Using inactivated microbial biomass as fertilizer:: the fate of antibiotic resistance genes in the environment

被引:18
作者
Andersen, JT [1 ]
Schäfer, T [1 ]
Jorgensen, PL [1 ]
Moller, S [1 ]
机构
[1] Novozymes AS, DK-2880 Bagsvaerd, Denmark
关键词
biomass; fertilizer; bacteria; DNA determination; soil; gene transfer;
D O I
10.1016/S0923-2508(01)01266-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The waste product produced by Novo Nordisk A/S from microbial fermentations is used as agricultural fertilizer in Denmark (NovoGro (TM)) after being treated by heat and chemicals to destroy the microorganisms. The fertilizer contains DNA fragments from the genetically modified microorganisms used in industrial production. This DNA contains genes coding for the desired industrial products as well as genes used as genetic selection markers during production strain development. The antibiotic resistance markers used as genetic selection markers are chloramphenicol (Cm), kanamycin (Km) and ampicillin (Ap). The aim of the present study Was to examine whether DNA and intact genes were present in NovoGro and whether horizontal transfer of DNA isolated from inactivated production strains occurred either in the laboratory or in the fields treated with NovoGro. DNA isolated from NovoGro was analysed by PCR and intact genes coding for a protease and chloramphenicol resistance were amplified. This isolated DNA was used for in vitro experiments including electroporation and transformation but no transfer of DNA to Escherichia coli or Bacillus subtilis was observed. The antibiotic resistance profile of the indigenous bacterial population in the fields treated with NovoGro compared with fields treated with inorganic fertilizers showed no differences. In addition, DNA isolated directly from the fields treated with NovoGro for up to 7 years was analysed by PCR and no specific production gene constructs could be detected. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:823 / 833
页数:11
相关论文
共 36 条
[1]   PHYLOGENETIC IDENTIFICATION AND IN-SITU DETECTION OF INDIVIDUAL MICROBIAL-CELLS WITHOUT CULTIVATION [J].
AMANN, RI ;
LUDWIG, W ;
SCHLEIFER, KH .
MICROBIOLOGICAL REVIEWS, 1995, 59 (01) :143-169
[2]   Horizontal gene transfers in the environment: natural transformation as a putative process for gene transfers between transgenic plants and microorganisms [J].
Bertolla, F ;
Simonet, P .
RESEARCH IN MICROBIOLOGY, 1999, 150 (06) :375-384
[3]   HIGH-FREQUENCY OF CONJUGATION VERSUS PLASMID SEGREGATION OF RP1 IN EPIPHYTIC PSEUDOMONAS-SYRINGAE POPULATIONS [J].
BJORKLOF, K ;
SUONIEMI, A ;
HAAHTELA, K ;
ROMANTSCHUK, M .
MICROBIOLOGY-UK, 1995, 141 :2719-2727
[4]   Construction and use of a versatile set of broad-host-range cloning and expression vectors based on the RK2 replicon [J].
Blatny, JM ;
Brautaset, T ;
WintherLarsen, HC ;
Haugan, K ;
Valla, S .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (02) :370-379
[5]   A review of available systems to investigate transfer of DNA to indigenous soil bacteria [J].
Clerc, S ;
Simonet, P .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 1998, 73 (01) :15-23
[6]   MULTIPLE ANTIBIOTIC-RESISTANCE IN RHIZOBIUM-JAPONICUM [J].
COLE, MA ;
ELKAN, GH .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1979, 37 (05) :867-870
[7]   Genetic exchange between bacteria in the environment [J].
Davison, J .
PLASMID, 1999, 42 (02) :73-91
[8]   CLONING OF ALDB, WHICH ENCODES ALPHA-ACETOLACTATE DECARBOXYLASE, AN EXOENZYME FROM BACILLUS-BREVIS [J].
DIDERICHSEN, B ;
WEDSTED, U ;
HEDEGAARD, L ;
JENSEN, BR ;
SJOHOLM, C .
JOURNAL OF BACTERIOLOGY, 1990, 172 (08) :4315-4321
[9]  
Doblhoff-Dier O, 2000, TRENDS BIOTECHNOL, V18, P141
[10]   Tansley Review No. 99 - The release of genetically engineered micro-organisms and viruses into the environment [J].
Giddings, G .
NEW PHYTOLOGIST, 1998, 140 (02) :173-184