Castet J C, Craynest M, Barbotin J N, Truffaut N
Laboratoire de Technologie Enzymatique, URA CNRS 1442, Université de Technologie de Compiègne, France.
FEMS Microbiol Rev. 1994 May;14(1):63-7. doi: 10.1111/j.1574-6976.1994.tb00074.x.
The immobilization of recombinant Bacillus subtilis in K-carrageenan gel beads has been performed in order to study the growth conditions inside the gel beads and to improve plasmid stability. Bacterial colonies showing high cell density were studied using scanning electron microscopy. A series of continuous cultures of free and immobilized B. subtilis MT119 (pHV1431, pIL252 and pIL252 Kpn) have been developed without selection pressure. In the free-cell systems, it was found that a loss of plasmid vectors occurred after a short period. In contrast, in the immobilized cell systems, plasmid-free segregants were not detected in any of the cases during the first 80 h of the culture.
为了研究卡拉胶凝胶珠内的生长条件并提高质粒稳定性,已将重组枯草芽孢杆菌固定在卡拉胶凝胶珠中。使用扫描电子显微镜研究了显示高细胞密度的细菌菌落。在没有选择压力的情况下,已开展了一系列游离和固定化枯草芽孢杆菌MT119(pHV1431、pIL252和pIL252 Kpn)的连续培养。在游离细胞系统中,发现质粒载体在短时间后发生丢失。相比之下,在固定化细胞系统中,在培养的前80小时内,任何情况下均未检测到无质粒的分离物。