The Center for Biochemical Engineering, Duke University, Durham, NC 27708-0287, USA.
Biotechnol Bioeng. 1993 Jan 20;41(2):211-20. doi: 10.1002/bit.260410207.
Differences in plasmid retention and expression are studied in both suspended and biofilm cultures of Escherichia coli DH5alpha(PMJR1750). An alternative mathematical model is proposed which allows the determination of plasmid loss probability in both suspended batch and continuously fed biofilm cultures. In our experiments, the average probability of plasmid loss of E. coli DH5alpha(pMJR1750) is 0.0022 in batch culture in the absence of antibiotic selection pressure and inducer. Under the induction of 0.17 MM IPTG, the maximum growth rate of plasmid-bearing cells in suspended batch culture dropped from 0.45 h(-1) to 0.35 h(-1) and the beta-galactosidase concentration reached an experimental maximum of 0.32. pg/cell 4 hours after the initiation of induction. At both 0.34 and 0.51 mM IPTG, growth rates in batch cultures decreased to 0.16 h(-1), about 36% of that without IPTG, and the beta-galactosidase concentration reached an experimental maximum of 0.47 pg/cell 3 hours after induction.In biofilm cultures, both plasmid-bearing and plasmid-free cells in increase with time reaching a plateau after 96 hours n the absence of both the inducer and any antibiotic selection pressure. Average probability of plasmid loss for biofilm-bound E. coli DH5beta(pMJR1750) population was 0.017 without antibiotic selection. Once the inducer IPTG was added, the concentration of plasmid-bearing cells in biofilm dropped dramatically while plasmid-free cell numbers maintained unaffected. The beta-galactosidase concentration reached a maximum in all biofilm experiments 24 hours after induction; they were 0.08, 0.1, and 0.12 pg/cel under 0.17, 0.34, and 0.51 mM IPTG, respectively.
研究了在大肠杆菌 DH5alpha(PMJR1750)的悬浮和生物膜培养物中质粒的保留和表达差异。提出了一种替代的数学模型,该模型可以确定悬浮分批和连续进料生物膜培养物中质粒丢失的概率。在我们的实验中,在不存在抗生素选择压力和诱导剂的情况下,大肠杆菌 DH5alpha(pMJR1750)的质粒丢失的平均概率为 0.0022 在分批培养中。在 0.17 mM IPTG 的诱导下,带有质粒的细胞在悬浮分批培养中的最大生长速率从 0.45 h(-1)下降到 0.35 h(-1),β-半乳糖苷酶浓度在诱导开始后 4 小时达到实验最大值 0.32 pg/细胞。在 0.34 和 0.51 mM IPTG 下,分批培养物中的生长速率均下降至 0.16 h(-1),约为无 IPTG 时的 36%,β-半乳糖苷酶浓度在诱导后 3 小时达到实验最大值 0.47 pg/细胞。在生物膜培养物中,带有质粒和无质粒的细胞都随时间增加,在没有诱导剂和任何抗生素选择压力的情况下,96 小时后达到平台期。在没有抗生素选择的情况下,生物膜结合的大肠杆菌 DH5beta(pMJR1750)群体的质粒丢失平均概率为 0.017。一旦加入诱导剂 IPTG,生物膜中带有质粒的细胞浓度急剧下降,而无质粒细胞数量保持不变。所有生物膜实验中的β-半乳糖苷酶浓度在诱导后 24 小时达到最大值;在 0.17、0.34 和 0.51 mM IPTG 下,它们分别为 0.08、0.1 和 0.12 pg/细胞。