Department of Applied Science, Brookhaven National Laboratory, Upton, New York 11973.
Appl Environ Microbiol. 1993 Jan;59(1):109-13. doi: 10.1128/aem.59.1.109-113.1993.
The biodegradation of iron-citrate complexes depends on the structure of the complex formed between the metal and citric acid. Ferric iron formed a bidentate complex with citric acid, [Fe(III) (OH)(2) cit] involving two carboxylic acid groups, and was degraded at the rate of 86 muM h. In contrast, ferrous iron formed a tridentate complex with citric acid, [Fe(II) cit], involving two carboxylic acid groups and the hydroxyl group, and was resistant to biodegradation. However, oxidation and hydrolysis of the ferrous iron resulted in the formation of a tridentate ferric-citrate complex, [Fe(III)OH cit], which was further hydrolyzed to a bidentate complex, [Fe(III)(OH)(2) cit], that was readily degraded. The rate of degradation of the ferrous-citrate complex depended on the rate of its conversion to the more hydrolyzed form of the ferric-citrate complex. Bacteria accelerated the conversion much more than did chemical oxidation and hydrolysis.
柠檬酸铁复合物的生物降解取决于金属和柠檬酸形成的复合物的结构。三价铁与柠檬酸形成双齿络合物[Fe(III)(OH)(2)cit],涉及两个羧酸基团,以 86 μM h 的速率降解。相比之下,二价铁与柠檬酸形成三齿络合物[Fe(II)cit],涉及两个羧酸基团和羟基,并且不易生物降解。然而,二价铁的氧化和水解导致形成三齿铁-柠檬酸络合物[Fe(III)OH cit],它进一步水解为双齿络合物[Fe(III)(OH)(2)cit],容易降解。亚铁-柠檬酸络合物的降解速率取决于其转化为更易水解的铁-柠檬酸络合物的速率。细菌的转化速度比化学氧化和水解快得多。