Persson A, Molin G, Andersson N, Sjöholm J
Department of Applied Microbiology, Chemical Center, Lund University, S-221 00 Lund, Sweden.
Biotechnol Bioeng. 1990 Jul;36(3):252-5. doi: 10.1002/bit.260360306.
Production of biosurfactant AP-6 and consumption of carbon (succinic acid) and nitrogen (ammonium ions) by Pseudomonas fluorescens 378 were studied under different growth conditions. The study was performed in a microcomputer controlled multibatch fermentation system which enabled simultaneous running of 10 fermentors. The fermentors were mantled glass vessels, temperature controlled by circulated water, and mixing was arranged by magnetic stirrers. They were connected to the computer system (pH measurement and control) via signal conditioning cards. The microcomputer had a 128 kbytes RAM, two 800-kbyte floppy disc drives, a graphic terminal, and expansion cards. Biosurfactant production was independent of the carbon-to-nitrogen ratio and the phosphorus content in the medium. Omitting the Fe(III) supplement to the medium increased the product yield by 120%. Changes in oxygen transfer rate and pH in the iron deficient cultures did not have any effect on the product yield. Iron deficiency increased the cell consumption of carbon source. Consumption of carbon source in relation to nitrogen uptake (carbon/nitrogen quotient) increased with increasing quotient in the growth medium. The uptake of carbon and nitrogen changed in the intervals of 1.2-1.5 g/g biomass and 0.09-0.16 g/g biomass, respectively. The consumption of carbon increased from 1.5 g/g biomass to 2.0 g/g biomass when the medium concentration of phosphorus was decreased from 0.18 to 0.027 g/L.
在不同生长条件下,研究了荧光假单胞菌378合成生物表面活性剂AP - 6以及对碳源(琥珀酸)和氮源(铵离子)的消耗情况。该研究在一个由微型计算机控制的多批次发酵系统中进行,该系统能够同时运行10个发酵罐。发酵罐为带夹套的玻璃容器,通过循环水控制温度,用磁力搅拌器进行搅拌。它们通过信号调节卡连接到计算机系统(用于pH测量和控制)。微型计算机有128千字节的随机存取存储器、两个800千字节的软盘驱动器、一个图形终端和扩展卡。生物表面活性剂的合成与培养基中的碳氮比和磷含量无关。培养基中不添加Fe(III)可使产物产量提高120%。缺铁培养物中氧传递速率和pH的变化对产物产量没有任何影响。缺铁增加了细胞对碳源的消耗。相对于氮吸收量(碳/氮商)的碳源消耗量随着生长培养基中该商值的增加而增加。碳和氮的吸收量分别在1.2 - 1.5克/克生物量和0.09 - 0.16克/克生物量的范围内变化。当培养基中磷浓度从0.18克/升降至0.027克/升时,碳的消耗量从1.5克/克生物量增加到2.0克/克生物量。