Kang R-J, Shi D-J, Cong W, Cai Z-L, Ouyang F
State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, China.
J Appl Microbiol. 2005;98(3):693-8. doi: 10.1111/j.1365-2672.2004.02510.x.
The aim of the present investigation was to study the effects of different inorganic carbon and nitrogen sources on nitrate uptake and heterocyst differentiation in the culture of cyanobacterium Anabaena sp. PCC 7120.
Anabaena was cultivated in media BG11 containing combined nitrogen and supplementary NaHCO3 or CO2. Cell growth, heterocyst differentiation, nitrate reductase (NR, EC 1.7.7.2), glucose-6-phosphate dehydrogenase (G6PDH, EC 1.1.1.49) and NO uptake were analysed. The cells cultivated in BG11(0) medium with aeration were taken as reference. Experimental results showed that the differentiation frequency of heterocysts when the cells were cultivated with elevated CO2 was higher than that of the cells grown with air or bicarbonate. Heterocysts appeared unexpectedly when CO2 was introduced into the medium containing nitrate. However, no heterocysts emerged when CO2 was added to medium containing NH or urea, or when NaHCO3 was supplied to the medium with nitrate. Both nitrate uptake rate and nitrate reduction enzyme activity were depressed by the supplement of CO2 to the culture. The activity of G6PDH was enhanced with the increase in heterocyst differentiation frequency.
CO2 might compete with NO for energy and electrons in the uptake process and CO2 appears favoured. This led to a high intracellular C/N ratio and a relative N limitation. So the process of heterocyst differentiation was activated to supplement nitrogen uptake.
This study provided an attractive possibility to form more heterocysts by rapid growth of Anabaena cells cultivated in the medium containing nitrate in order to increase nitrogen fixation and hydrogen production.
本研究旨在探讨不同无机碳源和氮源对蓝藻鱼腥藻PCC 7120培养过程中硝酸盐吸收和异形胞分化的影响。
将鱼腥藻培养于含有化合态氮并补充了NaHCO₃或CO₂的BG11培养基中。分析细胞生长、异形胞分化、硝酸还原酶(NR,EC 1.7.7.2)、葡萄糖-6-磷酸脱氢酶(G6PDH,EC 1.1.1.49)以及NO吸收情况。以在通气的BG11(0)培养基中培养的细胞作为对照。实验结果表明,在高浓度CO₂条件下培养的细胞异形胞分化频率高于在空气或碳酸氢盐条件下生长的细胞。当向含有硝酸盐的培养基中通入CO₂时,意外出现了异形胞。然而,当向含有NH₄⁺或尿素的培养基中添加CO₂时,或者向含有硝酸盐的培养基中供应NaHCO₃时,均未出现异形胞。向培养物中补充CO₂会抑制硝酸盐吸收速率和硝酸还原酶活性。G6PDH的活性随着异形胞分化频率的增加而增强。
在吸收过程中,CO₂可能与NO竞争能量和电子,且似乎更占优势。这导致细胞内C/N比升高以及相对的氮限制。因此,异形胞分化过程被激活以补充氮的吸收。
本研究提供了一种诱人的可能性,即通过在含有硝酸盐的培养基中快速培养鱼腥藻细胞来形成更多异形胞,从而增加固氮和产氢量。