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由进化工程辅助的理性设计实现了恶臭假单胞菌KT2440中复杂表型的(去)构建与优化。

Rational Design Assisted by Evolutionary Engineering Allows (De)Construction and Optimization of Complex Phenotypes in Pseudomonas putida KT2440.

作者信息

Blázquez Blas, Nogales Juan

机构信息

Department of Systems Biology, Centro Nacional de Biotecnología CSIC, Madrid, Spain.

CNB DNA Biofoundry (CNBio), CSIC, Madrid, Spain.

出版信息

Microb Biotechnol. 2025 Mar;18(3):e70132. doi: 10.1111/1751-7915.70132.

DOI:10.1111/1751-7915.70132
PMID:40126873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11932161/
Abstract

Beyond the rational construction of genetic determinants to encode target functions, complex phenotype engineering requires the contextualisation of their expression within the metabolic and genetic background of the host strain. Furthermore, wherever metabolic complexity is involved, phenotype engineering demands standard, reliable, plug-and-play tools. We introduce GENIO (GENome Integration and fitness Optimization platform for Pseudomonas putida), a framework to optimise genetic circuit performance by means of (i) chromosome-location-based differential gene expression and (ii) subsequent fitness improvement through evolutionary engineering if needed. Using gene expression strength and cell-to-cell variation, we characterised 10 P. putida chromosomal loci (ppLPS) to show that genome context rather than distance to ORI is the main factor driving differential expression performance. We further contextualised ppLPS gene expression against well-known chromosomal integration sites and plasmids displaying different copy numbers. GENIO supports comprehensive exploration of the gene expression space across P. putida's genome while unlocking performance optimization of complex heterologous metabolic pathways through evolutionary engineering. To demonstrate the usability of GENIO, we restored P. putida's aromatic hydrocarbon metabolism by (de)constructing the toluene/m-xylene catabolic pathway coded in the pWW0 plasmid. We also showed that engineering complex phenotypes requires accurate contextualisation of the synthetic pathways involved, a process that benefits from biological robustness.

摘要

除了合理构建遗传决定因素以编码目标功能外,复杂的表型工程还需要在宿主菌株的代谢和遗传背景中对其表达进行情境化。此外,只要涉及代谢复杂性,表型工程就需要标准、可靠的即插即用工具。我们介绍了GENIO(恶臭假单胞菌基因组整合与适应性优化平台),这是一个通过以下方式优化遗传电路性能的框架:(i)基于染色体定位的差异基因表达,以及(ii)必要时通过进化工程提高适应性。利用基因表达强度和细胞间变异,我们对10个恶臭假单胞菌染色体位点(ppLPS)进行了表征,以表明基因组背景而非与ORI的距离是驱动差异表达性能的主要因素。我们进一步将ppLPS基因表达与显示不同拷贝数的知名染色体整合位点和质粒进行了情境化。GENIO支持全面探索恶臭假单胞菌基因组中的基因表达空间,同时通过进化工程解锁复杂异源代谢途径的性能优化。为了证明GENIO的可用性,我们通过(去)构建pWW0质粒中编码的甲苯/间二甲苯分解代谢途径,恢复了恶臭假单胞菌的芳烃代谢。我们还表明,工程化复杂表型需要对所涉及的合成途径进行准确的情境化,这一过程受益于生物稳健性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/9dfa45388400/MBT2-18-e70132-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/763ec8560716/MBT2-18-e70132-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/e75cc53c7b30/MBT2-18-e70132-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/7b9d8f6a3764/MBT2-18-e70132-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/3b55966aa001/MBT2-18-e70132-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/be75c7797185/MBT2-18-e70132-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/9dfa45388400/MBT2-18-e70132-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/763ec8560716/MBT2-18-e70132-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/e75cc53c7b30/MBT2-18-e70132-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/7b9d8f6a3764/MBT2-18-e70132-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/3b55966aa001/MBT2-18-e70132-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/be75c7797185/MBT2-18-e70132-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4eb/11932161/9dfa45388400/MBT2-18-e70132-g004.jpg

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Synthetically-primed adaptation of Pseudomonas putida to a non-native substrate D-xylose.假单胞菌属到非天然基质 D-木糖的合成启动适应性。
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The pAblo·pCasso self-curing vector toolset for unconstrained cytidine and adenine base-editing in Gram-negative bacteria.
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