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Molecular Diagnostic for Prospecting Polyhydroxyalkanoate-Producing Bacteria

机译:产多羟基链烷酸细菌的分子诊断

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摘要

The use of molecular diagnostic techniques for bioprospecting and microbial diversity study purposes has gained more attention thanks to their functionality, low cost and quick results. In this context, ten degenerate primers were designed for the amplification of polyhydroxyalkanoate synthase (phaC) gene, which is involved in the production of polyhydroxyalkanoate (PHA)—a biodegradable, renewable biopolymer. Primers were designed based on multiple alignments of phaC gene sequences from 218 species that have their genomes already analyzed and deposited at Biocyc databank. The combination of oligos phaCF3/phaCR1 allowed the amplification of the expected product (PHA synthases families types I and IV) from reference organisms used as positive control (PHA producer). The method was also tested in a multiplex system with two combinations of initiators, using 16 colonies of marine bacteria (pre-characterized for PHA production) as a DNA template. All amplicon positive organisms (n = 9) were also PHA producers, thus no false positives were observed. Amplified DNA was sequenced (n = 4), allowing for the confirmation of the phaC gene identity as well its diversity among marine bacteria. Primers were also tested for screening purposes using 37 colonies from six different environments. Almost 30% of the organisms presented the target amplicon. Thus, the proposed primers are an efficient tool for screening bacteria with potential for the production of PHA as well to study PHA genetic diversity.
机译:由于分子诊断技术的功能,低成本和快速的结果,将其用于生物勘探和微生物多样性研究的目的得到了越来越多的关注。在这种情况下,设计了十个简并引物来扩增聚羟基链烷酸酯合酶(phaC)基因,该基因参与了聚羟基链烷酸酯(PHA)(一种可生物降解的可再生生物聚合物)的生产。引物是根据来自218个物种的phaC基因序列的多重比对设计的,这些物种的基因组已经被分析并保存在Biocyc数据库中。寡核苷酸phaCF3 / phaCR1的组合可从用作阳性对照(PHA生产者)的参考生物中扩增出预期的产物(I和IV型PHA合成酶家族)。还使用16种海洋细菌菌落(已预先表征用于生产PHA)作为DNA模板,在具有两种引发剂组合的多重系统中测试了该方法。所有扩增子阳性生物(n = 9)也是PHA生产者,因此未观察到假阳性。对扩增的DNA进行测序(n = 4),从而可以确认phaC基因的同一性及其在海洋细菌中的多样性。还使用来自六个不同环境的37个菌落测试了引物的筛选目的。几乎30%的生物体均显示了目标扩增子。因此,所提出的引物是用于筛选具有生产PHA潜能的细菌以及研究PHA遗传多样性的有效工具。

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