The genetic, physiological and metabolic diversity of microalgae has driven fundamental research into photosynthesis, flagella structure and function, and eukaryotic evolution. Within the last 10 years these organisms have also been investigated as potential biotechnology platforms, for example to produce high value compounds such as long chain polyunsaturated fatty acids, pigments and antioxidants, and for biodiesel precursors, in particular triacylglycerols (TAGs). Transformation protocols, molecular tools and genome sequences are available for a number of model species including the green alga Chlamydomonas reinhardtii and the diatom Phaeodactylum tricornutum, although for both species there are bottlenecks to be overcome to allow rapid and predictable genetic manipulation. One approach to do this would be to apply the principles of synthetic biology to microalgae, namely the cycle of Design-Build-Test, which requires more robust, predictable and high throughput methods. In this mini-review we highlight recent progress in the areas of improving transgene expression, genome editing, identification and design of standard genetic elements (parts), and the use of microfluidics to increase throughput. We suggest that combining these approaches will provide the means to establish algal synthetic biology, and that application of standard parts and workflows will avoid parallel development and capitalize on lessons learned from other systems.
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June 2016
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Cover Image
Shining a spotlight on outer membrane protein folding. Outer membrane proteins (OMPs) [such as OmpA (green, top left)] have to navigate their way from the ribosome (bottom of image) via trigger factor (red) and SecB (turquoise), through the SecYEG translocon (red/yellow) in the inner membrane (IM). They are then chaperoned across the periplasm until they can insert and fold into their ultimate destination, the outer membrane. For further details see pp. 802–809. The figure was produced by Jim Horne. - PDF Icon PDF LinkTable of Contents
Review Article|
June 09 2016
Towards developing algal synthetic biology
Mark Aden Scaife;
Mark Aden Scaife
1
*Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge, CB2 3EA U.K.
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Alison Gail Smith
Alison Gail Smith
1
*Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge, CB2 3EA U.K.
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Publisher: Portland Press Ltd
Received:
February 12 2016
Online ISSN: 1470-8752
Print ISSN: 0300-5127
© 2016 The Author(s). published by Portland Press Limited on behalf of the Biochemical Society
2016
Biochem Soc Trans (2016) 44 (3): 716–722.
Article history
Received:
February 12 2016
Citation
Mark Aden Scaife, Alison Gail Smith; Towards developing algal synthetic biology. Biochem Soc Trans 15 June 2016; 44 (3): 716–722. doi: https://doi.org/10.1042/BST20160061
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