Finding a correct species assignment for a Metschnikowia strain: insights from the genome sequencing of strain DBT012.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Eleonora Troiano, Ilaria Larini, Renato L Binati, Veronica Gatto, Sandra Torriani, Pietro Buzzini, Benedetta Turchetti, Elisa Salvetti, Giovanna E Felis
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引用次数: 1

Abstract

Metschnikowia pulcherrima is an important yeast species that is attracting increased interest thanks to its biotechnological potential, especially in agri-food applications. Phylogenetically related species of the so-called 'pulcherrima clade' were first described and then reclassified in one single species, which makes the identification an intriguing issue. Starting from the whole-genome sequencing of the protechnological strain Metschnikowia sp. DBT012, this study applied comparative genomics to calculate similarity with the M. pulcherrima clade publicly available genomes with the aim to verify if novel single-copy putative phylogenetic markers could be selected, in comparison with the commonly used primary and secondary barcodes. The genome-based bioinformatic analysis allowed the identification of 85 consensus single-copy orthologs, which were reduced to three after split decomposition analysis. However, wet-lab amplification of these three genes in nonsequenced type strains revealed the presence of multiple copies, which made them unsuitable as phylogenetic markers. Finally, average nucleotide identity (ANI) was calculated between strain DBT012 and available genome sequences of the M. pulcherrima clade, although the genome dataset is still rather limited. Presence of multiple copies of phylogenetic markers as well as ANI values were compatible with the recent reclassification of the clade, allowing the identification of strain DBT012 as M. pulcherrima.

为Metschnikowia菌株寻找正确的物种分配:来自菌株DBT012基因组测序的见解。
pulcherrima Metschnikowia pulcherrima是一种重要的酵母品种,由于其生物技术潜力,特别是在农业食品中的应用,引起了人们越来越多的兴趣。所谓的“pulcherrima枝”的系统发育相关物种首先被描述,然后被重新分类为一个单一的物种,这使得鉴定成为一个有趣的问题。本研究从原技术菌株Metschnikowia sp. DBT012的全基因组测序开始,应用比较基因组学计算与M. pulcherrima进化支公开可用基因组的相似性,目的是验证是否可以选择新的单拷贝推定系统发育标记,并与常用的一级和二级条形码进行比较。基于基因组的生物信息学分析允许鉴定85个一致的单拷贝同源物,经过分裂分解分析后减少到3个。然而,这三个基因在非测序型菌株的湿实验室扩增显示存在多个拷贝,这使得它们不适合作为系统发育标记。最后,计算了菌株DBT012与现有M. pulcherrima分支基因组序列之间的平均核苷酸同源性(ANI),尽管基因组数据仍然相当有限。系统发育标记的多个拷贝以及ANI值的存在与该分支最近的重新分类相一致,从而使菌株DBT012被鉴定为M. pulcherrima。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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