Synthetic Biology最新文献

Utilizing a Cell-free Protein Synthesis Platform for the Biosynthesis of a Natural Product, Caffeine 利用无细胞蛋白质合成平台生物合成天然产品咖啡因

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2023-12-22 DOI: 10.1093/synbio/ysad017

Alexander Ditzel, Fanglong Zhao, Xue Gao, George N Phillips

引用次数: 0

Advancing reproducibility can ease the ‘hard truths’ of synthetic biology 提高可重复性可以缓解合成生物学的“残酷事实”

4区生物学

Synthetic Biology Pub Date : 2023-01-01 DOI: 10.1093/synbio/ysad014

Matthew W Lux, Elizabeth A Strychalski, Gary J Vora

引用次数: 0

Efficient and iterative retron-mediated in vivo recombineering in Escherichia coli 高效迭代逆转录介导的大肠杆菌体内重组

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2022-05-03 DOI: 10.1093/synbio/ysac007

A. Ellington, Christopher R. Reisch

{"title":"Efficient and iterative retron-mediated in vivo recombineering in Escherichia coli","authors":"A. Ellington, Christopher R. Reisch","doi":"10.1093/synbio/ysac007","DOIUrl":"https://doi.org/10.1093/synbio/ysac007","url":null,"abstract":"Abstract Recombineering is an important tool in gene editing, enabling fast, precise and highly specific in vivo modification of microbial genomes. Oligonucleotide-mediated recombineering via the in vivo production of single-stranded DNA can overcome the limitations of traditional recombineering methods that rely on the exogenous delivery of editing templates. By modifying a previously reported plasmid-based system for fully in vivo single-stranded DNA recombineering, we demonstrate iterative editing of independent loci by utilizing a temperature-sensitive origin of replication for easy curing of the editing plasmid from recombinant cells. Optimization of the promoters driving the expression of the system’s functional components, combined with targeted counterselection against unedited cells with Cas9 nuclease, enabled editing efficiencies of 90–100%. The addition of a dominant-negative mutL allele to the system allowed single-nucleotide edits that were otherwise unachievable due to mismatch repair. Finally, we tested alternative recombinases and found that efficiency significantly increased for some targets. Requiring only a single cloning step for retargeting, our system provides an easy-to-use method for rapid, efficient construction of desired mutants. Graphical Abstract","PeriodicalId":22158,"journal":{"name":"Synthetic Biology","volume":"23 1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2022-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74123254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 2

Xer recombination for the automatic deletion of selectable marker genes from plasmids in enteric bacteria 肠道细菌质粒中选择性标记基因自动缺失的Xer重组

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2022-04-13 DOI: 10.1093/synbio/ysac005

P. Salerno, Matthew W. Leckenby, Bruce Humphrey, Rocky M. Cranenburgh

{"title":"Xer recombination for the automatic deletion of selectable marker genes from plasmids in enteric bacteria","authors":"P. Salerno, Matthew W. Leckenby, Bruce Humphrey, Rocky M. Cranenburgh","doi":"10.1093/synbio/ysac005","DOIUrl":"https://doi.org/10.1093/synbio/ysac005","url":null,"abstract":"Abstract Antibiotic resistance genes are widely used to select bacteria transformed with plasmids and to prevent plasmid loss from cultures, yet antibiotics represent contaminants in the biopharmaceutical manufacturing process, and retaining antibiotic resistance genes in vaccines and biological therapies is discouraged by regulatory agencies. To overcome these limitations, we have developed X-mark™, a novel technology that leverages Xer recombination to generate selectable marker gene-free plasmids for downstream therapeutic applications. Using this technique, X-mark plasmids with antibiotic resistance genes flanked by XerC/D target sites are generated in Escherichia coli cytosol aminopeptidase (E. coli pepA) mutants, which are deficient in Xer recombination on plasmids, and subsequently transformed into enteric bacteria with a functional Xer system. This results in rapid deletion of the resistance gene at high resolution (100%) and stable replication of resolved plasmids for more than 40 generations in the absence of antibiotic selective pressure. This technology is effective in both Escherichia coli and Salmonella enterica bacteria due to the high degree of homology between accessory sequences, including strains that have been developed as oral vaccines for clinical use. X-mark effectively eliminates any regulatory and safety concerns around antibiotic resistance carryover in biopharmaceutical products, such as vaccines and therapeutic proteins. Graphical Abstract","PeriodicalId":22158,"journal":{"name":"Synthetic Biology","volume":"24 1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2022-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91366580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Development of synthetic biotics as treatment for human diseases 合成生物制剂治疗人类疾病的发展

