2017
DOI: 10.5943/sif/2/1/4
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The molecular phylogeny and taxonomy of endophytic fungal species from the leaves of Vitex negundo L.

Abstract: Enormous fungal species live within the healthy plant tissues, some of which presumably occur in a symbiotic association with host. Some fungal endophytes are widespread and can be found in many different plant species, whereas others are highly specific to single hosts. In this study, we isolated three endophytic fungi from the medicinal plant Vitex negundo. They were identified based on morphological characteristics such as size, shape, and colour of the spore and it was reinforced by 18s rRNA gene sequence … Show more

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Cited by 7 publications
(3 citation statements)
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“…These endophytes were identi ed using ITS region of rDNA as P. funiculosum, C. lacerate and E. endophytica. The ITS region of rDNA sequences is widely used to examine phylogenetic positions or relationship of a species because this region are anked by preserved segments (18S, 5.8S and 28S genes) which provide information about the phylogeny and the taxonomic level, since their evolution is slow and they are highly similar within different taxa (Ramesh et al, 2017).…”
Section: Discussionmentioning
confidence: 99%
“…These endophytes were identi ed using ITS region of rDNA as P. funiculosum, C. lacerate and E. endophytica. The ITS region of rDNA sequences is widely used to examine phylogenetic positions or relationship of a species because this region are anked by preserved segments (18S, 5.8S and 28S genes) which provide information about the phylogeny and the taxonomic level, since their evolution is slow and they are highly similar within different taxa (Ramesh et al, 2017).…”
Section: Discussionmentioning
confidence: 99%
“…lacerate and E. endophytica. The ITS region of rDNA sequences is widely used to examine phylogenetic positions or relationship of a species because this region are flanked by preserved segments (18S, 5.8S and 28S genes) which provide information about the phylogeny and the taxonomic level, since their evolution is slow and they are highly similar within different taxa (Ramesh et al, 2017).…”
Section: Discussionmentioning
confidence: 99%
“…PCR amplification of the fungal rDNA internal transcribed spacers (ITS) regions of all the isolates were done using the primer pairs ITS1 and ITS4. PCR amplifications conditions included 1 cycle of 94 °C for 3 min, followed by 35 cycles of 94 °C for 30 sec, 55 °C for 1 min, and 72 °C for 1 min and a final extension cycle of 72 °C for 10 min (Ramesh et al 2017). The PCR products were checked for quality using gel electrophoresis.…”
Section: Molecular Characterizationmentioning
confidence: 99%