Pressure effects on the abiotic polymerization of glycine

被引:39
作者
Ohara, Shohei
Kakegawa, Takeshi
Nakazawa, Hiromoto
机构
[1] Tohoku Univ, Grad Sch Sci, Dept Earth & Planetary Mat Sci, Sendai, Miyagi 9808952, Japan
[2] Natl Inst Mat Sci, Tsukuba, Ibaraki 3050044, Japan
来源
ORIGINS OF LIFE AND EVOLUTION OF BIOSPHERES | 2007年 / 37卷 / 03期
基金
日本学术振兴会;
关键词
deep sediment; diagenesis; glycine; high pressure; LC/MS; peptide; polymerization; pre-biotic molecular evolution;
D O I
10.1007/s11084-007-9067-4
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polymerization experiments were performed using dry glycine under various pressures of 5-100 MPa at 150 degrees C for 1-32 days. The series of experiments was carried out under the assumption that the pore space of deep sediments was adequate for dehydration polymerization of pre-biotic molecules. The products show various colors ranging from dark brown to light yellow, depending on the pressure. Visible and infrared spectroscopy reveal that the coloring is the result of formation of melanoidins at lower pressures. High-performance liquid chromatography and mass spectrometry analyses of the products show that: (1) glycine in all the experimental runs oligomerizes from 2-mer to 10-mer; (2) the yields are dependent on pressure up to 25 MPa and decrease slightly thereafter; and (3) polymerization progressed for the first 8 days, while the amounts of oligomers remained constant for longer-duration runs of up to 32 days. These results suggest that pressure inhibits the decomposition of amino acids and encourages polymerization in the absence of a catalyst. Our results further imply that abiotic polymerization could have occurred during diagenesis in deep sediments rather than in oceans.
引用
收藏
页码:215 / 223
页数:9
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