STATE-OF-THE-ART AND FUTURE-DEVELOPMENTS IN FERMENTATION

被引:0
|
作者
MASSCHELEIN, CA [1 ]
机构
[1] VRIJE UNIV BRUSSELS,INST BIOTECHNOL,B-1070 BRUSSELS,BELGIUM
关键词
ALCOHOL-FREE BEER; CONTINUOUS PROCESS; CYLINDROCONICAL TANK; FERMENTATION CONDITIONS; FLAVOR FORMATION; IMMOBILIZED CELL; MATURATION; YEAST TECHNOLOGY;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The objective of process optimization in brewery fermentations is to build up yeast concentrations sufficient to gain an optimal rate and extent of attenuation and desired flavor development, while balancing, but not overexpending, wort nutrients for growth and maintenance. In terms of process economics, two alternatives exist-moving to greater volume accelerated-batch processing and applying small-scale, high-rate fermentation systems that are capable of being stepped up to meet peak output when necessary. In the standard batch process, volumetric productivities are controlled mainly by cyclic variations in growth and fermentation rates and by the amount of yeast in suspension as a result of the gas-lift action taking place in the fermentor. Thus, fermentor design must be optimized with respect to agitation and yeast concentration. Reduced process times may be achieved in cylindroconical vessels because of increased movement within the fermentor. Unfortunately, high degrees of agitation have been shown to give flavor problems. The adverse effects of agitation on beer quality may be prevented by operating under fed-batch conditions. Another approach to improve volumetric productivity is cell immobilization. With the successful application of immobilized yeast reactors for continuous beer maturation, as well as for the production of low-alcohol and nonalcoholic beers, one can expect an increasing contribution of immobilized yeast systems to the development of a new process area in the brewing industry.
引用
下载
收藏
页码:28 / 35
页数:8
相关论文
共 50 条
  • [21] TRANSDERMAL THERAPEUTIC SYSTEMS - ACTUAL STATE AND FUTURE-DEVELOPMENTS
    ASMUSSEN, B
    METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, 1991, 13 (05): : 343 - 351
  • [22] FUTURE-DEVELOPMENTS IN IMAGING
    ROBB, WL
    INVESTIGATIVE RADIOLOGY, 1993, 28 : S119 - S120
  • [23] FUTURE-DEVELOPMENTS IN PHENYLKETONURIA
    DANKS, DM
    COTTON, RGH
    ENZYME, 1987, 38 (1-4) : 296 - 301
  • [24] STRUCTURAL EQUATION MODELLING IN THE GENOMICS ERA: STATE-OF-THE-ART AND FUTURE DEVELOPMENTS
    Barendse, Mariska
    Klassmann, Alexander
    de Hoyos, Lucia
    Rai, Dheeraj
    Fisher, Simon
    St Pourcain, Beate
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2021, 51 : E80 - E81
  • [25] POSSIBLE FUTURE-DEVELOPMENTS
    不详
    MENTAL HOSPITALS, 1960, 11 (02): : 43 - &
  • [26] FUTURE-DEVELOPMENTS OF GALVANOTECHNIQUE
    RAUB, CJ
    METALL, 1987, 41 (03): : 283 - 286
  • [27] DEFICIENCIES AND FUTURE-DEVELOPMENTS
    OLLENSCHLAGER, G
    MEDIZINISCHE KLINIK, 1995, 90 (08) : 486 - 489
  • [28] FUTURE-DEVELOPMENTS IN LAMPS
    CAYLESS, MA
    IEE PROCEEDINGS-A-SCIENCE MEASUREMENT AND TECHNOLOGY, 1980, 127 (03): : 211 - 218
  • [29] Using reference models for business engineering state-of-the-art and future developments
    Fettke, Peter
    Loos, Peter
    2006 INNOVATIONS IN INFORMATION TECHNOLOGY, 2006, : 427 - +
  • [30] Nanomedicine for treatment of diabetes in an aging population: State-of-the-art and future developments
    Krol, Silke
    Ellis-Behnke, Rutledge
    Marchetti, Piero
    MATURITAS, 2012, 73 (01) : 61 - 67