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2
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77957826989
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(a) Cao, S.; Ross, L.; Tamayo, G.; Clardy, J. Org. Lett. 2010, 12, 4661-4663;
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(2010)
Org. Lett.
, vol.12
, pp. 4661-4663
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Cao, S.1
Ross, L.2
Tamayo, G.3
Clardy, J.4
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4
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79953219129
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Sequencing and species identification. For identification by internal transcribed spacer (ITS) sequencing, CR237A and CR1092F were cultured in potato dextrose broth for 5 days. The mycelium was then retrieved by filtration and ground to a fine powder in liquid N2. Genomic DNA was extracted using the Wizard Genomic DNA Purification Kit (Promega), and large subunit rDNA was amplified by PCR using primers LR5 (5′-TCCTGAGGGAAACTTCG-3′) and LROR (5′-ACCCGCTGAACTTAAGC-3′). PCR products were transformed into E. coli TOP10 cells using a TOPO TA Cloning Kit (Invitrogen), according to manufacturer's protocols
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Sequencing and species identification. For identification by internal transcribed spacer (ITS) sequencing, CR237A and CR1092F were cultured in potato dextrose broth for 5 days. The mycelium was then retrieved by filtration and ground to a fine powder in liquid N2. Genomic DNA was extracted using the Wizard Genomic DNA Purification Kit (Promega), and large subunit rDNA was amplified by PCR using primers LR5 (5′-TCCTGAGGGAAACTTCG-3′) and LROR (5′-ACCCGCTGAACTTAAGC-3′). PCR products were transformed into E. coli TOP10 cells using a TOPO TA Cloning Kit (Invitrogen), according to manufacturer's protocols. Transformed plasmids were isolated and sequenced at Genewiz (http://www.genewiz.com/). The following consensus sequence were used in a BLAST search against deposited sequences: 237A: CCCCTATGCCCAAATTTGACGATCGATTTGCACGTCAGAACCGCTGCGAGCCT CCACCAGAGTTTCCTCTGGCTTCACCCTATTCAGGCATAGTTCACCATCTTTCGGGTC CCAACAGCTATGCTCTTACTCAAATCCATCCGAAGACATCAGGATCGGTCGATGGTG CGCCAGAGCTCGCGCCCTGGGTCCCACCTCCGTTCACTTTCATTCCGCGCCCGGGCTT GACACCCAAACACTCGCATAGATGTTAGACTCCTTGGTCCGTGTTTCAAGACGGGCC GCTTACGACCATTACGCCAGCATCCTAGCCGAAGCGCGGACCTCAGTCGGGGCTGG CTGCATGACGCCCTGGGCTATAACACTCCCCGAAGAGAGCTACATTCCCAAGGCCTT TCTCCAGCCGCCCCAACTGATGCTGGCCTGCCTGCCGCCGAGTGCACAGGGGACGG ACCCCCGATGAACAGCGGCAGCCAAGTCTGGTTGCAAGCGCTTCCCTTTCAACAATT TCACGTGCTGTTTGACTCTCTTTCCAAAGTGCTTTTCATCTTTCGATCACTCTACTTGT GCGCTATCGGTCTCTGGCCAGTATTTAGCTTTAGAAGAAATATACCTCCCATTTAGA GCTGCATTCCCAAACAACTCGACTCGTCGAAGGGGGTTCACATGGCGCAGGCACCTG CCGCGTACGGGGTTCTCACCCTCTCTGACGTCCCGTTCCAAGGAACTTAGACAGGCGN CGTTGCCGAACCACCNTCTGCAAAGTACAACTCGGANCCCGCAAGGAGCCAGATTTC AAATTTGAGCTGTTGCCGCTTCACTCGCCGTTACT GAGGCAAT CR1092F: AGAGGTTGATAGTCTTTGCCCCCATGCTCATGTTTGACGATCGATTTGCA CGTCAGAACCGCTGCGAGCCTCCACCAGAGTTTCCTCTGGCTTCACCCTACACAAGC ATAGTTCACCATCTTTCGGGTCCAAGCGGCAAGGCTCTTACTCAAATCCATCCGAAG ACTTCAGGATCGGTCGATGGTGCGCCGAmAGAGGTTGATAGTCTTTCGCCCCCATG CTCATGTTTGACGATCGATTTGCACGTCAGAACCGCTGCGAGCCTCCACCAGAGTTT CCTCTGGCTAGAGGTTGATAGTCTTTCGCCCCCATGCTCATGTTTGACGATCGATTTG CACGTCAGAACCGCTGCGAGCCTCCACCAGAGTTTCCTCTGGCTTCACCCTACACAA GCATAGTTCACCATCTTTCGGGTCCAAGCGGCAAGGCTCTTACTCAAATCCATCCGA AGACTTCAGGATCGGTCGATGGTGCGCCGAmAGAGGTTGATAGTCTTTCGCCCCCA TGCTCATGTTTGACGATCGATTTGCACGTCAGAACCGCTGCGAGCCTCCACCAGAGT TTCCTCTGGCTAGAGGTTGATAGTCTTTCGCCCCCATGCTCATGTTTGACGATCGATT TGCACGTCAGAACCGCTGCGAGCCTCCACCAGAGTTTCCTCTGGCTTCACCCTACAC AAGCATAGTTCACCATCTTTCGGGTCCAAGCGGCAAGGCTCTTACTCAAATCCATCC GAAGACTTCAGGATCGGTCGATGGTGCGCCGAmAGAGGTTGATAGTCTTTCGCCCC CATGCTCATGTTTGACGATCGATTTGCACGTCAGAACCGCTGCGAGCCTCCACCAGA GTTTCCTCTGGCT AGAGGTT TTTCAANCGGGGTAA.
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6
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79953170633
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note
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R: 9.5 min, 2.0 mg; C-18, Phemonenex, Luna, 250 x 10 mm, 5 μ, 2 ml/min, 60-100% MeOH in 20 min).
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7
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44949281225
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Venkatasubbaiah, P.; Van Dyke, C. G.; Chilton, W. S. Phytochemistry 1991, 30, 1471-1474.
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(1991)
Phytochemistry
, vol.30
, pp. 1471-1474
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Venkatasubbaiah, P.1
Van Dyke, C.G.2
Chilton, W.S.3
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8
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79953182037
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note
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6, 387.1808).
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9
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79953200879
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note
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6, 373.1651).
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10
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79953227770
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note
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5, 239.0920).
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11
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79953200214
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note
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2 Briefly, extracts dissolved in DMSO were arrayed in dilution series in 384-well plates. The solutions were pintransferred to assay plates containing red blood cells parasitized with Plasmodium falciparum. A fluorescent DNA stain (DAPI) was added after a 72 h incubation period, and the plates imaged to quantify levels of parasitic nuclei.
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