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利用基于颜色的质粒稳定性测定法构建和表征毕赤酵母的着丝粒质粒。

Construction and characterization of centromeric plasmids for Komagataella phaffii using a color-based plasmid stability assay.

机构信息

Departamento de Biologia Celular, Bloco K, primeiro andar, Universidade de Brasília, Brasília, Brazil.

出版信息

PLoS One. 2020 Jul 2;15(7):e0235532. doi: 10.1371/journal.pone.0235532. eCollection 2020.

Abstract

The yeast Komagataella phaffii is widely used as a microbial host for heterologous protein production. However, molecular tools for this yeast are basically restricted to a few integrative and replicative plasmids. Four sequences that have recently been proposed as the K. phaffii centromeres could be used to develop a new class of mitotically stable vectors. In this work, we designed a color-based genetic assay to investigate plasmid stability in K. phaffii and constructed vectors bearing K. phaffii centromeres and the ADE3 marker. These genetic tools were evaluated in terms of mitotic stability by transforming an ade2/ade3 auxotrophic strain and regarding plasmid copy number by quantitative PCR (qPCR). Our results confirmed that the centromeric plasmids were maintained at low copy numbers as a result of typical chromosome-like segregation during cell division. These features, combined with in vivo assembly possibilities, prompt these plasmids as a new addition to the K. phaffii genetic toolbox.

摘要

毕赤酵母是一种广泛用于异源蛋白生产的微生物宿主。然而,该酵母的分子工具基本上仅限于少数几种整合型和复制型质粒。最近提出的 4 个序列可作为毕赤酵母的着丝粒,用于开发新的有丝分裂稳定载体。在这项工作中,我们设计了一种基于颜色的遗传测定法来研究毕赤酵母中的质粒稳定性,并构建了带有毕赤酵母着丝粒和 ADE3 标记的载体。通过转化 ade2/ade3 营养缺陷型菌株,并通过定量 PCR(qPCR)评估质粒拷贝数,评估了这些遗传工具的有丝分裂稳定性。我们的结果证实,由于细胞分裂过程中典型的染色体样分离,着丝粒质粒以低拷贝数维持。这些特性,结合体内组装的可能性,促使这些质粒成为毕赤酵母遗传工具包的新成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d58c/7332064/34240189c750/pone.0235532.g001.jpg

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