Rapid Golden Gate assembly of exons from genomic DNA for protein expression in Escherichia coli and Pichia pastoris

The development of a quick, single-step cloning system for generation of multiexon gene expression constructs is presented. The system allows efficient and cost-effective assembly of multiple exons of interest genes into different expression plasmids in both Escherichia coli and Pichia pastoris. The...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:BioTechniques. - 1993. - 71(2021), 2 vom: 01. Aug., Seite 445-450
1. Verfasser: Cheng, Junhao (VerfasserIn)
Weitere Verfasser: Wu, Mingkun, Zhong, Ren, Si, Dayong, Meng, Geng, Zhang, Rijun, Zhang, Yueping
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2021
Zugriff auf das übergeordnete Werk:BioTechniques
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Escherichia coli Golden Gate Pichia pastoris heterologous expression quick exon assembly Recombinant Proteins DNA 9007-49-2
LEADER 01000caa a22002652c 4500
001 NLM329184059
003 DE-627
005 20250302083242.0
007 cr uuu---uuuuu
008 231225s2021 xx |||||o 00| ||eng c
024 7 |a 10.2144/btn-2021-0039  |2 doi 
028 5 2 |a pubmed25n1097.xml 
035 |a (DE-627)NLM329184059 
035 |a (NLM)34374327 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Cheng, Junhao  |e verfasserin  |4 aut 
245 1 0 |a Rapid Golden Gate assembly of exons from genomic DNA for protein expression in Escherichia coli and Pichia pastoris 
264 1 |c 2021 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 20.12.2021 
500 |a Date Revised 20.12.2021 
500 |a published: Print-Electronic 
500 |a Citation Status MEDLINE 
520 |a The development of a quick, single-step cloning system for generation of multiexon gene expression constructs is presented. The system allows efficient and cost-effective assembly of multiple exons of interest genes into different expression plasmids in both Escherichia coli and Pichia pastoris. The high cloning efficiency and low cost of the system make it ideal for a novel workflow for the assembly of intron-bearing genes for expression in two different expression hosts 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Escherichia coli 
650 4 |a Golden Gate 
650 4 |a Pichia pastoris 
650 4 |a heterologous expression 
650 4 |a quick exon assembly 
650 7 |a Recombinant Proteins  |2 NLM 
650 7 |a DNA  |2 NLM 
650 7 |a 9007-49-2  |2 NLM 
700 1 |a Wu, Mingkun  |e verfasserin  |4 aut 
700 1 |a Zhong, Ren  |e verfasserin  |4 aut 
700 1 |a Si, Dayong  |e verfasserin  |4 aut 
700 1 |a Meng, Geng  |e verfasserin  |4 aut 
700 1 |a Zhang, Rijun  |e verfasserin  |4 aut 
700 1 |a Zhang, Yueping  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t BioTechniques  |d 1993  |g 71(2021), 2 vom: 01. Aug., Seite 445-450  |w (DE-627)NLM012627046  |x 1940-9818  |7 nnas 
773 1 8 |g volume:71  |g year:2021  |g number:2  |g day:01  |g month:08  |g pages:445-450 
856 4 0 |u http://dx.doi.org/10.2144/btn-2021-0039  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_21 
912 |a GBV_ILN_22 
912 |a GBV_ILN_39 
912 |a GBV_ILN_40 
912 |a GBV_ILN_50 
912 |a GBV_ILN_60 
912 |a GBV_ILN_62 
912 |a GBV_ILN_65 
912 |a GBV_ILN_70 
912 |a GBV_ILN_99 
912 |a GBV_ILN_121 
912 |a GBV_ILN_130 
912 |a GBV_ILN_227 
912 |a GBV_ILN_350 
912 |a GBV_ILN_618 
912 |a GBV_ILN_640 
912 |a GBV_ILN_754 
912 |a GBV_ILN_2001 
912 |a GBV_ILN_2002 
912 |a GBV_ILN_2003 
912 |a GBV_ILN_2005 
912 |a GBV_ILN_2006 
912 |a GBV_ILN_2007 
912 |a GBV_ILN_2008 
912 |a GBV_ILN_2009 
912 |a GBV_ILN_2010 
912 |a GBV_ILN_2012 
912 |a GBV_ILN_2015 
912 |a GBV_ILN_2018 
912 |a GBV_ILN_2023 
912 |a GBV_ILN_2035 
912 |a GBV_ILN_2040 
912 |a GBV_ILN_2060 
912 |a GBV_ILN_2099 
912 |a GBV_ILN_2105 
912 |a GBV_ILN_2121 
912 |a GBV_ILN_2470 
951 |a AR 
952 |d 71  |j 2021  |e 2  |b 01  |c 08  |h 445-450