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2022-01-31 DOI: 10.1093/synbio/ysac001

A. Brennan

引用次数: 9

Generation and Application of a Versatile CRISPR Toolkit for Mammalian Cell Engineering 哺乳动物细胞工程中多功能CRISPR工具箱的生成和应用

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2021-11-12 DOI: 10.1093/synbio/ysab033

N. Dang, Alissa Lance-Byrne, Angela Tung, Xiaoge Guo, Ryan J. Cecchi, Joanna Buchthal, Alejandro Chavez, N. C. Yeo

{"title":"Generation and Application of a Versatile CRISPR Toolkit for Mammalian Cell Engineering","authors":"N. Dang, Alissa Lance-Byrne, Angela Tung, Xiaoge Guo, Ryan J. Cecchi, Joanna Buchthal, Alejandro Chavez, N. C. Yeo","doi":"10.1093/synbio/ysab033","DOIUrl":"https://doi.org/10.1093/synbio/ysab033","url":null,"abstract":"\u0000 CRISPR/Cas9 has revolutionized the field of genome engineering. Yet, as the CRISPR toolbox has rapidly expanded, there remains a need for a comprehensive library of CRISPR/Cas9 reagents that allow users to perform complex cellular and genetic manipulations without requiring labor-intensive generation of reagents to meet each user’s unique experimental circumstances. Here we described the creation and validation of a pNAX CRISPR library consisting of 72 different Cas9 and gRNA expression plasmids to allow for efficient multiplex gene editing, activation, and repression in mammalian cells. The toolkit plasmids, which are piggyBac or lentiviral based, provide the means for reliable and rapid delivery of Cas9/gRNA through either transient transfection or stable integration. Using the toolkit, we demonstrate the ease with which users can perform single or multiplex gene editing and modulate the expression of both coding and non-coding genes. We also highlight the use of the comprehensive toolkit to perform combinatorial gene knockout to identify factors that regulate homologous recombination, along with investigating the regulatory role of a 68-kb intronic region associated with human disease.","PeriodicalId":22158,"journal":{"name":"Synthetic Biology","volume":"1 1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83629927","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

A linear programming-based strategy to save pipette tips in automated DNA assembly 一种基于线性规划的策略来保存自动DNA组装中的移液器尖端

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2021-10-15 DOI: 10.1093/synbio/ysac004

Kirill Sechkar, Z. Tuza, G. Stan

{"title":"A linear programming-based strategy to save pipette tips in automated DNA assembly","authors":"Kirill Sechkar, Z. Tuza, G. Stan","doi":"10.1093/synbio/ysac004","DOIUrl":"https://doi.org/10.1093/synbio/ysac004","url":null,"abstract":"Laboratory automation and mathematical optimisation are key to improving the efficiency of synthetic biology research. While there are algorithms optimising the construct designs and synthesis strategies for DNA assembly, the optimisation of how DNA assembly reaction mixes are prepared remains largely unexplored. Here, we focus on reducing the pipette tip consumption of a liquid-handling robot as it delivers DNA parts across a multi-well plate where several constructs are being assembled in parallel. We propose a linear programming formulation of this problem based on the capacitated vehicle routing problem, along with an algorithm which applies a linear programming solver to our formulation, hence providing a strategy to prepare a given set of DNA assembly mixes using fewer pipette tips. The algorithm performed well in randomly generated and real-life scenarios concerning several modular DNA assembly standards, proving capable of reducing the pipette tip consumption by up to 61% in large-scale cases. Combining automatic process optimisation and robotic liquid-handling, our strategy promises to greatly improve the efficiency of DNA assembly, either used alone or in combination with other algorithmic methods.","PeriodicalId":22158,"journal":{"name":"Synthetic Biology","volume":"51 1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84976747","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 3

SynBiopython: an open-source software library for Synthetic Biology SynBiopython:合成生物学的开源软件库

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2021-01-01 DOI: 10.1093/synbio/ysab001

Jing Wui Yeoh, Neil Swainston, Peter Vegh, Valentin Zulkower, Pablo Carbonell, M. B. Holowko, Gopal Peddinti, C. Poh

