2004
DOI: 10.1007/s11021-005-0016-9
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Identification of Methylobacterium strains using sequence analysis of 16S rRNA genes

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Cited by 2 publications
(5 citation statements)
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“…KLDS1.0318 genomic DNA was isolated using the DNeasy Tissue kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions. The universal primer (27F/1492R) was used for PCR and the amplification conditions were as follows: initial denaturation step at 94°C for 3 min, 35 cycles of denaturation at 94°C for 30 s, annealing at 55°C for 30 s, elongation at 72°C for 1 min and final extension at 72°C for 5 min (Romanovskaya et al, 2004). The PCR product was then sent for sequencing to the Comate Bioscience Co., Ltd (Jilin, China).…”
Section: Methodsmentioning
confidence: 99%
“…KLDS1.0318 genomic DNA was isolated using the DNeasy Tissue kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions. The universal primer (27F/1492R) was used for PCR and the amplification conditions were as follows: initial denaturation step at 94°C for 3 min, 35 cycles of denaturation at 94°C for 30 s, annealing at 55°C for 30 s, elongation at 72°C for 1 min and final extension at 72°C for 5 min (Romanovskaya et al, 2004). The PCR product was then sent for sequencing to the Comate Bioscience Co., Ltd (Jilin, China).…”
Section: Methodsmentioning
confidence: 99%
“…Ltd) и агаризованное сусло. Различные экологофизиологические группы микроорганизмов выделяли на селективных средах [6], метилотрофные бактерии -на минеральной среде с метанолом (0.5%) [18].…”
Section: материалы и методыunclassified
“…Идентификацию бактерий проводили на основании изучения их морфологофизиологических свойств [6], а также используя сиквенс-анализ генов 16S рРНК. Методами, описанными в [18], из биомассы антарктических бактерий выделяли ДНК. С использованием полимеразной цепной реакции (ПЦР) получали амплифицированные гены 16S рРНК и их секвенировали.…”
Section: материалы и методыunclassified
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