S. But, R. Z. Suleimanov, I. Y. Oshkin, O. Rozova, I. Mustakhimov, Nikolai V. Pimenov, S. Dedysh, V. Khmelenina
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To obtain glycogen-free cell biomass of this methanotroph, glycogen synthase mutants, ΔglgA1, ΔglgA2, and ΔglgA1ΔglgA2, were constructed. The mutant lacking both glycogen synthases exhibited a glycogen-deficient phenotype, whereas the intracellular glycogen content was not reduced in strains defective in either GlgA1 or GlgA2, thus suggesting functional redundancy of these enzymes. Inactivation of the glk gene encoding glucokinase also resulted in a sharp decrease in glycogen content and accumulation of free glucose in cells. Wild-type strain MIR and the mutant strain ΔglgA1ΔglgA2 were also grown in a bioreactor operated in batch and continuous modes. Cell biomass of ΔglgA1ΔglgA2 mutant obtained during batch cultivation displayed high protein content (71% of dry cell weight (DCW) compared to 54% DCW in wild-type strain) as well as a strong reduction in glycogen content (10.8 mg/g DCW compared to 187.5 mg/g DCW in wild-type strain). The difference in protein and glycogen contents in biomass of these strains produced during continuous cultivation was less pronounced, yet biomass characteristics relevant to SCP production were slightly better for ΔglgA1ΔglgA2 mutant. Genome analysis revealed the presence of glgA1-like genes in all methanotrophs of the Gammaproteobacteria and Verrucomicrobia, while only a very few methanotrophic representatives of the Alphaproteobacteria possessed these determinants of glycogen biosynthesis. The glgA2-like genes were present only in genomes of gammaproteobacterial methanotrophs with predominantly halo- and thermotolerant phenotypes. 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Wild-type strain MIR and the mutant strain ΔglgA1ΔglgA2 were also grown in a bioreactor operated in batch and continuous modes. Cell biomass of ΔglgA1ΔglgA2 mutant obtained during batch cultivation displayed high protein content (71% of dry cell weight (DCW) compared to 54% DCW in wild-type strain) as well as a strong reduction in glycogen content (10.8 mg/g DCW compared to 187.5 mg/g DCW in wild-type strain). The difference in protein and glycogen contents in biomass of these strains produced during continuous cultivation was less pronounced, yet biomass characteristics relevant to SCP production were slightly better for ΔglgA1ΔglgA2 mutant. Genome analysis revealed the presence of glgA1-like genes in all methanotrophs of the Gammaproteobacteria and Verrucomicrobia, while only a very few methanotrophic representatives of the Alphaproteobacteria possessed these determinants of glycogen biosynthesis. 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引用次数: 0
摘要
将甲烷转化为单细胞蛋白(SCP)的生物技术意味着要使用快速生长的耐高温好氧甲烷营养细菌。其中,甲基球菌属(Methylococcus)的成员受到了大量研究的关注,并被用于商业工厂的运营。荚膜甲基球菌 MIR 是最近发现的该属的一个成员,有可能用于生产 SCP。与其他甲基球菌一样,这种细菌以糖原的形式储存碳和能量,尤其是在氮限制条件下生长时。菌株 MIR 的基因组编码两种糖原合成酶,即 GlgA1 和 GlgA2,它们之间的亲缘关系一般。为了获得这种甲烷营养体的无糖原细胞生物量,构建了糖原合成酶突变体,即ΔglgA1、ΔglgA2和ΔglgA1ΔglgA2。缺乏这两种糖原合成酶的突变体表现出糖原缺乏的表型,而 GlgA1 或 GlgA2 均有缺陷的菌株细胞内糖原含量并不减少,因此表明这些酶存在功能冗余。编码葡萄糖激酶的 glk 基因失活也会导致糖原含量急剧下降和细胞内游离葡萄糖的积累。野生型菌株 MIR 和突变型菌株 ΔglgA1ΔglgA2 也在以间歇和连续模式运行的生物反应器中生长。在批量培养过程中获得的突变株ΔglgA1ΔglgA2的细胞生物量显示出较高的蛋白质含量(占细胞干重(DCW)的71%,而野生型菌株的DCW为54%),以及糖原含量的显著降低(10.8 mg/g DCW,而野生型菌株的DCW为187.5 mg/g)。这些菌株在连续培养过程中产生的生物量中蛋白质和糖原含量的差异不太明显,但ΔglgA1ΔglgA2突变体与SCP生产相关的生物量特征略好。基因组分析表明,在所有产甲烷的加玛蛋白菌和Verrucomicrobia中都存在类似glgA1的基因,而只有极少数产甲烷的阿尔法蛋白菌具有这些糖原生物合成的决定性基因。类似 glgA2 的基因只存在于主要具有耐晕和耐热表型的甘蛋白细菌甲烷营养体的基因组中。讨论了糖原在能量储备方面的作用。
New Solutions in Single-Cell Protein Production from Methane: Construction of Glycogen-Deficient Mutants of Methylococcus capsulatus MIR
The biotechnology of converting methane to single-cell protein (SCP) implies using fast-growing thermotolerant aerobic methanotrophic bacteria. Among the latter, members of the genus Methylococcus received significant research attention and are used in operating commercial plants. Methylococcus capsulatus MIR is a recently discovered member of this genus with the potential to be used for the purpose of SCP production. Like other Methylococcus species, this bacterium stores carbon and energy in the form of glycogen, particularly when grown under nitrogen-limiting conditions. The genome of strain MIR encodes two glycogen synthases, GlgA1 and GlgA2, which are only moderately related to each other. To obtain glycogen-free cell biomass of this methanotroph, glycogen synthase mutants, ΔglgA1, ΔglgA2, and ΔglgA1ΔglgA2, were constructed. The mutant lacking both glycogen synthases exhibited a glycogen-deficient phenotype, whereas the intracellular glycogen content was not reduced in strains defective in either GlgA1 or GlgA2, thus suggesting functional redundancy of these enzymes. Inactivation of the glk gene encoding glucokinase also resulted in a sharp decrease in glycogen content and accumulation of free glucose in cells. Wild-type strain MIR and the mutant strain ΔglgA1ΔglgA2 were also grown in a bioreactor operated in batch and continuous modes. Cell biomass of ΔglgA1ΔglgA2 mutant obtained during batch cultivation displayed high protein content (71% of dry cell weight (DCW) compared to 54% DCW in wild-type strain) as well as a strong reduction in glycogen content (10.8 mg/g DCW compared to 187.5 mg/g DCW in wild-type strain). The difference in protein and glycogen contents in biomass of these strains produced during continuous cultivation was less pronounced, yet biomass characteristics relevant to SCP production were slightly better for ΔglgA1ΔglgA2 mutant. Genome analysis revealed the presence of glgA1-like genes in all methanotrophs of the Gammaproteobacteria and Verrucomicrobia, while only a very few methanotrophic representatives of the Alphaproteobacteria possessed these determinants of glycogen biosynthesis. The glgA2-like genes were present only in genomes of gammaproteobacterial methanotrophs with predominantly halo- and thermotolerant phenotypes. The role of glycogen in terms of energy reserve is discussed.