22 research outputs found
A cross-cultural study of domestic luminous environment in the United Kingdom and Japan
Abstract not available
Morphological characterization of <i>Scheffersomyces henanensis</i> sp. nov. BY-41<sup>T</sup>.
<p>(a) Budding cells grown on YM broth for 3 days at 25°C. (b) Asci formed on cornmeal agar after 6 days at 25°C. Bar, 10 μm.</p
GenBank accession numbers of the nucleotide sequences used in this study<sup>*</sup>.
<p>*Sequences generated in this work shown in bold. <sup>T</sup>  =  type strain.</p
Nucleotide differences and percentages of homology between <i>Scheffersomyces henanensis</i> sp. nov. and the type cultures of closest relatives, S. <i>segobiensis</i>, <i>S</i>. <i>stipitis</i> and <i>S. illinoinensis</i>.
<p>Nucleotide differences and percentages of homology between <i>Scheffersomyces henanensis</i> sp. nov. and the type cultures of closest relatives, S. <i>segobiensis</i>, <i>S</i>. <i>stipitis</i> and <i>S. illinoinensis</i>.</p
Physiological characteristics of <i>Scheffersomyces henanensis</i> sp. nov.<sup>*</sup>
<p>*Symbols: +, Positive; –, negative; D, delayed positive; and W, weakly positive.</p
Phylogenetic tree constructed from neighbour-joining analysis of the combined sequences of SSU, ITS, D1/D2 LUS and <i>RPB1</i>, depicting the relationships of <i>Scheffersomyces henanensis</i> sp. nov. with closely related taxa in the <i>Scheffersomyces</i> clade.
<p><i>Candida tropicalis</i> was used as an outgroup taxon (in gray). Bootstrap percentages over 50% from 1000 bootstrap replicates are shown. Bar, 0.01 substitutions per nucleotide position.</p
Phylogenetic tree reconstructed from neighbour-joining analysis of <i>XYL1</i> sequences depicting the relationships of <i>Scheffersomyces henanensis</i> sp. nov. with closely related taxa in <i>S</i>. <i>stipitis</i> subclade.
<p><i>Scheffersomyces ergatensis</i> was used as an outgroup taxon (in grey). Numbers above each branch refer to bootstrap values out of 1000 repetitions. Bar, 0.02 substitutions per nucleotide position.</p
Physiological characteristics that differentiate <i>H. nanyangensis</i> sp. nov. from <i>C. insectamans</i><sup>a</sup>.
a<p>+, Positive; −, negative; s, slowly positive; and w, weakly positive.</p>b<p>Data from <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0103737#pone.0103737-Lachance1" target="_blank">[35]</a>.</p
Physiological characteristics and other growth tests of <i>H. nanyangensis</i> sp. nov.<sup>a</sup>
a<p>+, Positive; −, negative; and w, weakly positive.</p
Phylogenetic tree constructed by maximum likelihood analysis based on the combined gene sequences of the nearly entire SSU rRNA and D1/D2 domain of LSU rRNA depicting the placement of <i>Hemisphaericaspora nanyangensis</i> sp. nov. and representative neighbouring taxa in the family Debaryomycetaceae [2], [12], [30].
<p>Bootstrap values above 50% are given at nodes based on 1,000 replications. The sequence accession numbers are shown in parentheses with the first number representing SSU rRNA gene and the second representing D1/D2 LSU rRNA gene. Bar, 0.01 substitutions per nucleotide position. <i>Schizosaccharomyces pombe</i> NRRL Y-12796<sup>T</sup> was used as an outgroup.</p