利用双歧杆菌细胞粗提物生产乳酸- n -二糖I。

IF 1.2 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal of applied glycoscience Pub Date : 2022-05-25 eCollection Date: 2022-01-01 DOI:10.5458/jag.jag.JAG-2021_0012
Shuntaro Machida, Katsuichi Saito, Mamoru Nishimoto, Motomitsu Kitaoka
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引用次数: 0

摘要

乳酸- n -二糖I (LNB)被认为是人乳寡糖中的双歧因子,可以利用大肠杆菌重组产生的1,3-β-半乳糖- n -乙酰己糖胺磷酸化酶、蔗糖磷酸化酶、葡萄糖-己糖- 1-磷酸尿苷基转移酶和葡萄糖- 4-聚甲酰基酶四种双歧杆菌酶从蔗糖和葡萄糖nac中实际生产。本文报道了用相同的酶法生产LNB,而不使用转基因酶来考虑将LNB用于食品成分。这四种酶均作为双歧杆菌胞内酶产生。粗提物的混合物中含有所有四种酶,其他酶干扰LNB的产生,即磷酸葡萄糖葡萄糖化酶、果糖6-磷酸磷酸酮醇酶和糖原磷酸化酶。前两种干扰酶在胰酶存在下,通过47°C热处理1小时选择性失活,糖原磷酸化酶通过葡萄糖淀粉酶水解其可能的受体分子而失活。最后,在含有300 mM GlcNAc的100 ml反应混合物中,91%的GlcNAc转化为LNB。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Production of Lacto-<i>N</i>-biose I Using Crude Extracts of Bifidobacterial Cells.

Production of Lacto-<i>N</i>-biose I Using Crude Extracts of Bifidobacterial Cells.

Production of Lacto-<i>N</i>-biose I Using Crude Extracts of Bifidobacterial Cells.

Production of Lacto-N-biose I Using Crude Extracts of Bifidobacterial Cells.

Lacto-N-biose I (LNB) is supposed to represent the bifidus factor in human milk oligosaccharides, and can be practically produced from sucrose and GlcNAc using four bifidobacterial enzymes, 1,3-β-galactosyl-N-acetylhexosamine phosphorylase, sucrose phosphorylase, UDP-glucose-hexose 1-phosphate uridylyltransferase, and UDP-glucose 4-epimerase, recombinantly produced by Escherichia coli. Here the production of LNB by the same enzymatic method without using genetically modified enzymes to consider the use of LNB for a food ingredient was reported. All four enzymes were produced as the intracellular enzymes of Bifidobacterium strains. The mixture of the crude extracts contained all four enzymes, with other enzymes interfering with the LNB production, namely, phosphoglucomutase, fructose 6-phosphate phosphoketolase, and glycogen phosphorylase. The first two interfering enzymes were selectively inactivated by heat treatment at 47 °C for 1 h in the presence of pancreatin, and glycogen phosphorylase was disabled by hydrolyzing its possible acceptor molecules using glucoamylase. Finally, 91 % of GlcNAc was converted into LNB in the 100-mL reaction mixture containing 300 mM GlcNAc.

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来源期刊
Journal of applied glycoscience
Journal of applied glycoscience BIOCHEMISTRY & MOLECULAR BIOLOGY-
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