2021
DOI: 10.1007/s11802-021-4965-z
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Morphology and Molecular Phylogeny of Two Marine Folliculinid Ciliates Found in China (Ciliophora, Heterotrichea)

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Cited by 7 publications
(2 citation statements)
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“…Genomic DNA was extracted from the single cleaned cell using a DNeasy Blood & Tissue Kit (QIAGEN, Hilden, Germany) following the manufacturer's instructions but modified by using 1/4 of the suggested volume for each solution (Chi et al 2022a). SSU rDNA was amplified using Q5 Hot Start high-fidelity DNA polymerase (NEB, Ipswich, MA, USA) with the universal eukaryotic primers, 18 s-F (5'-AAC CTG GTT GAT CCT GCC AGT-3') and 18 s-R (5'-TGA TCC TTC TGC AGG TTC ACC TAC -3') (Medlin et al 1988;Ye et al 2021b). PCR amplifications were according to the following procedure: 1 cycle of initial denaturation at 98 ℃ for 30 s, followed by 18 cycles of amplification (98 ℃, 10 s; 69-51 ℃ touchdown, 30 s; 72 ℃, 1 min), and another 18 cycles (98 ℃, 10 s; 51 ℃, 30 s; 72 ℃, 1 min), with a final extension of 72 ℃ for 5 min (Ma et al 2022b;Zhang et al 2022b).…”
Section: Dna Extraction and Gene Sequencingmentioning
confidence: 99%
“…Genomic DNA was extracted from the single cleaned cell using a DNeasy Blood & Tissue Kit (QIAGEN, Hilden, Germany) following the manufacturer's instructions but modified by using 1/4 of the suggested volume for each solution (Chi et al 2022a). SSU rDNA was amplified using Q5 Hot Start high-fidelity DNA polymerase (NEB, Ipswich, MA, USA) with the universal eukaryotic primers, 18 s-F (5'-AAC CTG GTT GAT CCT GCC AGT-3') and 18 s-R (5'-TGA TCC TTC TGC AGG TTC ACC TAC -3') (Medlin et al 1988;Ye et al 2021b). PCR amplifications were according to the following procedure: 1 cycle of initial denaturation at 98 ℃ for 30 s, followed by 18 cycles of amplification (98 ℃, 10 s; 69-51 ℃ touchdown, 30 s; 72 ℃, 1 min), and another 18 cycles (98 ℃, 10 s; 51 ℃, 30 s; 72 ℃, 1 min), with a final extension of 72 ℃ for 5 min (Ma et al 2022b;Zhang et al 2022b).…”
Section: Dna Extraction and Gene Sequencingmentioning
confidence: 99%
“…To remedy eutrophication by nitrogen and phosphorus in nearshore aquaculture water, scholars have actively explored methods [9,10] such as algal-bacterial symbiosis [11], higher aquatic plants [12][13][14], microalgae [15], and physicochemical methods [16,17]. Among them, the use of seaweed cultivation for controlling eutrophication has been recently proved practical [18,19].…”
Section: Introductionmentioning
confidence: 99%