引用次数: 7

Standardization of inducer-activated broad host range expression modules: debugging and refactoring an alkane-responsive AlkS/PalkB device 诱导剂激活的宽宿主范围表达模块的标准化:烷烃响应AlkS/PalkB设备的调试和重构

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2020-12-26 DOI: 10.1093/synbio/ysab030

Alejandro Arce-Rodríguez, Ilaria Benedetti, Rafael Silva-Rocha, V. de Lorenzo

{"title":"Standardization of inducer-activated broad host range expression modules: debugging and refactoring an alkane-responsive AlkS/PalkB device","authors":"Alejandro Arce-Rodríguez, Ilaria Benedetti, Rafael Silva-Rocha, V. de Lorenzo","doi":"10.1093/synbio/ysab030","DOIUrl":"https://doi.org/10.1093/synbio/ysab030","url":null,"abstract":"Although inducible heterologous expression systems have been available since the birth of recombinant DNA technology, the diversity of devices and genetic architectures of the corresponding vectors have often resulted in a lack of reproducibility and interoperability. In an effort to increase predictability of expression of genes of interest in a variety of possible bacterial hosts we propose a composition standard for debugging and reassembling all regulatory parts that participate in the performance of such devices. As a case study we address the n-octane and dicyclopropyl ketone (DCPK)-inducible PalkB promoter of the alkane biodegradation pOCT plasmid of Pseudomonas putida. The standardized expression module consisted of an edited alkS regulatory gene that is divergently expressed and separated of PalkB by a synthetic DNA buffer sequence. The native DNA sequence of the structural alkS gene was modified to alleviate the catabolite repression exerted by some carbon and nitrogen sources through the Crc/Hfq complex of some hosts. The PalkB promoter along with the alkS variants were then formatted as SEVA (Standard European Vector Architecture) cargoes and their activity parameters in P. putida determined with GFP and luminiscent reporters. The thereby refactored system showed improvements in various features desirable in conditional expression modules: inducibility, capacity, noise reduction and on/off ratio. When applied to other promoter/regulator pairs, the compositional standard thereby implemented in the AlkS/PalkB module will enable more complex genetic programming in non-model bacteria.","PeriodicalId":22158,"journal":{"name":"Synthetic Biology","volume":"18 1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2020-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85708124","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 2

A broad-host-range event detector: expanding and quantifying performance between Escherichia coli and Pseudomonas species 广泛宿主范围事件检测器:大肠杆菌和假单胞菌之间的扩展和量化性能

IF 3.2 4区生物学

Synthetic Biology Pub Date : 2020-01-01 DOI: 10.1093/synbio/ysaa002

Nymul E. Khan, Enoch Yeung, Yuliya Farris, S. Fansler, Hans C. Bernstein

{"title":"A broad-host-range event detector: expanding and quantifying performance between Escherichia coli and Pseudomonas species","authors":"Nymul E. Khan, Enoch Yeung, Yuliya Farris, S. Fansler, Hans C. Bernstein","doi":"10.1093/synbio/ysaa002","DOIUrl":"https://doi.org/10.1093/synbio/ysaa002","url":null,"abstract":"Modern microbial biodesign relies on the principle that well-characterized genetic parts can be reused and reconfigured for different functions. However, this paradigm has only been successful in a limited set of hosts, mostly comprised from common lab strains of Escherichia coli. It is clear that new applications such as chemical sensing and event logging in complex environments will benefit from new host chassis. This study quantitatively compared how the same chemical event logger performed across four strains and three different microbial species. An integrase-based sensor and memory device was operated by two representative soil Pseudomonads—Pseudomonas fluorescens SBW25 and Pseudomonas putida DSM 291. Quantitative comparisons were made between these two non-traditional hosts and two benchmark E. coli chassis including the probiotic Nissle 1917 and common cloning strain DH5α. The performance of sensor and memory components changed according to each host, such that a clear chassis effect was observed and quantified. These results were obtained via fluorescence from reporter proteins that were transcriptionally fused to the integrase and downstream recombinant region and via data-driven kinetic models. The Pseudomonads proved to be acceptable chassis for the operation of this event logger, which outperformed the common E. coli DH5α in many ways. This study advances an emerging frontier in synthetic biology that aims to build broad-host-range devices and understand the context by which different species can execute programmable genetic operations.","PeriodicalId":22158,"journal":{"name":"Synthetic Biology","volume":"24 1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85385553","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 9