2014
DOI: 10.1038/nbt.2899
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iGEM 2.0—refoundations for engineering biology

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Cited by 67 publications
(63 citation statements)
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“…AHL/luxR affinity was varied using the wild-type Vibrio fisheri gene and a hypersentive mutant, luxR-G2F 10 . RBS strength responsible for GFP translation was varied in the conservation of the Shine-Dalgarno sequence (BBa_B0034 and BBa_B0033 in the Registry of Standard Biological Parts 11, 12 ). Finally, GFP degradation rate was varied through the addition of the LVA-ssrA degradation tag for clpX-mediated proteolysis 13–16 .…”
Section: Resultsmentioning
confidence: 99%
“…AHL/luxR affinity was varied using the wild-type Vibrio fisheri gene and a hypersentive mutant, luxR-G2F 10 . RBS strength responsible for GFP translation was varied in the conservation of the Shine-Dalgarno sequence (BBa_B0034 and BBa_B0033 in the Registry of Standard Biological Parts 11, 12 ). Finally, GFP degradation rate was varied through the addition of the LVA-ssrA degradation tag for clpX-mediated proteolysis 13–16 .…”
Section: Resultsmentioning
confidence: 99%
“…Both the potential and limitations of standardization in SB are exemplified by the international Genetically Engineered Machine (iGEM) competition, in which students worldwide present synthetic biology projects based on organisms engineered from a toolbox of BioBricks™. However, Biobricks™ has limitations as universal building blocks in SB (Vilanova and Porcar, ; Valverde et al ., ). Interestingly, these limitations have not been an obstacle for a dense network of synthetic biology enterprises to flourish in the US, while in Europe, the landscape of synthetic biology enterprises is sparse by comparison, even if the main efforts to overcome a paucity of standardization are totally or partially of European origin, such as the development of a Standard European Vector Architecture (SEVA; Silva‐Rocha et al ., ), or the standardized representation of SB designs known as the Synthetic Biology Open Language (SBOL; Galdzicki et al ., ).…”
mentioning
confidence: 99%
“…GEC then compiles this specification to all genetic circuit designs that satisfy the specified constraints. In this example, only one design is generated because the default part database provided with GEC is relatively small and must be extended with a dual-regulatory promoter from the iGEM (Smolke 2009;Vilanova and Porcar 2014) Registry (BioBrick K094120) to obtain any solutions. To predict which design will have optimal performance, one must use GEC to compile each design to a biochemical model and simulate each model using GEC or another tool.…”
Section: Examplementioning
confidence: 99%