Kunz D A, Chen J L, Pan G
Department of Biological Sciences, University of North Texas, Denton, Texas 76203, USA.
Appl Environ Microbiol. 1998 Nov;64(11):4452-9. doi: 10.1128/AEM.64.11.4452-4459.1998.
Pyruvate (Pyr) and alpha-ketoglutarate (alphaKg) accumulated when cells of Pseudomonas fluorescens NCIMB 11764 were cultivated on growth-limiting amounts of ammonia or cyanide and were shown to be responsible for the nonenzymatic removal of cyanide from culture fluids as previously reported (J.-L. Chen and D. A. Kunz, FEMS Microbiol. Lett. 156:61-67, 1997). The accumulation of keto acids in the medium paralleled the increase in cyanide-removing activity, with maximal activity (760 micromol of cyanide removed min-1 ml of culture fluid-1) being recovered after 72 h of cultivation, at which time the keto acid concentration was 23 mM. The reaction products that formed between the biologically formed keto acids and cyanide were unambiguously identified as the corresponding cyanohydrins by 13C nuclear magnetic resonance spectroscopy. Both the Pyr and alpha-Kg cyanohydrins were further metabolized by cell extracts and served also as nitrogenous growth substrates. Radiotracer experiments showed that CO2 (and NH3) were formed as enzymatic conversion products, with the keto acid being regenerated as a coproduct. Evidence that the enzyme responsible for cyanohydrin conversion is cyanide oxygenase, which was shown previously to be required for cyanide utilization, is based on results showing that (i) conversion occurred only when extracts were induced for the enzyme, (ii) conversion was oxygen and reduced-pyridine nucleotide dependent, and (iii) a mutant strain defective in the enzyme was unable to grow when it was provided with the cyanohydrins as a growth substrate. Pyr and alphaKg were further shown to protect cells from cyanide poisoning, and excretion of the two was directly linked to utilization of cyanide as a growth substrate. The results provide the basis for a new mechanism of cyanide detoxification and assimilation in which keto acids play an essential role.
当荧光假单胞菌NCIMB 11764的细胞在氨或氰化物含量限制生长的条件下培养时,丙酮酸(Pyr)和α-酮戊二酸(αKg)会积累,如先前报道(J.-L. Chen和D. A. Kunz,《FEMS微生物学快报》156:61 - 67,1997),它们负责从培养液中以非酶方式去除氰化物。培养基中酮酸的积累与氰化物去除活性的增加平行,培养72小时后可回收最大活性(每毫升培养液每分钟去除760微摩尔氰化物),此时酮酸浓度为23 mM。通过13C核磁共振光谱明确鉴定出生物形成的酮酸与氰化物之间形成的反应产物为相应的氰醇。Pyr和α-Kg氰醇均被细胞提取物进一步代谢,并且还用作含氮生长底物。放射性示踪实验表明,二氧化碳(和氨)作为酶促转化产物形成,酮酸作为副产物再生。负责氰醇转化的酶是氰化物加氧酶,先前已证明其是利用氰化物所必需的,这一证据基于以下结果:(i)仅当提取物诱导产生该酶时才发生转化;(ii)转化依赖于氧气和还原型吡啶核苷酸;(iii)该酶有缺陷的突变菌株在以氰醇作为生长底物时无法生长。进一步表明,Pyr和αKg可保护细胞免受氰化物中毒,并且二者的排泄与将氰化物用作生长底物直接相关。这些结果为酮酸发挥重要作用的氰化物解毒和同化新机制提供了基础。