2019
DOI: 10.3897/mycokeys.54.35018
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Cacaoporus, a new Boletaceae genus, with two new species from Thailand

Abstract: We introduce a new genus, Cacaoporus, characterised by chocolate brown to dark brown basidiomata and hymenophore, tubes not separable from the pileus context, white to off-white basal mycelium, reddening when bruised, amygdaliform to ovoid spores and dark brown spore deposit. Phylogenetic analyses of a four-gene dataset (atp6, tef1, rpb2 and cox3) with a wide selection of Boletaceae showed that the new genus is monophyletic and sister to the genera Cupreoboletus and Cyanoboletus in the Pulveroboletus group. Tw… Show more

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Cited by 25 publications
(23 citation statements)
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References 45 publications
(54 reference statements)
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“…PCR conditions were the same as in Raspé et al (2016). Part of the mitochondrial gene cox 3 was amplified with the primers COX3M1-F and COX3M1-R (Vadthanarat et al 2019), using KAPA2G™ Robust HotStart polymerase (Kapa Biosystems, Wilmington, MA, USA) and the following PCR programme: 2 min 30 s at 95 °C; 35 cycles of 25 s at 95 °C, 30 s at 48 °C, 30 s at 72 °C; 3 min at 72 °C. PCR products were purified by adding 1 U of Exonuclease I and 0.5 U FastAP Alkaline Phosphatase (Thermo Scientific, St. Leon-Rot, Germany) and incubated at 37 °C for 1 h, followed by inactivation at 80 °C for 15 min.…”
Section: Methodsmentioning
confidence: 99%
“…PCR conditions were the same as in Raspé et al (2016). Part of the mitochondrial gene cox 3 was amplified with the primers COX3M1-F and COX3M1-R (Vadthanarat et al 2019), using KAPA2G™ Robust HotStart polymerase (Kapa Biosystems, Wilmington, MA, USA) and the following PCR programme: 2 min 30 s at 95 °C; 35 cycles of 25 s at 95 °C, 30 s at 48 °C, 30 s at 72 °C; 3 min at 72 °C. PCR products were purified by adding 1 U of Exonuclease I and 0.5 U FastAP Alkaline Phosphatase (Thermo Scientific, St. Leon-Rot, Germany) and incubated at 37 °C for 1 h, followed by inactivation at 80 °C for 15 min.…”
Section: Methodsmentioning
confidence: 99%
“…ITS-5.8 region of the nuclear ribosomal DNA was not sequenced because in Boletaceae, ITS commonly shows high levels of intraindividual polymorphisms for indels, thus mostly preventing straightforward phylogenetic analysis and moreover often making cloning necessary to obtain a sequence. The selected protein-coding genes have shown multiple times their usefulness for investigating phylogenetic relationships, at both infrageneric and suprageneric levels (e.g., Wu et al, 2016;Vadthanarat et al, 2019). For the amplification of atp6, ATP6-1M40F and ATP6-2M primers were used, with following the protocol and PCR program in Raspé et al (2016).…”
Section: Morphological Studiesmentioning
confidence: 99%
“…For ML, phylogenetic inference was performed using RAxML (Stamatakis, 2006) on the CIPRES web portal (RAxML-HPC2 on XSEDE; Miller et al, 2009), using the GTRCAT model with 25 categories. Three Butyriboletus species were used as outgroup based on the phylogeny in Vadthanarat et al (2019). Statistical support of clades was obtained with 1,000 rapid BS replicates.…”
Section: Alignment and Phylogeny Inferencementioning
confidence: 99%
“…& Thiers) M. Kuo & B. Ortiz are from North America [8,9]. In Asia, H. rugosum G. Wu & Zhu L. Yang is described from China, and H. indecorum (Massee) G. Wu & Zhu L. Yang is from tropical China, Singapore, Thailand [8,15,16].…”
Section: Introductionmentioning
confidence: 99%