Sotnikov G G
Academy of Sciences, Moscow, USSR.
Life Sci Space Res. 1970;8:90-8.
Iron-porphyrin proteins (catalase, peroxidase, hemoglobin, cytochrome C) represent an important group of redoxenzymes which have vitally important functions in micro-organisms. A biochemiluminescent method was employed for the detection of iron-porphyrin proteins. The reaction of luminol oxidation with H2O2 is accompanied by chemiluminescence. The rate of hydrogen peroxide decomposition increased 10(5)-10(7) -fold in the presence of the above enzymes as compared with ferrous (or ferric) ions. Possible application of this reaction for the detection of iron-porphyrin proteins of microbial origin was studied. Other authors have suggested this reaction for the detection of extraterrestrial life. Kinetics of the above reaction in the presence of iron-porphyrin proteins were shown to differ both in amplitude and duration of the signal from the pattern observed in the presence of non-hemin catalysts. The reaction pattern in the presence of mixed-soil populations is similar to those observed with pure bacterial cultures and individual iron-porphyrin proteins. Photometric tests revealed that among preparations studied the addition of 0.01% lysozyme was the most effective in destroying cell walls in microbial populations. However, removal of cell walls is not a necessary prerequisite for the detection of iron porphyrin since, for effective luminol oxidation with H2O2 the medium should be kept at pH 12.0. Pretreatment of microbial suspensions with ultrasound increased 2-fold the total signal due to iron porphyrins. The above method gives a reproducible signal indicating the presence of iron porphyrins when sterile nutrient media were innoculated with desert soil samples (Repeteck, Kara-Kum) and incubated for 13 hr. The device was able to detect the presence of no less than 10(5) - 10(6) cells per ml. The addition of limonite (Fe2O3 X nH2O) does not result in the appearance of an appreciable signal in the luminol + H2O2 system.
铁卟啉蛋白(过氧化氢酶、过氧化物酶、血红蛋白、细胞色素C)是一类重要的氧化还原酶,在微生物中具有至关重要的功能。采用生物化学发光法检测铁卟啉蛋白。鲁米诺与过氧化氢的氧化反应伴随着化学发光。与亚铁(或铁)离子相比,在上述酶存在的情况下,过氧化氢的分解速率提高了10⁵-10⁷倍。研究了该反应在检测微生物来源的铁卟啉蛋白方面的可能应用。其他作者曾提出该反应可用于检测外星生命。结果表明,在铁卟啉蛋白存在的情况下,上述反应的动力学在信号的幅度和持续时间上均与在非血红素催化剂存在时观察到的模式不同。混合土壤菌群存在时的反应模式与纯细菌培养物和单个铁卟啉蛋白的反应模式相似。光度测试表明,在所研究的制剂中,添加0.01%的溶菌酶对破坏微生物菌群的细胞壁最为有效。然而,去除细胞壁并非检测铁卟啉的必要前提条件,因为要使鲁米诺与过氧化氢发生有效的氧化反应,培养基的pH值应保持在12.0。用超声波对微生物悬浮液进行预处理,可使铁卟啉产生的总信号增加2倍。当用沙漠土壤样本(雷佩捷克、卡拉库姆)接种无菌营养培养基并培养13小时时,上述方法能给出可重复的信号,表明存在铁卟啉。该装置能够检测到每毫升不少于10⁵-10⁶个细胞的存在。添加褐铁矿(Fe₂O₃·nH₂O)不会在鲁米诺+过氧化氢体系中产生明显的信号。