OBTAINING NUCLEIC ACID PREPARATIONS AND THEIR HYDROLYSATES FROM BIOMASS OF METHANE-OXIDIZING BACTERIA

A. Krasnoshtanova, E. Borovkova
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Abstract

"Due to the unfavourable environmental, social and economic situation, the need for the treatment of oncological diseases and diseases associated with impaired activity of the immune system is increasing. A lot of these drugs are made on the basis of nucleic acid components, the industrial production of which is practically non-existent in Russia. Therefore, a task of current interest is to develop the basis of the technology for obtaining components of nucleic acids, which can be widely used in medicine as immunomodulatory, wound-healing, antiviral, and diagnostic medicine, as well as for cancer treatment. Most of the described in literature methods of isolating nucleic acid components from plant, animal and microbial raw materials are based on the use of toxic and expensive organic solvents, that’s why it is impossible to apply these methods outside of laboratory conditions. The most promising source of raw materials for nucleic acids is the biomass of microorganisms (yeast and bacteria) from biomass, since the use of such source makes it possible to quickly obtain a large enough amount of biomass, and, consequently, a larger amount of nucleic acids. This allows obtaining DNA in addition to RNA. RNA and DNA substances can be used to obtain nucleosides and nitrogenous bases, which are also widely used in medicine. The purpose of these studies was to select the conditions for the extraction of RNA and DNA from the biomass of methane-oxidizing bacteria in one technological cycle, as well as to compare the efficiency of alkaline and acid hydrolysis of microbial RNA and DNA. The need for a two-stage extraction of nucleic acids from the biomass of methane-oxidizing bacteria in order to separately extract RNA and DNA was Substantiated. It was ascertained that at the first stage of extraction at a temperature of 90 ° C, pH 9.0 for 90 min, at least 85% of RNA is extracted. After the separation of the extract by centrifugation, the partially denuclearized biomass must be re-processed under the same conditions in order to extract DNA by at least 83%. The modes of concentration of RNA and DNA solutions by ultrafiltration were selected. It was found that in order to achieve effective deposition of nucleic acids at the isoelectric point, the concentration of the RNA solution must be carried out on the UPM-10 membrane at the concentration degree of 7, and the DNA solution on the UPM-100 membrane at the concentration degree 6. The dynamics of decomposition of nucleic-protein complexes in the medium of monoammonium phosphate was investigated. It was shown that the transition of NA into solution by at least 80% is achieved at a monoammonium phosphate concentration of 1.7 M, a temperature of 55 ° C for 90 min. The use of 5-fold washing of oligonucleotide substances with acidified water (pH 2.0) to remove excess mineral impurities was substantiated. А comparative assessment of acid and alkaline hydrolysis of RNA and DNA was carried out in order to obtain derivatives of nucleic acids."
从甲烷氧化菌生物量中获得核酸制剂及其水解物
“由于不利的环境、社会和经济状况,对肿瘤疾病和与免疫系统活动受损有关的疾病的治疗需求正在增加。这些药物中有很多是由核酸成分制成的,而这种成分在俄罗斯几乎不存在工业化生产。因此,当前的一个重要任务是开发核酸成分提取技术的基础,使其广泛应用于免疫调节、伤口愈合、抗病毒、诊断医学以及癌症治疗等医学领域。文献中所描述的从植物、动物和微生物原料中分离核酸组分的方法大多是基于使用有毒且昂贵的有机溶剂,这就是为什么这些方法不可能在实验室条件之外应用。最有希望的核酸原料来源是来自生物质的微生物(酵母和细菌)的生物质,因为使用这种来源可以快速获得足够多的生物质,从而获得更大量的核酸。这使得除了RNA之外,还可以获得DNA。RNA和DNA物质可以用来获得核苷和含氮碱基,在医学上也有广泛的应用。本研究的目的是选择在一个工艺周期内从甲烷氧化菌生物量中提取RNA和DNA的条件,并比较微生物RNA和DNA的碱性和酸性水解效率。证实了从甲烷氧化菌生物量中提取核酸以分别提取RNA和DNA的必要性。结果表明,在90℃,pH 9.0, 90 min的条件下,第一步提取,至少85%的RNA被提取。在离心分离萃取物后,部分去核的生物质必须在相同条件下重新处理,以提取至少83%的DNA。选择了RNA和DNA溶液的超滤浓缩方式。研究发现,为了在等电点实现核酸的有效沉积,RNA溶液必须在浓度度为7的UPM-10膜上进行浓缩,DNA溶液在浓度度为6的UPM-100膜上进行浓缩。研究了磷酸一铵介质中核蛋白复合物的分解动力学。结果表明,在磷酸一铵浓度为1.7 M、温度为55℃、时间为90 min的条件下,NA向溶液的转变率至少达到80%。用酸化水(pH 2.0)对寡核苷酸物质进行5次洗涤,以去除多余的矿物杂质。А为了获得核酸衍生物,我们对RNA和DNA的酸和碱水解进行了比较评估。”
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