Yeast

From 2012.igem.org

(Difference between revisions)
Line 15: Line 15:
<h3>Shuttle vectors</h3>   
<h3>Shuttle vectors</h3>   
<p> Today, most commonly encountered S. cerevisiae shuttle vectors belong to one of three classes:
<p> Today, most commonly encountered S. cerevisiae shuttle vectors belong to one of three classes:
-
-Integrating plasmids YIp
+
-Integrating plasmids YIp<br/>
-
-Centromere plasmids YCp
+
-Centromere plasmids YCp<br/>
-
-Yeast episomal plasmids  YEp
+
-Yeast episomal plasmids  YEp<br/>
The name pRS415 Gives an indication on the presence of a CEN/ARS replication origin. 0 means yeast
The name pRS415 Gives an indication on the presence of a CEN/ARS replication origin. 0 means yeast
integrative plasmid, 1 means that it also can be used to maintain the plasmid in circular
integrative plasmid, 1 means that it also can be used to maintain the plasmid in circular

Revision as of 22:13, 25 September 2012

Menu

Receptor

Yeast for dummies

Since this is the first time that TU Delfts iGEM team is working with yeast, we faced a lot of small yeast-related 'challenges'. With this page we want to inform you about the basics and the pitfalls of working with yeast.

Auxotrophy

Shuttle vectors

Today, most commonly encountered S. cerevisiae shuttle vectors belong to one of three classes: -Integrating plasmids YIp
-Centromere plasmids YCp
-Yeast episomal plasmids YEp
The name pRS415 Gives an indication on the presence of a CEN/ARS replication origin. 0 means yeast integrative plasmid, 1 means that it also can be used to maintain the plasmid in circular form. pRS415 Gives an indication of the auxotrophic marker used. pRS415 Version number… not really different.

Chromosomal integration

We encountered a lot of problems with plasmids. Because we wanted our constructs to be universal (with the idea to make it suitable for ‘fast checking’) we tried maintaining a plasmid. As it turned out, yeast cells are not eager to maintain a plasmid and with our construct we suspect homologous recombination occurred. After transformation, a PCR on the transformed plasmid, obtained by isolation, showed two bands instead of the suspected single band, one being ! Integration of the plasmid is therefore advised! Checking of this can be quite gruesome optimizing the necessary PCR reactions on your transformed yeast colonies. Chromosomal isolation can therefore improve the steps.


Knock-out strains

Nomenclature