均显著富集。BChl e的主要酯化醇法尼醇的δ(13)C值与CO(2)之间的差值为-7.1%,这清楚地证明了原位“玫瑰色佩洛色菌”绿色硫细菌外共生体的生长模式是光合自养型。