Lee S Y, Mermelstein L D, Papoutsakis E T
BioProcess Engineering Research Center, Korea Advanced Institute of Science and Technology, Taejon.
FEMS Microbiol Lett. 1993 Apr 15;108(3):319-23. doi: 10.1111/j.1574-6968.1993.tb06122.x.
The copy number and stability of several plasmid vectors in Clostridium acetobutylicum ATCC 824 were determined. The protocols were modified from the traditional ones to overcome the problems associated with unusual behavior of C. acetobutylicum cells on solid medium. The plasmid copy numbers of pSYL2, pFNK1, pFNK3, and pFNK5 in strain ATCC 824 were 14, 8, 6, and 6, respectively. pSYL2 and pFNK1 were segregationally stable, since the fractions of plasmid-carrying cells after 60 generations of growth without antibiotic (erythromycin) were 73% and 77%, respectively. Vector pFNK1 carrying fermentative genes was found to be rather unstable. The observed instability seemed to be due to the complex host-plasmid interactions by amplified expression of enzymes involved in the tightly regulated primary metabolism of C. acetobutylicum.
测定了几种质粒载体在丙酮丁醇梭菌ATCC 824中的拷贝数和稳定性。对实验方案进行了改进,以克服与丙酮丁醇梭菌细胞在固体培养基上异常行为相关的问题。菌株ATCC 824中pSYL2、pFNK1、pFNK3和pFNK5的质粒拷贝数分别为14、8、6和6。pSYL2和pFNK1在分离时是稳定的,因为在无抗生素(红霉素)的情况下生长60代后,携带质粒的细胞比例分别为73%和77%。发现携带发酵基因的载体pFNK1相当不稳定。观察到的不稳定性似乎是由于丙酮丁醇梭菌严格调控的初级代谢中参与酶的扩增表达导致的复杂宿主 - 质粒相互作用。