A Simple and Immediate Method for Simultaneously Evaluating Expression Level and Plasmid Maintenance in Yeast

被引:88
作者
Ishii, Jun [2 ]
Izawa, Keiko [1 ]
Matsumura, Shizuka [1 ]
Wakamura, Kanako [1 ]
Tanino, Takanori [1 ]
Tanaka, Tsutomu [2 ]
Ogino, Chiaki [1 ]
Fukuda, Hideki [2 ]
Kondo, Akihiko [1 ]
机构
[1] Kobe Univ, Dept Chem Sci & Engn, Grad Sch Engn, Kobe, Hyogo, Japan
[2] Kobe Univ, Org Adv Sci & Technol, Kobe, Hyogo, Japan
关键词
yeast; expression system; plasmid maintenance; green fluorescent protein; flow cytometry; SACCHAROMYCES-CEREVISIAE; HETEROLOGOUS PROTEINS; SHUTTLE VECTORS; SYSTEM; DNA; RECOVERY; STRAINS; CELLS;
D O I
10.1093/jb/mvp028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To allow the comprehensive assessments of yeast expression systems, a simple and immediate method for simultaneously evaluating the expression level and plasmid maintenance in yeast was demonstrated. This method uses green fluorescent protein (GFP) and flow cytometry (FCM) and is characterized by a dual analysis of the average intensity of GFP fluorescence and the population of GFP-expressing cells. The FCM analysis of GFP fluorescence intensity rapidly quantifies the expression level without complex manipulations, such as the enzymatic reaction of a lacZ reporter assay. Moreover, the single-cell analysis revealed that the proportion of cells expressing GFP in the cell cluster reflects the plasmid retention rate; therefore, the FCM analysis of the GFP-expressing population allows the immediate estimation of the plasmid retention rate without the 2- or 3-day incubation required for colony counting. We show that the FCM analysis with GFP reporter is a suitable method to explore the hopeful expression vector and host strain or establish the several expression systems exhibiting the characteristic properties in yeast.
引用
收藏
页码:701 / 708
页数:8
相关论文
共 14 条
[1]   STERILE HOST YEASTS (SHY) - EUKARYOTIC SYSTEM OF BIOLOGICAL CONTAINMENT FOR RECOMBINANT DNA EXPERIMENTS [J].
BOTSTEIN, D ;
FALCO, SC ;
STEWART, SE ;
BRENNAN, M ;
SCHERER, S ;
STINCHCOMB, DT ;
STRUHL, K ;
DAVIS, RW .
GENE, 1979, 8 (01) :17-24
[2]  
Brachmann CB, 1998, YEAST, V14, P115
[3]   YEAST SYSTEMS FOR THE COMMERCIAL PRODUCTION OF HETEROLOGOUS PROTEINS [J].
BUCKHOLZ, RG ;
GLEESON, MAG .
BIO-TECHNOLOGY, 1991, 9 (11) :1067-1072
[4]   MULTIFUNCTIONAL YEAST HIGH-COPY-NUMBER SHUTTLE VECTORS [J].
CHRISTIANSON, TW ;
SIKORSKI, RS ;
DANTE, M ;
SHERO, JH ;
HIETER, P .
GENE, 1992, 110 (01) :119-122
[5]   High-efficiency recovery of target cells using improved yeast display system for detection of protein-protein interactions [J].
Fukuda, Nobuo ;
Ishii, Jun ;
Shibasaki, Seiji ;
Ueda, Mitsuyoshi ;
Fukuda, Hideki ;
Kondo, Akihiko .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2007, 76 (01) :151-158
[6]   IMPROVED METHOD FOR HIGH-EFFICIENCY TRANSFORMATION OF INTACT YEAST-CELLS [J].
GIETZ, D ;
STJEAN, A ;
WOODS, RA ;
SCHIESTL, RH .
NUCLEIC ACIDS RESEARCH, 1992, 20 (06) :1425-1425
[7]   NUCLEOTIDE-SEQUENCE OF THE YEAST PLASMID [J].
HARTLEY, JL ;
DONELSON, JE .
NATURE, 1980, 286 (5776) :860-865
[8]   Yeast-based fluorescence reporter assay of G protein-coupled receptor signalling for flow cytometric screening:: FAR1-disruption recovers loss of episomal plasmid caused by signalling in yeast [J].
Ishii, Jun ;
Tanaka, Tsutomu ;
Matsumura, Shizuka ;
Tatematsu, Kenji ;
Kuroda, Shun'ichi ;
Ogino, Chiaki ;
Fukuda, Hideki ;
Kondo, Akihiko .
JOURNAL OF BIOCHEMISTRY, 2008, 143 (05) :667-674
[9]  
Kanai T, 1996, APPL MICROBIOL BIOT, V44, P759, DOI 10.1007/s002530050629
[10]   YEAST VECTORS FOR THE CONTROLLED EXPRESSION OF HETEROLOGOUS PROTEINS IN DIFFERENT GENETIC BACKGROUNDS [J].
MUMBERG, D ;
MULLER, R ;
FUNK, M .
GENE, 1995, 156 (01) :119-122