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首页> 外文期刊>Applied and Environmental Microbiology >Assessment of cry1 Gene Contents of Bacillus thuringiensis Strains by Use of DNA Microarrays
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Assessment of cry1 Gene Contents of Bacillus thuringiensis Strains by Use of DNA Microarrays

机译:利用DNA芯片评估苏云金芽孢杆菌菌株cry1基因的含量

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A single Bacillus thuringiensis strain can harbor numerous different insecticidal crystal protein (cry) genes from 46 known classes or primary ranks. The cry1 primary rank is the best known and contains the highest number of cry genes which currently totals over 130. We have designed an oligonucleotide-based DNA microarray (cryArray) to test the feasibility of using microarrays to identify the cry gene content of B. thuringiensis strains. Specific 50-mer oligonucleotide probes representing the cry1 primary and tertiary ranks were designed based on multiple cry gene sequence alignments. To minimize false-positive results, a consentaneous approach was adopted in which multiple probes against a specific gene must unanimously produce positive hybridization signals to confirm the presence of a particular gene. In order to validate the cryArray, several well-characterized B. thuringiensis strains including isolates from a Mexican strain collection were tested. With few exceptions, our probes performed in agreement with known or PCR-validated results. In one case, hybridization of primary- but not tertiary-ranked cry1I probes indicated the presence of a novel cry1I gene. Amplification and partial sequencing of the cry1I gene in strains IB360 and IB429 revealed the presence of a cry1Ia gene variant. Since a single microarray hybridization can replace hundreds of individual PCRs, DNA microarrays should become an excellent tool for the fast screening of new B. thuringiensis isolates presenting interesting insecticidal activity.
机译:一个苏云金芽孢杆菌菌株可以包含来自46个已知类别或主要等级的许多不同的杀虫晶体蛋白(cry)基因。 cry1主要排名是最广为人知的,它包含数量最多的cry基因,目前总数超过130。我们设计了基于寡核苷酸的DNA微阵列(cryArray),以测试使用微阵列鉴定B的cry基因含量的可行性。苏云金芽孢杆菌菌株。基于多个cry基因序列比对,设计了代表cry1第一和第三级的特异性50-mer寡核苷酸探针。为了使假阳性结果最小化,采用了一种同意的方法,其中针对特定基因的多个探针必须一致产生阳性杂交信号以确认特定基因的存在。为了验证cryArray,测试了几种特性良好的苏云金芽孢杆菌菌株,包括来自墨西哥菌株集合的分离株。除少数例外,我们的探针与已知或PCR验证的结果一致。在一种情况下,一级至第三级cry1I探针的杂交表明存在新的cry1I基因。菌株IB360和IB429中cry1I基因的扩增和部分测序表明存在cry1Ia基因变异。由于单个微阵列杂交可以代替数百个单独的PCR,因此DNA微阵列应成为快速筛选表现出令人关注的杀虫活性的新的苏云金芽孢杆菌分离株的极佳工具。

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