INDUSTRIAL-PRODUCTION OF HETEROLOGOUS PROTEINS BY FED-BATCH CULTURES OF THE YEAST SACCHAROMYCES-CEREVISIAE

被引:53
作者
MENDOZAVEGA, O
SABATIE, J
BROWN, SW
机构
关键词
SACCHAROMYCES CEREVISIAE; FED BATCH; MICROBIAL PHYSIOLOGY; GENETICS; BIOPROCESS DESIGN;
D O I
10.1111/j.1574-6976.1994.tb00146.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This review concerns the issues involved in the industrial development of fed-batch culture processes with Saccharomyces cerevisiae strains producing heterologous proteins. Most of process development considerations with fed-batch recombinant cultures:are linked to the reliability and reproducibility of the process for manufacturing environments where quality assurance and quality control aspects are paramount. In this respect, the quality, safety and efficacy of complex biologically active molecules produced by recombinant techniques are strongly influenced by the genetic background of the host strain, genetic stability of the transformed strain and production process factors. An overview of the recent literature of these culture-related factors is coupled with our experience in yeast fed-batch process development for producing various therapeutic grade proteins. The discussion is based around three principal topics: genetics, microbial physiology and fed-batch process design. It includes the fundamental aspects of yeast strain physiology, the nature of the recombinant product, quality control aspects of the biological product, features of yeast expression vectors, expression and localization of recombinant products in transformed cells and fed-batch process considerations for the industrial production of Saccharomyces cerevisiae recombinant proteins. It is our purpose that this review will provide a comprehensive understanding of the fed-batch recombinant production processes and challenges commonly encountered during process development.
引用
收藏
页码:369 / 410
页数:42
相关论文
共 194 条
[61]  
Fleer Reinhard, 1992, Current Opinion in Biotechnology, V3, P486, DOI 10.1016/0958-1669(92)90076-U
[62]   TANDEM GENE AMPLIFICATION MEDIATES COPPER RESISTANCE IN YEAST [J].
FOGEL, S ;
WELCH, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (17) :5342-5346
[63]   INACTIVATION OF FRUCTOSE-1,6-DIPHOSPHATASE BY GLUCOSE IN YEAST [J].
GANCEDO, C .
JOURNAL OF BACTERIOLOGY, 1971, 107 (02) :401-&
[64]   INACTIVATION BY GLUCOSE OF PHOSPHOENOLPYRUVATE CARBOXYKINASE FROM SACCHAROMYCES-CEREVISIAE [J].
GANCEDO, C ;
SCHWERZMANN, K .
ARCHIVES OF MICROBIOLOGY, 1976, 109 (03) :221-225
[65]  
GANCEDO JM, 1986, FEMS MICROBIOL LETT, V32, P179
[66]   CARBON CATABOLITE REPRESSION IN YEAST [J].
GANCEDO, JM .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 206 (02) :297-313
[67]  
GARRIDO-SANCHEZ L E, 1988, Biotechnology Techniques, V2, P17, DOI 10.1007/BF01874202
[68]   HIGH-LEVEL EXPRESSION OF FOREIGN GENES IN HANSENULA-POLYMORPHA [J].
GELLISSEN, G ;
JANOWICZ, ZA ;
WEYDEMANN, U ;
MELBER, K ;
STRASSER, AWM ;
HOLLENBERG, CP .
BIOTECHNOLOGY ADVANCES, 1992, 10 (02) :179-189
[69]   A COMPARISON OF DIFFERENT TECHNIQUES FOR THE CONTROL OF THE GROWTH OF CANDIDA-UTILIS CBS-621 [J].
GHOUL, M ;
BOUDRANT, J ;
ENGASSER, JM .
PROCESS BIOCHEMISTRY, 1991, 26 (03) :135-142
[70]  
GHOUL M, 1985, THESIS I NATIONAL PO