="WGS of endophytic prokaryote culture - " &A3 - SRA

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SRX22532390: ="WGS of endophytic prokaryote culture - " &A3
1 ILLUMINA (NextSeq 500) run: 1.3M spots, 211M bases, 121.5Mb downloads

Design: Roots of adult trees of white poplar were collected in May 2023 in different geographical locations of the European part of Russia. The obtained plant roots were placed in zip-lock bags and transported to the laboratory at +4C for further analysis within 24 h after collection. For isolation of culturable bacteria, the roots were cut into small pieces and sterilized using surfactants and disinfectants: Tween-20 and sodium hypochlorite 3%, after application of which the root was thoroughly washed with autoclaved water. To confirm complete sterilization of the roots surface after disinfection, the roots were incubated in a Petri dish with sterile agarized Luria-Bertani (LB) nutrient medium for three days. In case of colony development on such dishes, the roots were discarded. The roots were then ground in 1 ml of phosphate-salt buffer. The resulting suspension was serially diluted and aseptically poured 0.1 ml into sterile Petri dishes with LB agar medium. Then incubated at 20 C for 48-72 h and colony growth was checked. The pure bacterial strain was obtained by isolation on fresh LB-agar plates. Strains were preserved in 30% (v/v) glycerol at -80 C until further analysis. Before DNA isolation, bacterial samples were stored at -80 C. Total DNA was isolated from bacteria using the DNeasy PowerSoil Pro DNeasy kit (Qiagen, Hilden, Germany) according to the manufacturer's protocol. DNA was quantified using a Qubit2.0 fluorometer (Thermo Fisher Scientific, Waltham, MA, USA); quality control was performed on a NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies Inc., Wilmington, DE, USA). The A260/A280 ratio in the DNA samples was 1.8-2.0. Approximately 100 ng of genomic DNA was fragmented into 500-bp-long double-stranded fragments using the Covaris S220 system (Covaris Inc., MA, USA). Double-stranded DNA library was prepared using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NewEngland Biolabs, Ipswich, MA, USA) according to the manufacturer's recommendations. AMPure XP beads were used to select DNA libraries by size (500-600 bp). Sample quantitation at standard concentration dilution to 4 nM was determined using a Qubit2.0 fluorometer (Thermo Fisher Scientific, Waltham, MA, USA) and verified on an Agilent 2100 Bioanalyzer using a highly sensitive DNA chip (Agilent Technologies). Genomic DNA of bacteriophage PhiX was used as an internal control. Sequencing was performed using the MiSeq Reagent Kit v3 (300 cycles) on Illumina's MiSeq platform according to the manufacturer's instructions. This resulted in 400 Mb of data (2 150 bp paired-end reads) for each sample. Illumina reads were trimmed from the trailing 3'-end with both fixed quality threshold and sliding window, filtered for average read quality, and adaptors were removed using the trimmomatic 0.39.

Submitted by: Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Study: Culturable bacterial endophytes of wild white poplar (Populus alba L.) roots: a first look at their biological potential

PRJNA1040149 • SRP472009 • All experiments • All runs

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White poplar (Populus alba L.) has good potential for green economy and phytoremediation. Bio-remediation using endophytic bacteria can be considered as a safe strategy to increase poplar productivity and its resistance to toxic conditions of urban environment. The aim of our work was to first investigate bacterial endophytes of wild-growing white poplar and to hypothesize their bio-remediation potential. For this purpose, we performed whole-genome sequencing of 14 bacterial strains isolated from root tissues of white poplar of different geographical origins. We then per-formed bioinformatic searches and physiological tests to characterize molecular and metabolic features that may be beneficial for poplar growth, resistance to environmental pollutants and pathogens. The identified strains belong to the genera Bacillus, Corynebacterium, Kocuria, Micrococcus, Peribacillus, Pseudomonas and Staphylococcus. The genomes of the strains contain genes involved in enhanced metabolism of nitrogen, phosphorus, metals, synthesis of plant hormones, and detoxifi-cation of heavy metals and organic pollutants. All strains are able to grow on media without ni-trogen sources, which indicates their ability to fix atmospheric nitrogen. It is concluded that the best biological potential is possessed by strains belonging to the genus Pseudomonas and bacteria of the species Kocuria rosea.

Sample: s3 - Staphylococcus haemolyticus PFO2

SAMN38245986 • SRS19542449 • All experiments • All runs

Organism: Staphylococcus haemolyticus

Library:

Name: s3 - Staphylococcus haemolyticus PFO2

Instrument: NextSeq 500

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Runs: 1 run, 1.3M spots, 211M bases, 121.5Mb

Run	# of Spots	# of Bases	Size	Published
SRR26836472	1,277,307	211M	121.5Mb	2024-12-05

ID:: 30524451

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