Prokhorova L I, Revina A A
Bach Institute of Biochemistry, Russian Academy of Sciences, Moscow, 117071 Russia.
Radiats Biol Radioecol. 2001 Jan-Feb;41(1):24-32.
The present research work was done with the main purpose to study early stages of interaction of carotenoids (Car) with molecular oxygen and clarify their role in the mechanism responsible for Car radiochemical stability and carotenoid ability to decrease concentration of the most active oxygen transients like superoxide anion radicals (O2.-). Alcoholic and phosphate buffer (pH 7.5) solutions of carotenoid fucoxanthin (Fx) were used for investigation of the oxygen effect on the absorption spectra in the UV-Visible range. Special analysis of time dependent reversible shifts of absorption bands of evacuated Fx solution after contact with O2 indicated existence of equilibrium between two distinct forms of Car: Fx and the labile charge transfer complex (Fx+delta...O2-delta). The velocity of the achievement of equilibrium state and a degree of reversibility depend on chemical structure of the carotenoid, oxygen content and the solvent nature. Radiation-chemical methods were used to confirm the important role of primary Car oxocomplexes in different redox processes. It appeared that the yield of radiation-chemical bleaching of Fx, G-Fx, is 0.02-0.05 molecule/100 eV in the presence of oxygen, which in hundred times less the yield achieved in anaerobic conditions. The obtained results provide the evidence of Fx high level of stability under radiation, and demonstrate the supreme importance of reversible oxocomplex (Fx+delta...O2-delta) in stabilizing carotenoids in aerobic medium. The pulse radiolysis method with spectrophotometric registration of transients was used for generation and studying of mechanism O2.- interaction with different carotenoids. Introduction of any carotenoids containing oxygen (10(-5) M) in phosphate buffer solutions (pH 7.5) caused a red-shift of absorption maximum (from 5 to 15 nm) and difference in kinetics of O2.- decay. These results prove that radiation generated esolv- are directly accepted by (Car...O2) with consequent formation of superoxocomplexes (Car...O2.-) instead of O2.-. On the base of detecting the following transformation of superoxocomplexes the peroxocomplex (Car+...O2(2-)) was identified. In case of Fx a peroxocomplex (Fx+...O2(2-)) had absorption band with lambda max at approximately 360 nm. It is very important to mention that beta-carotene does not cause the similar effect and gets easily oxydized when exposed to the air.
本研究工作的主要目的是研究类胡萝卜素(Car)与分子氧相互作用的早期阶段,并阐明它们在类胡萝卜素放射化学稳定性机制以及类胡萝卜素降低最活泼的氧瞬变体如超氧阴离子自由基(O2.-)浓度能力方面的作用。使用类胡萝卜素岩藻黄质(Fx)的乙醇溶液和磷酸盐缓冲液(pH 7.5)来研究氧对紫外-可见范围内吸收光谱的影响。对抽空的Fx溶液与O2接触后吸收带随时间的可逆位移进行的特殊分析表明,类胡萝卜素存在两种不同形式之间的平衡:Fx和不稳定的电荷转移络合物(Fx+δ...O2-δ)。达到平衡状态的速度和可逆程度取决于类胡萝卜素的化学结构、氧含量和溶剂性质。采用辐射化学方法来证实初级类胡萝卜素氧化络合物在不同氧化还原过程中的重要作用。结果表明,在有氧存在的情况下,Fx的辐射化学漂白产率G-Fx为0.02-0.05分子/100 eV,这比在厌氧条件下获得的产率低百倍。所得结果证明了Fx在辐射下具有高度稳定性,并证明了可逆氧化络合物(Fx+δ...O2-δ)在稳定需氧介质中的类胡萝卜素方面的至关重要性。采用瞬态分光光度记录的脉冲辐解方法来产生和研究O2.-与不同类胡萝卜素的相互作用机制。在磷酸盐缓冲溶液(pH 7.5)中引入任何含氧类胡萝卜素(10(-5) M)都会导致吸收最大值发生红移(从5到15 nm)以及O2.-衰减动力学的差异。这些结果证明,辐射产生的值直接被(Car...O2)接受,随后形成超氧络合物(Car...O2.-)而不是O2.-。基于检测到超氧络合物的后续转化,鉴定出了过氧络合物(Car+...O2(2-))。就Fx而言,过氧络合物(Fx+...O2(2-))在约360 nm处有吸收带。非常重要的是要提到,β-胡萝卜素不会产生类似的效果,并且暴露在空气中时很容易被氧化。