Olsson L, Larsen M E, Rønnow B, Mikkelsen J D, Nielsen J
Department of Biotechnology, Technical University of Denmark, Lyngby, Denmark.
Appl Environ Microbiol. 1997 Jun;63(6):2366-71. doi: 10.1128/aem.63.6.2366-2371.1997.
Silencing of MIG1, a transcription factor imposing carbon catabolite repression on invertase, was attempted, either by disrupting the gene or by expressing antisense copies of the gene. The performance of the recombinant strains in bioreactor batch cultivations on sucrose, in the presence of glucose, was compared with that of the wild-type strain under the same conditions. In the delta migI strain, the rate of sucrose utilization was independent (10 mmol/g/h) of the glucose concentration. During the cultivations with the wild-type strain and the antisense strains, two distinct phases were observed. The rates of sucrose hydrolysis were < 1 mmol/g/h and 9 to 10 mmol/g/h in the first and second phases, respectively. Entry into the second cultivation phase was characterized by a decline in glucose concentration below 12 mmol/liter. As expected, disruption of MIG1 resulted in a relief of glucose repression. However, silencing of MIG1 expression was not achieved by expressing antisense MIG1, even though antisense MIG1 RNA was sufficiently stable to be detected. In the wild-type and delta migI strains, the specific growth rate was 0.32 to 0.33 h-1, whereas it was lower in the antisense strains, 0.25 to 0.30 h-1.
尝试通过破坏基因或表达该基因的反义拷贝来沉默MIG1(一种对转化酶施加碳分解代谢物阻遏作用的转录因子)。在相同条件下,将重组菌株在有葡萄糖存在的情况下于生物反应器分批培养中利用蔗糖的性能与野生型菌株进行了比较。在缺失migI基因的菌株中,蔗糖利用速率与葡萄糖浓度无关(10 mmol/g/h)。在用野生型菌株和反义菌株进行培养的过程中,观察到了两个不同的阶段。在第一阶段和第二阶段,蔗糖水解速率分别<1 mmol/g/h和9至10 mmol/g/h。进入第二培养阶段的特征是葡萄糖浓度降至12 mmol/L以下。正如预期的那样,MIG1的破坏导致葡萄糖阻遏的解除。然而,即使反义MIG1 RNA足够稳定可被检测到,通过表达反义MIG1也未实现MIG1表达的沉默。在野生型和缺失migI基因的菌株中,比生长速率为0.32至0.33 h-1,而在反义菌株中较低,为0.25至0.30 h-1。