Polaris: A toolkit for standardized construction, integration, and quantitative testing in Escherichia coli and Saccharomyces cerevisiae
面向大肠杆菌和酿酒酵母标准化构建、基因组整合与定量测试的工具包
摘要
Existing synthetic biology toolkits have expanded part libraries and assembly capabilities. However, new users may still encounter ambiguity in construct definitions, hierarchical transitions, genomic integration routes, and quantitative testing procedures. Here, we present Polaris, a Golden Gate toolkit for Escherichia coli and Saccharomyces cerevisiae. Polaris defines a shared three-level hierarchy. Level 1 stores reusable parts, Level 2 generates transcription units and other intermediate constructs, and Level 3 supports multigene assembly and switching between testing and integration backbones. The toolkit distinguishes part interfaces from transcription unit interfaces, uses BpiI and BsaI in successive assembly stages, and provides parallel ccdB and mScarletI3 screening options. Integration modules and quantitative characterization frameworks were implemented in both hosts and demonstrated using representative genetic parts and activation and repression systems. A companion digital platform further encodes the Level 1 to Level 3 rules for assembly planning. Polaris connects hierarchical construction, stable genetic implementation, and quantitative testing within a common execution framework, providing a practical basis for data accumulation, part standardization, and future automation.
参考文献
[1] Engler C, Kandzia R, Marillonnet S. A one pot, one step, precision cloning method with high throughput capability. PLoS One 2008;3:e3647. https://doi.org/10.1371/journal.pone.0003647.
[2] Weber E, Engler C, Gruetzner R, Werner S, Marillonnet S. A modular cloning system for standardized assembly of multigene constructs. PLoS One 2011;6:e16765. https://doi.org/10.1371/journal.pone.0016765.
[3] Lee ME, DeLoache WC, Cervantes B, Dueber JE. A highly characterized yeast toolkit for modular, multipart assembly. ACS Synth Biol 2015;4:975-86. https://doi.org/10.1021/sb500366v.
[4] Iverson SV, Haddock TL, Beal J, Densmore DM. CIDAR MoClo: improved MoClo assembly standard and new E. coli part library enable rapid combinatorial design for synthetic and traditional biology. ACS Synth Biol 2016;5:99-103. https://doi.org/10.1021/acssynbio.5b00124.
[5] Moore SJ, Lai HE, Kelwick RJR, Chee SM, Bell DJ, Polizzi KM, et al. EcoFlex: a multifunctional MoClo kit for E. coli synthetic biology. ACS Synth Biol 2016;5:1059-69. https://doi.org/10.1021/acssynbio.6b00031.
[6] Blázquez B, San León D, Torres-Bacete J, Gómez-Luengo A, Kniewel R, Martínez I, et al. Golden Standard: a complete standard, portable, and interoperative MoClo tool for model and non-model proteobacteria. Nucleic Acids Res 2023;51:e98. https://doi.org/10.1093/nar/gkad758.
[7] Mejlsted J, Kubaczka E, Wirth S, Koeppl H. The Coli Toolkit (CTK): an extension of the modular yeast toolkit for use in E. coli. ACS Synth Biol 2026;15:462-71. https://doi.org/10.1021/acssynbio.5c00489.
[8] Nielsen AAK, Der BS, Shin J, Vaidyanathan P, Paralanov V, Strychalski EA, et al. Genetic circuit design automation. Science 2016;352:aac7341. https://doi.org/10.1126/science.aac7341.
[9] Chen Y, Zhang S, Young EM, Jones TS, Densmore D, Voigt CA. Genetic circuit design automation for yeast. Nat Microbiol 2020;5:1349-60. https://doi.org/10.1038/s41564-020-0757-2.
[10] Ham TS, Dmytriv Z, Plahar H, Chen J, Hillson NJ, Keasling JD. Design, implementation and practice of JBEI-ICE: an open source biological part registry platform and tools. Nucleic Acids Res 2012;40:e141. https://doi.org/10.1093/nar/gks531.
[11] McLaughlin JA, Beal J, Mısırlı G, Grünberg R, Bartley BA, Scott-Brown J, et al. The Synthetic Biology Open Language (SBOL) version 3: simplified data exchange for bioengineering. Front Bioeng Biotechnol 2020;8:1009. https://doi.org/10.3389/fbioe.2020.01009.
[12] Kelly JR, Rubin AJ, Davis JH, Ajo-Franklin CM, Cumbers J, Czar MJ, et al. Measuring the activity of BioBrick promoters using an in vivo reference standard. J Biol Eng 2009;3:4. https://doi.org/10.1186/1754-1611-3-4.
[13] Mutalik VK, Guimaraes JC, Cambray G, Lam C, Christoffersen MJ, Mai QA, et al. Precise and reliable gene expression via standard transcription and translation initiation elements. Nat Methods 2013;10:354-60. https://doi.org/10.1038/nmeth.2404.
[14] Chen YJ, Liu P, Nielsen AAK, Brophy JAN, Clancy K, Peterson T, et al. Characterization of 582 natural and synthetic terminators and quantification of their design constraints. Nat Methods 2013;10:659-64. https://doi.org/10.1038/nmeth.2515.
