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The analysis of T-DNA insertional Colletotrichum gloeosporioides in Stylo pathogenicity-weakened mutant strain 1681

机译:T-DNA插入Colletottrichum GloooSporioids的分析致力致病性弱化突变菌株1681

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Biological phenotypes of mutant strain 1681 that was the pathogenicity-reduced strain in Colletotrichum gloeosporioides of Stylosanthes guianensia were analyzed by testing growth rate, colonial morphologies and sporulation ability. TAIL-PCR was used to identify the T-DNA integration site and the genes of flanking right site of the T-DNA. The sequences was analyzed by local blast and the gene and the function were predicted by bioinformatics methods. The results showed that the pathogenicity of the mutant 1681 was reduced by comparing with wild type strain CH008 in Colletotrichum gloeosporioides of Stylosanthes guianensis. The growth rate between strain 1681(1.42±0.02)cm/d and CH008(1.41±0.03)cm/d had no significant difference. The sporulation between strain 1681(1.50±0.25)×10~6/mL and CH008(9.26±0.14)×10~6/mL had significant difference. The spore germination rate between strain 1681(0.00±0.00)% and CH008(91.14±6.66)% had significant difference. In contrast the colony diameter and colony morphology had no significant difference. Two sequences were cloned by TAIL-PCR. The length of the RB flanking sequence was 412 bp and the LB flanking sequence was 381 bp. The blast result showed that the sequence had 100% homology to genome of wild type strain CH008 in Colletotrichum gloeosporioides of Stylosanthes guianensis. The bioinformatics analysis showed the T-DNA maker the area of initial exon. It contains a complete open reading frame (ORF), encoding 682 amino acid. By predicting the function of sequence in NCBI, the blast result showed that the sequence had 99% homology to gene Nara gc5 phenylalanyl-tRNA synthetase (PheRS) beta chain core domain. It belongs to the class II aminoacyl-tRNA synthetases (aaRS) like-core super family based upon its structure.
机译:通过试验生长速率,殖民形态和孢子化能力,分析了突变菌株1681的生物学表型,即令人血吸虫的诱导仪Guianensia的致病性降低菌株。尾PCR用于鉴定T-DNA集成位点和T-DNA的侧翼右位的基因。通过局部爆炸和基因分析序列,并通过生物信息学方法预测该功能。结果表明,通过与令人抑制仪诱导仪的甲状腺孢子孢子孢子孢子孢子孢子孢子孢子虫的野生型菌株CH008比较,减少了突变体1681的致病性。菌株1681(1.42±0.02)CM / D和CH008(1.41±0.03)CM / D之间的生长速率没有显着差异。菌株1681(1.50±0.25)×10〜6 / ml和CH008(9.26±0.14)×10〜6 / ml之间的孢子率具有显着差异。菌株1681(0.00±0.00)%和CH008(91.14±6.66)%之间的孢子萌发率具有显着差异。相比之下,菌落直径和菌落形态没有显着差异。尾PCR克隆了两个序列。 RB侧翼序列的长度为412bp,Lb侧翼序列为381bp。 BLAST结果表明,该序列对令人突如其氏菌氏菌菌的Collettrichum Guiancorioides的野生型菌株CH008基因组100%同源性。生物信息学分析显示T-DNA制造商初始外显子面积。它包含一个完整的开放阅读框(ORF),编码682个氨基酸。通过预测NCBI中序列的函数,BLAST结果表明,该序列与基因NARA GC5苯丙基-TRNA合成酶(PHEERS)β链核心结构域具有99%同源性。它属于II类氨基酰基-TRNA合成酶(AARS)类似核心超级家族的基础结构。

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