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Bacterial diversity in Adelie penguin, Pygoscelis adeliae, guano: molecular and morpho-physiological approaches

机译:鸟粪阿德利企鹅,阿德利企鹅的细菌多样性:分子和形态生理学方法

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The total number of bacteria and culturable bacteria in Adelie penguin (Pygoscelis adeliae) guano was determined during 42 days of decomposition in a location adjacent to the rookery in Admiralty Bay, King George Island, Antarctica. Of the culturable bacteria, 72 randomly selected colonies were described using 49 morpho-physiological tests, 27 of which were subsequently considered significant in characterizing and differentiating the isolates. On the basis of the nucleotide sequence of a fragment of the 16S rRNA gene in each of 72 pure isolates, three major phylogenetic groups were identified, namely the Moraxellaceae/Pseucloinonadaceae (29 isolates), the Flavobacteriaceae (14), and the Micrococcaceae (29). Grouping of the isolates on the basis of morpho-physiological tests (whether 49 or 27 parameters) showed similar results to those based on 16S rRNA gene sequences. Clusters were characterized by considerable intra-cluster variation in both 16S rRNA gene sequences and morpho-physiological responses. High diversity in abundance and morphometry of total bacterial communities during penguin guano decomposition was supported by image analysis of epifluorescence micrographs. The results indicate that the bacterial community in penguin guano is not only one of the richest in Antarctica, but is extremely diverse, both phylogenetically and morpho-physiologically. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
机译:在分解后的42天中,确定了南极乔治国王岛金钟湾群附近某个位置的阿德利企鹅(Pygoscelis adeliae)鸟粪中的细菌总数和可培养细菌总数。在可培养细菌中,使用49种形态生理学测试描述了72个随机选择的菌落,其中27种随后被认为在表征和区分分离物中具有重要意义。根据72个纯分离株中16S rRNA基因片段的核苷酸序列,确定了三个主要的系统发育组,即莫拉氏菌/假单胞菌科(29个分离株),黄杆菌科(14个)和微球菌科(29个)。 )。根据形态生理学测试(无论是49个参数还是27个参数)对分离株进行分组显示的结果与基于16S rRNA基因序列的结果相似。簇的特征是在16S rRNA基因序列和形态生理反应中簇内差异很大。落射荧光显微照片的图像分析支持了企鹅鸟粪分解过程中总细菌群落的丰度和形态的高度多样性。结果表明,企鹅鸟粪中的细菌群落不仅是南极洲最丰富的群落之一,而且在系统发育和形态生理上都极为多样。 (C)2004年欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。

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