[15] Cardinale S, Arkin AP. Contextualizing context for synthetic biology - identifying causes of failure of synthetic biological systems. Biotechnol J 2012;7:856-66. https://doi.org/10.1002/biot.201200085.
[16] Lou C, Stanton B, Chen YJ, Munsky B, Voigt CA. Ribozyme-based insulator parts buffer synthetic circuits from genetic context. Nat Biotechnol 2012;30:1137-42. https://doi.org/10.1038/nbt.2401.
[17] Bayer CN, Rennig M, Ehrmann AK, Nørholm MHH. A standardized genome architecture for bacterial synthetic biology (SEGA). Nat Commun 2021;12:5876. https://doi.org/10.1038/s41467-021-26155-5.
[18] Lux MW, Strychalski EA, Vora GJ. Advancing reproducibility can ease the ‘hard truths’ of synthetic biology. Synth Biol (Oxf) 2023;8:ysad014. https://doi.org/10.1093/synbio/ysad014.
[19] Lund BA, Leiros HKS, Bjerga GK. A high-throughput, restriction-free cloning and screening strategy based on ccdB-gene replacement. Microb Cell Fact 2014;13:38. https://doi.org/10.1186/1475-2859-13-38.
[20] Wang H, Bian X, Xia L, Ding X, Müller R, Zhang Y, et al. Improved seamless mutagenesis by recombineering using ccdB for counterselection. Nucleic Acids Res 2014;42:e37. https://doi.org/10.1093/nar/gkt1339.
[21] Zhang X, Teng C, Lyu K, Lyu S, Fan Y. ‘Two in One’ cloning vector applied for blunt-end and T-A cloning with one-step digestion-ligation and screening of positive recombinants by unaided eyes. Curr Issues Mol Biol 2025;47:17. https://doi.org/10.3390/cimb47010017.
[22] Meyer AJ, Segall-Shapiro TH, Glassey E, Zhang J, Voigt CA. Escherichia coli “Marionette” strains with 12 highly optimized small-molecule sensors. Nat Chem Biol 2019;15:196-204. https://doi.org/10.1038/s41589-018-0168-3.
[23] Wang T, Xie R, Ma Z, Chen Y. A unified computational framework for quantitative design and optimization of transcriptional regulation across bacterial species. Nucleic Acids Res 2026;54:gkaf1472. https://doi.org/10.1093/nar/gkaf1472.
[24] Tafoya-Ramírez M, Padilla-Vaca F, Ramírez-Saldaña A, Mora-Garduño J, Rangel-Serrano A, Vargas-Maya N, et al. Replacing standard reporters from molecular cloning plasmids with chromoproteins for positive clone selection. Molecules 2018;23:1328. https://doi.org/10.3390/molecules23061328.
[25] Wu P, Li X, Yang M, Huang Z, Mo H, Li T, et al. High-throughput, one-step screening, cloning and expression based on the lethality of DpnI in Escherichia coli. Biochem Biophys Res Commun 2018;504:177-83. https://doi.org/10.1016/j.bbrc.2018.08.151.
[26] Park Y, Espah Borujeni A, Gorochowski TE, Shin J, Voigt CA. Precision design of stable genetic circuits carried in highly-insulated E. coli genomic landing pads. Mol Syst Biol 2020;16:e9584. https://doi.org/10.15252/msb.20209584.
[27] Yang L, Nielsen AAK, Fernandez-Rodriguez J, McClune CJ, Laub MT, Lu TK, et al. Permanent genetic memory with >1-byte capacity. Nat Methods 2014;11:1261-6. https://doi.org/10.1038/nmeth.3147.
[28] Landy A. Dynamic, structural, and regulatory aspects of λ site-specific recombination. Annu Rev Biochem 1989;58:913-41. https://doi.org/10.1146/annurev.bi.58.070189.004405.
[29] Li Q, Sun B, Chen J, Zhang Y, Jiang Y, Yang S. A modified pCas/pTargetF system for CRISPR-Cas9-assisted genome editing in Escherichia coli. Acta Biochim Biophys Sin (Shanghai) 2021;53:620-7. https://doi.org/10.1093/abbs/gmab036.
[30] Reider Apel A, d'Espaux L, Wehrs M, Sachs D, Li RA, Tong GJ, et al. A Cas9-based toolkit to program gene expression in Saccharomyces cerevisiae. Nucleic Acids Res 2017;45:496-508. https://doi.org/10.1093/nar/gkw1023.
[31] Meng J, Qiu Y, Zhang Y, Zhao H, Shi S. CMI: CRISPR/Cas9 based efficient multiplexed integration in Saccharomyces cerevisiae. ACS Synth Biol 2023;12:1408-14. https://doi.org/10.1021/acssynbio.2c00591.
[32] Goldstein AL, Pan X, McCusker JH. Heterologous URA3MX cassettes for gene replacement in Saccharomyces cerevisiae. Yeast 1999;15:507-11. https://doi.org/10.1002/(SICI)1097-0061(199904)15:6<507::AID-YEA369>3.0.CO;2-P.
[33] Gueldener U, Heinisch J, Koehler GJ, Voss D, Hegemann JH. A second set of loxP marker cassettes for Cre-mediated multiple gene knockouts in budding yeast. Nucleic Acids Res 2002;30:e23. https://doi.org/10.1093/nar/30.6.e23.
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