Synthetic Biology 2013
DOI: 10.1016/b978-0-12-394430-6.00001-7
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New Tools for Cost-Effective DNA Synthesis

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Cited by 15 publications
(8 citation statements)
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“…Analysis of cells produced by SCRaMbLE can reveal how changes in genome structure influence particular phenotypes or can be used to screen for Box 1 | Methods for building and activating chromosomes Assembly of large DNA molecules: Chromosomes are synthesized through the hierarchical assembly of smaller DNA molecules into progressively larger ones. This process begins with molecules that are hundreds of base pairs in length ("fragments"), which can be readily ordered from commercial vendors and are reviewed elsewhere 134,135 . Fragments are typically combined together and cloned into bacterial plasmids by Gibson 113,136,137 or Golden Gate 138,139 assembly.…”
Section: Genetic Manipulations Enabled By Synthetic Genomicsmentioning
confidence: 99%
“…Analysis of cells produced by SCRaMbLE can reveal how changes in genome structure influence particular phenotypes or can be used to screen for Box 1 | Methods for building and activating chromosomes Assembly of large DNA molecules: Chromosomes are synthesized through the hierarchical assembly of smaller DNA molecules into progressively larger ones. This process begins with molecules that are hundreds of base pairs in length ("fragments"), which can be readily ordered from commercial vendors and are reviewed elsewhere 134,135 . Fragments are typically combined together and cloned into bacterial plasmids by Gibson 113,136,137 or Golden Gate 138,139 assembly.…”
Section: Genetic Manipulations Enabled By Synthetic Genomicsmentioning
confidence: 99%
“…Once the digital file is encoded, the next step is to synthesize arbitrary single-strand DNA sequences chemically, nucleotide by nucleotide. There are several methods for de novo DNA sequence synthesis chemical oligonucleotide synthesis (phosphoramidite oligonucleotide synthesis) and oligo synthesis platforms using ink-jet printing (Agilent, Protogene), photosensitive 5' deprotection (Nimblegen, Affymetrix), photolithography (Invitrogen) and electrochemical arrays (Oxamer) with 20 to 90 oligomers synthesizing capacity at least error rate (Tang et al, 2013). Once we generate DNA oligomers or sequence that coded for digital information, DNA can be deep freeze at -20° to -80°C temperatures for a long time or till needed to decode through sequencing to recovered digital information.…”
Section: How D I G I Ta L I N F O R M At I O N C a N B E S To R E D Imentioning
confidence: 99%
“…While further reduction of the synthesis cost using the traditional column-based methods is unlikely, microarray-based technologies provide great potential for high-throughput and cost-effective DNA synthesis, as discussed in details elsewhere (Mueller, Coleman, 2009, Tang et al, 2013). Here we will focus on two recent advances in microarray-based DNA synthesis, highlighting the importance of technology integration.…”
Section: Genome Synthesismentioning
confidence: 99%