Bioprocess intensification for production of novel marine bacterial antibiotics through bioreactor operation and design

被引:40
作者
Marwick, JD
Wright, PC [1 ]
Burgess, JG
机构
[1] Heriot Watt Univ, Dept Mech & Chem Engn, Edinburgh EH14 4AS, Midlothian, Scotland
[2] Heriot Watt Univ, Dept Biol Sci, Edinburgh EH14 4AS, Midlothian, Scotland
关键词
natural products; antibiotics; marine bacteria; bioreactor; bioprocess intensification;
D O I
10.1007/PL00011806
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
There is a lack of research into bioreactor engineering and fermentation protocol design in the field of marine bacterial antibiotic production. Most production strategies are carried out at the shake-flask level and lack a mechanistic understanding of the antibiotic production process, offering poor prospects for successful scale-up. This review shows that data need to be collated on media and physical optima differences between the trophophase and idiophase, along with investigations into the control mechanisms for biosynthesis, to anew implementation of novel fermentation protocols. Immobilization may play a part in bioprocess intensification of marine bacterial antibiotic production, through again this area is understudied. Similarly, mass transfer and shear stress data of fermentations are needed to provide the bioreactor design requirements to intensify antibiotic biosynthesis, with process scale-up in mind. The application of bioprocess intensification methods to the production of antibiotics (and other metabolites) from marine microbes will become an important strategy for improving supply of natural products, in order to assess their suitability as chemotherapeutic drugs.
引用
收藏
页码:495 / 507
页数:13
相关论文
共 134 条
[1]   NITROGEN METABOLITE REGULATION OF ANTIBIOTIC BIOSYNTHESIS [J].
AHARONOWITZ, Y .
ANNUAL REVIEW OF MICROBIOLOGY, 1980, 34 :209-233
[2]   AUTOTOXIC ANTIBIOTIC PRODUCTION BY A MARINE CHROMOBACTERIUM [J].
ANDERSEN, RJ ;
WOLFE, MS ;
FAULKNER, DJ .
MARINE BIOLOGY, 1974, 27 (04) :281-285
[3]   PLASMID TRANSFER BETWEEN MARINE-BACTERIA IN THE AQUEOUS PHASE AND BIOFILMS IN REACTOR MICROCOSMS [J].
ANGLES, ML ;
MARSHALL, KC ;
GOODMAN, AE .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (03) :843-850
[4]   MICROBIAL ATTACHMENT AND GROWTH IN FIXED-FILM REACTORS - PROCESS STARTUP CONSIDERATIONS [J].
ANNACHHATRE, AP ;
BHAMIDIMARRI, SMR .
BIOTECHNOLOGY ADVANCES, 1992, 10 (01) :69-91
[5]  
Bailey JE., 1986, BIOCH ENG FUNDAMENTA, P421
[6]   UTILIZATION OF CARBON AND NITROGEN SOURCES BY STREPTOMYCES-KANAMYCETICUS FOR KANAMYCIN PRODUCTION [J].
BASAK, K ;
MAJUMDAR, SK .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1973, 4 (01) :6-10
[7]   Cross-species induction of luminescence in the quorum-sensing bacterium Vibrio harveyi [J].
Bassler, BL ;
Greenberg, EP ;
Stevens, AM .
JOURNAL OF BACTERIOLOGY, 1997, 179 (12) :4043-4045
[8]  
BEETON S, 1994, APPL MICROBIOL BIOT, V40, P812
[9]   GAS TRANSFER CHARACTERISTICS OF A NOVEL MEMBRANE BIOREACTOR [J].
BEETON, S ;
MILLWARD, HR ;
BELLHOUSE, BJ ;
NICHOLSON, AM ;
JENKINS, N ;
KNOWLES, CJ .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 38 (10) :1233-1238
[10]   ANHYDROTETRACYCLINE OXYGENASE ACTIVITY AND BIOSYNTHESIS OF TETRACYCLINES IN STREPTOMYCES AUREOFACIENS [J].
BEHAL, V ;
HOSTALEK, Z ;
VANEK, Z .
BIOTECHNOLOGY LETTERS, 1979, 1 (04) :177-182