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Comparative genomics of citric-acid-producing Aspergillus niger ATCC 1015 versus enzyme-producing CBS 513.88

机译:产柠檬酸的黑曲霉aTCC 1015与产酶CBs的比较基因组学513.88

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摘要

The filamentous fungus Aspergillus niger exhibits great diversity in its phenotype. It is found globally, both as marine and terrestrial strains, produces both organic acids and hydrolytic enzymes in high amounts, and some isolates exhibit pathogenicity. Although the genome of an industrial enzyme-producing A. niger strain (CBS 513.88) has already been sequenced, the versatility and diversity of this species compel additional exploration. We therefore undertook whole-genome sequencing of the acidogenic A. niger wild-type strain (ATCC 1015) and produced a genome sequence of very high quality. Only 15 gaps are present in the sequence, and half the telomeric regions have been elucidated. Moreover, sequence information from ATCC 1015 was used to improve the genome sequence of CBS 513.88. Chromosome-level comparisons uncovered several genome rearrangements, deletions, a clear case of strain-specific horizontal gene transfer, and identification of 0.8 Mb of novel sequence. Single nucleotide polymorphisms per kilobase (SNPs/kb) between the two strains were found to be exceptionally high (average: 7.8, maximum: 160 SNPs/kb). High variation within the species was confirmed with exo-metabolite profiling and phylogenetics. Detailed lists of alleles were generated, and genotypic differences were observed to accumulate in metabolic pathways essential to acid production and protein synthesis. A transcriptome analysis supported up-regulation of genes associated with biosynthesis of amino acids that are abundant in glucoamylase A, tRNA-synthases, and protein transporters in the protein producing CBS 513.88 strain. Our results and data sets from this integrative systems biology analysis resulted in a snapshot of fungal evolution and will support further optimization of cell factories based on filamentous fungi.
机译:丝状真菌黑曲霉在其表型上表现出极大的多样性。它在全球范围内都被发现,既可以作为海洋菌株也可以作为陆地菌株,同时产生大量的有机酸和水解酶,并且某些分离株具有致病性。尽管已经对产酶的工业黑曲霉菌株(CBS 513.88)的基因组进行了测序,但该物种的多功能性和多样性迫使人们进行了进一步的探索。因此,我们对产酸黑曲霉野生型菌株(ATCC 1015)进行了全基因组测序,并产生了高质量的基因组序列。该序列中仅存在15个缺口,并且已经阐明了一半的端粒区域。此外,来自ATCC 1015的序列信息被用于改善CBS 513.88的基因组序列。染色体水平的比较发现了一些基因组重排,缺失,菌株特异性水平基因转移的明确案例以及0.8 Mb的新序列的鉴定。发现两个菌株之间每千碱基的单核苷酸多态性(SNPs / kb)非常高(平均:7.8,最大:160 SNPs / kb)。通过外代谢物分析和系统发育学证实了该物种内的高度变异。产生了等位基因的详细列表,并观察到基因型差异在酸产生和蛋白质合成必不可少的代谢途径中积累。转录组分析支持与蛋白质合成CBS 513.88菌株中糖淀粉酶A,tRNA合酶和蛋白质转运蛋白中丰富的氨基酸的生物合成相关的基因的上调。我们从该综合系统生物学分析中获得的结果和数据集可提供真菌进化的快照,并将支持基于丝状真菌的细胞工厂的进一步优化。

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