Soil microbiome (Bacteria) on Keller Peninsula (Antarctica)

Последняя версия опубликована SCAR - Microbial Antarctic Resource System Mar 19, 2019 SCAR - Microbial Antarctic Resource System

Amplicon sequencing dataset (454 pyrosequencing and Ion Torrent) of Bacteria (16S ssu rRNA gene) in ice-free soils of Keller Peninsula (Antarctica)


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Как оформить ссылку

Исследователи должны дать ссылку на эту работу следующим образом:

Roesch L, Fulthorpe R, Pereira A, Pereira C, Lemos L, Barbosa A, Suleiman A, Gerber A, Pereira M, Loss A, de Costa E (2019): Soil microbiome (Bacteria) on Keller Peninsula (Antarctica). v1.1. SCAR - Microbial Antarctic Resource System. Dataset/Metadata.


Исследователи должны соблюдать следующие права:

Публикующей организацией и владельцем прав на данную работу является SCAR - Microbial Antarctic Resource System. This work is licensed under a Creative Commons Attribution (CC-BY) 4.0 License.

Регистрация в GBIF

Этот ресурс был зарегистрирован в GBIF, ему был присвоен следующий UUID: 48350841-8927-4c78-bbc1-24c01a4d5586.  SCAR - Microbial Antarctic Resource System отвечает за публикацию этого ресурса, и зарегистрирован в GBIF как издатель данных при оподдержке Scientific Committee on Antarctic Research.

Ключевые слова



Кто является создателем ресурса:

Luiz Roesch
Universidade Federal do Pampa Sao Gabriel BR
Roberta Fulthorpe
University of Toronto at Scarborough Scarborough CA
Antonio Pereira
Universidade Federal do Pampa Sao Gabriel BR
Clarissa Pereira
Universidade Federal do Pampa Sao Gabriel BR
Leondro Lemos
Universidade Federal do Pampa Sao Gabriel BR
Anthony Barbosa
Universidade Federal do Pampa Sao Gabriel BR
Afnan Suleiman
Universidade Federal do Pampa Sao Gabriel BR
Alexandra Gerber
Unidade de Genômica Computacional Darcy Fontoura de Almeida Rio de Janeiro BR
Marcos Pereira
Universidade Federal Rural do Rio de Janeiro Rio de Janeiro BR
Arcangelo Loss
Universidade Federal Rural do Rio de Janeiro Rio de Janeiro BR
Elias de Costa
Universidade Federal Rural do Rio de Janeiro Rio de Janeiro BR

Кто может ответить на вопросы о ресурсе:

Luiz Roesch
Universidade Federal do Pampa Sao Gabriel BR

Кем заполнены метаданные:

Maxime Sweetlove
research assistent
Royal Belgian Institute of Natural Sciences Rue Vautier 29 1000 Brussels BE

Кто еще связан с данным ресурсом:


Географический охват

Keller Peninsula, Antarctica

Ограничивающие координаты Юг Запад [-64.294, -58.482], Север Восток [-62.062, -56.691]

Таксономический охват

Bacteria, based on the 16S ssu rRNA gene

Domain  Bacteria (Bacteria)

Временной охват

Период формирования 2009-2010

Данные проекта

Описание отсутсвует

Название Soil microbiome (Bacteria) on Keller Peninsula (Antarctica)
Финансирование This work was supported by the INCT-APA (CNPq process No. 574018/2008-5, FAPERJ E-26/170.023/2008) and Ministry of Science and Technology, and the Secretariat for the Marine Resources Interministerial Committee (SECIRM). Additional funding was provided via a fellowships from the CNPq (process number 503370/2009-6).

Исполнители проекта:

Luiz Roesch

Методы сбора

A total of 12 soil samples were chosen for sampling and were taken from a variety of plant communities having different soil features. Soil was collected removing the plant cover and taking cores of 5 cm diameter and 5 cm depth. All soil was stored on ice upon collection and transported to the laboratory for extraction.

Охват исследования Soil samples were collected on the Keller Peninsula, King George Island, Antarctica during the austral summer of 2009–2010.

Описание этапа методики:

  1. DNA was isolated from at least 1 g of mixed soil using the PowerSoilTM DNA Isolation Kit (MO BIO) as described by the manufacturer. The genomic DNA concentration and purity were determined by spectrophotometry.
  2. Twelve independent PCR reactions were performed for each soil sample with the primers 338R and 27F for the amplification of the V1–V2 hypervariable regions of the 16S rRNA gene. PCR was performed with the GoTaq PCR core system (Promega, Madi- son, WI, USA). The mixtures contained 5 ul of 10× PCR buffer, 200 mM dNTPs, 100 mM of each primer, 2.5 U of Taq polymerase and approximately 100ng of DNA template in a final volume of 50 ul. The PCR conditions were 94 ◦ C for 2 min, 30 cycles of 94◦C for 45s; 55◦C for 45s; and 72◦C for 1min extension; followed by 72 ◦C for 6 min. The 16S rRNA gene fragments were sequenced using 454 GS FLX Titanium (Lib-L) chemistry for unidirectional sequencing of the amplicon libraries. Barcoded primers were used to multiplex the amplicon pools so they could be sequenced together and computationally separated afterward. To do this, 8-base barcodes were added to the 5′-end of the reverse primers using the self-correcting barcode method of Hamady et al. (2008). The primers were attached to the GS FLX Titanium Primer A (5′ -CCATCTCATCCCTGCGTGTCTCCGACTCAG-3′ ) and Primer B (5′ - CCTATCCCCTGTGTGCCTTGGCAGTC-3′ ) sequences, modified for use with GS FLX Titanium emPCR Kits (Lib-L) and a two-base linker sequence was inserted between the 454 adapter and the 16S rRNA primers to reduce any effect the composite primer might have on PCR efficiency. The PCR products for each of the 12 samples were purified and combined in equimolar ratios with the quantitative DNA binding method (SequalPrep Kit, Invitrogen, Carlsbad, CA, USA) to create a DNA pool that was used for pyrosequencing from the A-Key adaptor.

Библиографические ссылки

  1. Roesch, L. F., Fulthorpe, R. R., Pereira, A. B., Pereira, C. K., Lemos, L. N., Barbosa, A. D., ... & da Costa, E. M. (2012). Soil bacterial community abundance and diversity in ice-free areas of Keller Peninsula, Antarctica. Applied soil ecology, 61, 7-15.|Rampelotto, P. H., Barboza, A. D. M., Pereira, A. B., Triplett, E. W., Schaefer, C. E. G., de Oliveira Camargo, F. A., & Roesch, L. F. W. (2015). Distribution and interaction patterns of bacterial communities in an ornithogenic soil of Seymour Island, Antarctica. Microbial ecology, 69(3), 684-694.

Дополнительные метаданные

Альтернативные идентификаторы 48350841-8927-4c78-bbc1-24c01a4d5586