The Role of Cell Wall Revealed by the Visualization of Saccharomyces cerevisiae Transformation

被引:11
作者
Pham, Tuan Anh [1 ]
Kawai, Shigeyuki [1 ]
Kono, Emi [1 ]
Murata, Kousaku [1 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Lab Basic & Appl Mol Biotechnol, Kyoto 6110011, Japan
关键词
INTACT YEAST-CELLS; POLYETHYLENE-GLYCOL; PATHWAY; DNA; COMPARTMENTS; MICROSCOPY; FUSION; GENE; CA2+;
D O I
10.1007/s00284-010-9807-y
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Transformation is an indispensable method for the manipulation of Saccharomyces cerevisiae cell. The spf1 cell, in which the gene encoding an endoplasmic reticulum-located P-type ATPase is deleted, has been known to show the high-transformation phenotype. In this study, fluorescent microscopic observation of transformation process of S. cerevisiae using plasmid DNA labelled with fluorescent DNA probe, YOYO-1, suggested that the spf1 cell absorbed more plasmid DNA on cellular surface than did the wild-type cell and the unwashed cell did more plasmid DNA than the washed cell. The amounts of the absorbed DNA correlated with the transformation efficiency (number of transformants per mu g plasmid DNA) and frequency (transformation efficiency per viable cell number). The high-transformation phenotype of spf1 cell and the effect of heat shock, which effectively induces the transformation of intact cell, disappeared upon cell wall digestion. Electron microscopic observation of the transformation process using negatively charged Nanogold as a mimic of plasmid DNA supported the result obtained using YOYO-1 and implied that plasmid DNA enters into cell together with membrane structure. These data strongly suggest that during the transformation of intact cell, plasmid DNA is initially absorbed on the cell wall, passes through the cell wall with the aid of heat shock, reaches to the membrane, and enters into the cell together with the membrane structure and that the capacity of the cell wall to absorb DNA is at least one of the determinants of transformation efficiency and frequency.
引用
收藏
页码:956 / 961
页数:6
相关论文
共 25 条
[1]  
[Anonymous], METHOD ENZYMOL
[2]   ELECTRON MICROSCOPY IN YEAST [J].
Baba, Misuzu .
AUTOPHAGY: LOWER EUKARYOTES AND NON-MAMMALIAN SYSTEMS, PT A, 2008, 451 :133-149
[3]   TRANSFORMATION OF YEAST SPHEROPLASTS WITHOUT CELL-FUSION [J].
BURGERS, PMJ ;
PERCIVAL, KJ .
ANALYTICAL BIOCHEMISTRY, 1987, 163 (02) :391-397
[4]   Visualized investigation of yeast transformation induced with Li+ and polyethylene glycol [J].
Chen, Ping ;
Liu, Hui-Hui ;
Cui, Ran ;
Zhang, Zhi-Ling ;
Pang, Dai-Wen ;
Xie, Zhi-Xiong ;
Zheng, Hu-Zhi ;
Lu, Zhe-Xue ;
Tong, Hua .
TALANTA, 2008, 77 (01) :262-268
[5]   Cod1p/Spf1p is a P-type ATPase involved in ER function and Ca2+ homeostasis [J].
Cronin, SR ;
Rao, RJ ;
Hampton, RY .
JOURNAL OF CELL BIOLOGY, 2002, 157 (06) :1017-1028
[6]   The medial-Golgi ion pump Pmr1 supplies the yeast secretory pathway with Ca2+ and Mn2+ required for glycosylation, sorting, and endoplasmic reticulum associated protein degradation [J].
Dürr, G ;
Strayle, J ;
Plemper, R ;
Elbs, S ;
Klee, SK ;
Catty, P ;
Wolf, DH ;
Rudolph, HK .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (05) :1149-1162
[7]   Genetic transformation of yeast [J].
Gietz, RD ;
Woods, RA .
BIOTECHNIQUES, 2001, 30 (04) :816-+
[8]   STUDIES ON THE TRANSFORMATION OF INTACT YEAST-CELLS BY THE LIAC/S-DNA/PEG PROCEDURE [J].
GIETZ, RD ;
SCHIESTL, RH ;
WILLEMS, AR ;
WOODS, RA .
YEAST, 1995, 11 (04) :355-360
[9]  
Gietz RD, 2002, METHOD ENZYMOL, V350, P87
[10]   Ultrastructural Analysis of Nanogold-labeled Endocytic Compartments of Yeast Saccharomyces cerevisiae Using a Cryosectioning Procedure [J].
Griffith, Janice ;
Reggiori, Fulvio .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2009, 57 (08) :801-809