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新兴宿主生物制造菌海盐单胞菌的蛋白质组学基础特征分析。

Baseline proteomics characterisation of the emerging host biomanufacturing organism Halomonas bluephagenesis.

机构信息

Manchester Institute of Biotechnology and Dept. of Chemistry, The University of Manchester, Manchester, M1 7DN, UK.

School of Life Sciences, Tsinghua University, 100084, Beijing, China.

出版信息

Sci Data. 2022 Aug 13;9(1):492. doi: 10.1038/s41597-022-01610-0.

Abstract

Despite its greener credentials, biomanufacturing remains financially uncompetitive compared with the higher carbon emitting, hydrocarbon-based chemical industry. Replacing traditional chassis such as E. coli with novel robust organisms, are a route to cost reduction for biomanufacturing. Extremophile bacteria such as the halophilic Halomonas bluephagenesis TD01 exemplify this potential by thriving in environments inherently inimical to other organisms, so reducing sterilisation costs. Novel chassis are inevitably less well annotated than established organisms. Rapid characterisation along with community data sharing will facilitate adoption of such organisms for biomanufacturing. The data record comprises a newly sequenced genome for the organism and evidence via LC-MS based proteomics for expression of 1160 proteins (30% of the proteome) including baseline quantification of 1063 proteins (27% of the proteome), and a spectral library enabling re-use for targeted LC-MS proteomics assays. Protein data are annotated with KEGG Orthology, enabling rapid matching of quantitative data to pathways of interest to biomanufacturing.

摘要

尽管生物制造具有更环保的特点,但与碳排放更高的碳氢化合物化学工业相比,其在财务上仍不具备竞争力。用新型的、强健的生物体替代传统的底盘,例如大肠杆菌,是降低生物制造成本的一种途径。嗜盐菌 Halomonas bluephagenesis TD01 等极端微生物就是这种潜力的典范,它们在对其他生物体有害的环境中茁壮成长,从而降低了消毒成本。新型底盘的注释必然不如已建立的生物体详细。快速的特征描述以及社区数据共享将有助于采用这些生物体进行生物制造。该数据记录包含该生物体的新测序基因组以及通过基于 LC-MS 的蛋白质组学表达 1160 种蛋白质(占蛋白质组的 30%)的证据,包括 1063 种蛋白质(占蛋白质组的 27%)的基线定量,以及一个可用于针对 LC-MS 蛋白质组学测定进行重新使用的光谱库。蛋白质数据被注释为 KEGG Orthology,使定量数据能够快速与生物制造感兴趣的途径相匹配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21fd/9376085/c398aa78a740/41597_2022_1610_Fig1_HTML.jpg

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