GROWTH-PROCESSES IN BIOREACTORS WITH EXTERNAL SOURCES OF BIOMASS - APPLICATION OF STRUCTURED, CONTINUUM MODELS

被引:5
作者
FREDRICKSON, AG [1 ]
机构
[1] UNIV MINNESOTA,INST ADV STUDIES BIOL PROC TECHNOL,DEPT CHEM ENGN & MAT SCI,ST PAUL,MN 55108
关键词
D O I
10.1002/aic.690380605
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Batch, fed-batch, and single-stage CSTR bioreactors operate without external sources of biomass after they have been inoculated. However, other kinds of bioreators, such as the second and subsequent reactors in a cascade of CSTRs, operate with continuous introduction of biomass from one or more external sources. The biomass in a bioreactor with an external source is not homogeneous with respect to past history of environmental conditions, and growth of this biomass is not balanced (steady-state) growth even when the bioreactor operates in steady state. So-called unstructured models of growth, which assume biomass to lack any internal structure or to have an invariant internal state, can give only a first approximation to the growth rate behavior of the biomass in a bioreactor with an external source of biomass. Structured models, which endow biomass with a changeable internal structure, are required to obtain more accurate predictions of growth rate behavior in such reactors. Introduction of structure is not sufficient for improved accuracy, however, and the fact that biomasses from different sources are and remain segregated from one another must also be accounted for by any structured growth model used. This article presents, among others, the systems of different equations that result from application of the notions to the reactors of a cascade of CSTRs.
引用
收藏
页码:835 / 846
页数:12
相关论文
共 21 条
[1]  
Bailey J., 1986, BIOCH ENG FUNDAMENTA, DOI 10.1016/0168-3659(86)90022-2
[2]  
BALOO S, 1992, BIOTECHNOL BIOENG, V38, P1337
[3]  
BALOO S, 1992, BIOTECHNOL BIOENG, V38, P1353
[4]   A STRUCTURED MODEL FOR MONOCLONAL-ANTIBODY SYNTHESIS IN EXPONENTIALLY GROWING AND STATIONARY PHASE HYBRIDOMA CELLS [J].
BIBILA, T ;
FLICKINGER, MC .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 37 (03) :210-226
[5]   A MODEL OF INTERORGANELLE MONOCLONAL-ANTIBODY TRANSPORT AND SECRETION IN MOUSE HYBRIDOMA CELLS [J].
BIBILA, TA ;
FLICKINGER, MC .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 38 (07) :767-780
[6]  
BONOMI A, 1979, REVIS BRAS TEC, V10, P217
[7]   OPTIMAL CHEMOSTAT CASCADES FOR PERIPLASMIC PROTEIN-PRODUCTION [J].
DAVIS, RH ;
RAMIREZ, WF ;
CHATTERJEE, A .
BIOTECHNOLOGY PROGRESS, 1990, 6 (06) :430-436
[8]  
FREDERICKSON A. G., 1967, MATH BIO SCL, V1, P327, DOI 10.1016/0025-5564(67)90008-9
[9]  
FREDRICKSON A G, 1971, Chemical Engineering Progress Symposium Series, V67, P53
[10]  
Fredrickson A.G., 1970, ADV APPL MICROBIO, V13, P419, DOI [10.1016/S0065-2164(08)70413-1, DOI 10.1016/S0065-2164(08)70413-1]