Biomedical Sciences Division, Lawarence Livermore National Laboratory, University of California, Livermore, California 94550, USA.
Biotechnol Bioeng. 1992 Sep;40(6):705-12. doi: 10.1002/bit.260400609.
Continous culture experiments with the obligatory methanotroph, Methylosinus trichosporium OB3b, were conducted to study the whole-cell methane monooxygenase (MMO) and nitrogenase activities in a nitrate minimal salts medium under oxygen-limited conditions with methane as the carbone source. The important variables investigated were the feed medium concentrations of copper and nitrate, CO(2) addition, the agitation speed, and the dilution rate. M. trichosporium OB3b required quantitative amounts of copper (2.6 x 10(-4) g Cu/g dry cell Wt) for the exclusive production of particulate MMo during continuous culture growth. When the feed medium nitrate concentration was varied in the range of 5-50 mM, the whole-cell specific pMMO activity exhibited a maximum at 40 mM. The elimination of external CO(2) gassing decreased pMMO activity by more than 30%. The steady-state cell density increased continuously over a 300-700 rpm range of agitation speed, whereas, the pMMO activity became maximal at 400 rpm. Also, the pMMO activity increased with the dilution rate up to 0.06 h(-1) and remained constant thereafter. Maximal continuous pMMO productivity was, thus, achieved in Higgin's medium containing 10 microM Cu, 80 microM Fe, and 40 mM nitrate with an agitation speed of 500 rpm and a dilution rate of 0.06 h(-1). Nitrogenase activity, on the other hand, increased over a feed medium copper concentration of 2-15 microM, falling sharply at 20 microM, and it exhibited a minimum at 20 mM when the feed medium nitrate concentration was varied.
连续培养严格依赖甲烷的甲烷氧化菌(Methylosinus trichosporium OB3b),在以甲烷为碳源、氧限制条件下、硝酸盐最小盐培养基中,研究整个细胞甲烷单加氧酶(MMO)和固氮酶活性。考察的重要变量是铜和硝酸盐的进料介质浓度、CO(2)添加、搅拌速度和稀释率。OB3b 需要定量的铜(2.6 x 10(-4) g Cu/g 干细胞重量)才能在连续培养生长过程中专门产生颗粒状 MMo。当进料介质硝酸盐浓度在 5-50 mM 范围内变化时,整个细胞比 pMMO 活性在 40 mM 时达到最大值。消除外部 CO(2)通气会使 pMMO 活性降低超过 30%。在 300-700 rpm 的搅拌速度范围内,稳态细胞密度持续增加,而 pMMO 活性在 400 rpm 时达到最大值。此外,pMMO 活性随着稀释率的增加而增加,直到 0.06 h(-1),此后保持不变。因此,在含有 10 microM Cu、80 microM Fe 和 40 mM 硝酸盐的 Higgin 培养基中,以 500 rpm 的搅拌速度和 0.06 h(-1)的稀释率实现了最大的连续 pMMO 生产力。另一方面,固氮酶活性随着进料介质铜浓度在 2-15 microM 之间增加,在 20 microM 时急剧下降,当进料介质硝酸盐浓度变化时,在 20 mM 时达到最小值。