Department of Applied Molecular Biosciences, Graduate School of Bioagricultural Sciences, Nagoya University , Furou-chou, Chikusa, Nagoya, Aichi 464-8601, Japan.
Department of Applied Biological Science, Faculty of Agriculture, Kagawa University , Miki-cho, Kita-gun, Kagawa 761-0795, Japan.
J Agric Food Chem. 2017 Aug 2;65(30):6131-6139. doi: 10.1021/acs.jafc.7b01893. Epub 2017 Jul 24.
Here, we report the occurrence of the (2R,3S)-isomer of 2-amino-3,4-dihydroxybutanoic acid (d-ADHB) in the fruiting body of an edible mushroom, Hypsizygus marmoreus. This is an unusual example of the accumulation of a d-amino acid whose enantiomer is not a proteinogenic amino acid. We show that d-ADHB occurs specifically in the mushroom H. marmoreus. Other edible mushrooms examined, including Pholiota microspora, Pleurotus eryngii, Mycena chlorophos, Sparassis crispa, Grifola frondosa, Pleurotus ostreatus, and Flammulina velutipes, do not contain detectable levels of d-ADHB. The concentration of d-ADHB in the fruiting body of H. marmoreus is relatively high (approximately 1.3 mg/g of fruiting body) and is comparable to the concentration of some of the most abundant free proteinogenic amino acids. Quantitative analysis of d-ADHB during fruiting body development demonstrated that the amino acid is synthesized during the fruiting body formation period. The absence of the putative precursors of d-ADHB, the (2S,3S)-isomer of ADHB and 2-oxo-tetronate, and the enzyme activities of d-ADHB racemase (2-epimerase) and transaminase suggested that d-ADHB is synthesized by a unique mechanism in this organism. Our data also suggested that the lack of or low expression of a d-ADHB degradation enzyme is a key determinant of d-ADHB accumulation in H. marmoreus.
在这里,我们报告了(2R,3S)-2-氨基-3,4-二羟基丁酸(d-ADHB)在食用蘑菇杏鲍菇的子实体中出现。这是一种不寻常的例子,即积累了一种非蛋白质氨基酸的对映异构体。我们表明,d-ADHB 特异性地存在于蘑菇 H. marmoreus 中。其他检查的食用蘑菇,包括 Pholiota microspora、Pleurotus eryngii、Mycena chlorophos、Sparassis crispa、Grifola frondosa、Pleurotus ostreatus 和 Flammulina velutipes,均未检测到 d-ADHB。H. marmoreus 子实体中 d-ADHB 的浓度相对较高(约 1.3mg/g 子实体),与一些最丰富的游离蛋白质氨基酸的浓度相当。在子实体发育过程中对 d-ADHB 的定量分析表明,该氨基酸在子实体形成期间合成。缺乏 d-ADHB 的假定前体(ADHB 的(2S,3S)-异构体和 2-氧代四氢酸盐)以及 d-ADHB 外消旋酶(2-差向异构酶)和转氨酶的酶活性表明,d-ADHB 是由该生物体中的独特机制合成的。我们的数据还表明,缺乏或低表达 d-ADHB 降解酶是 d-ADHB 在 H. marmoreus 中积累的关键决定因素。