2019
DOI: 10.1016/j.plasmid.2019.102431
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Improving biosynthetic production of pinene through plasmid recombination elimination and pathway optimization

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Cited by 19 publications
(16 citation statements)
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“…An E. coli strain with the genes recA, recE, recF, recI and endA removed was transformed with a plasmid encoded for pinene production with strong terminators. This E. coli strain increased pinene titer by 6.9 fold [36].…”
Section: E Colimentioning
confidence: 88%
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“…An E. coli strain with the genes recA, recE, recF, recI and endA removed was transformed with a plasmid encoded for pinene production with strong terminators. This E. coli strain increased pinene titer by 6.9 fold [36].…”
Section: E Colimentioning
confidence: 88%
“…There are several challenges related to increasing E. coli-produced pinene titers. The heterologous enzymes introduced to E. coli for pinene production produce intermediates that cannot be utilized by the E. coli cell and this metabolic burden can cause plasmid instability [36]. Plasmid recombination can be reduced and pinene titer increased by altering the transcriptional rrnB-T1 terminators on the plasmid to strong terminators that are not homologous [36].…”
Section: E Colimentioning
confidence: 99%
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“…the tyre-derived oil has a significantly high concentration of DL-limonene [19,20]. On an industrial scale, a,b-pinenes are mainly obtained as byproducts of paper pulping or extracted from turpentine; new alternatives include the production of pinenes by bioprocesses using E. coli systems [21,22].…”
Section: Introductionmentioning
confidence: 99%