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甘草细胞培养物中 6'-去氧查尔酮的酶法合成。

Enzymatic synthesis of 6'-deoxychalcone in cultured Glycyrrhiza echinata cells.

机构信息

Department of Applied Biological Science, College of Agriculture and Veterinary Medicine, Nihon University, Fujisaw, 252, Kanagawa, Japan.

出版信息

Plant Cell Rep. 1993 Jan;12(2):66-9. doi: 10.1007/BF00241936.

DOI:10.1007/BF00241936
PMID:24202070
Abstract

5-Deoxy-(iso)flavonoids are biosynthesized from 6'-deoxychalcone (isoliquiritigenin). The coaction of a reductase with chalcone synthase (CHS) has been established in soybean cells to be responsible for the synthesis of 6'-deoxychalcone. Western blot analysis of crude extracts from cultured cells of Glycyrrhiza echinata, another member of the Leguminosae, revealed proteins which cross-react with an antiserum raised against the soybean reductase. DEAE-Cellulose chromatography of the extract yielded fractions which showed CHS activity but not deoxychalcone synthase activity, and these fractions were also negative in Western blot analysis. In contrast, fractions displaying positive signals with the antiserum were also able to synthesize 6'-deoxychalcone/5-deoxyflavanone. These results indicate that in G. echinata, too, synthesis of 6'-deoxychalcone is likely to be performed by the coaction of the reductase and CHS. Induction of the reductase and CHS by yeast extract treatment of the cells was demonstrated.

摘要

5-脱氧(异)黄酮是由 6'-去氧查尔酮(异甘草素)生物合成的。已经在大豆细胞中证实,一种还原酶与查尔酮合酶(CHS)的共同作用负责 6'-去氧查尔酮的合成。甘草细胞培养细胞粗提物的 Western blot 分析显示,与大豆还原酶抗血清发生交叉反应的蛋白质。提取物的 DEAE-纤维素层析得到显示 CHS 活性但没有去氧查尔酮合酶活性的部分,并且这些部分在 Western blot 分析中也是阴性的。相比之下,与抗血清显示阳性信号的部分也能够合成 6'-去氧查尔酮/5-脱氧黄烷酮。这些结果表明,在甘草中,6'-去氧查尔酮的合成也可能是由还原酶和 CHS 的共同作用来完成的。已经证明酵母提取物处理细胞会诱导还原酶和 CHS 的表达。

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本文引用的文献

1
Stimulation of chalcone synthase activity by yeast extract in cultured Glycyrrhiza echinata cells and 5-deoxyflavanone formation by isolated protoplasts.酵母抽提物对甘草细胞培养中查尔酮合酶活性的刺激作用及分离原生质体中 5-脱氧黄酮的形成。
Plant Cell Rep. 1988 Jan;7(1):35-8. doi: 10.1007/BF00272973.
2
Flavonoids Released Naturally from Alfalfa Seeds Enhance Growth Rate of Rhizobium meliloti.紫花苜蓿种子自然释放的类黄酮可提高苜蓿根瘤菌的生长速率。
Plant Physiol. 1991 Mar;95(3):797-803. doi: 10.1104/pp.95.3.797.
3
Elicitor rapidly induces chalcone synthase mRNA in Phaseolus vulgaris cells at the onset of the phytoalexin defense response.
诱导子在菜豆细胞防御反应开始时迅速诱导查尔酮合酶 mRNA 的表达。
Proc Natl Acad Sci U S A. 1984 Sep;81(18):5724-8. doi: 10.1073/pnas.81.18.5724.
4
Organization and differential activation of a gene family encoding the plant defense enzyme chalcone synthase in Phaseolus vulgaris.菜豆中编码植物防御酶查尔酮合酶的基因家族的组织与差异激活
Mol Gen Genet. 1987 Dec;210(2):219-33. doi: 10.1007/BF00325687.
5
NAD(P)H-dependent 6'-deoxychalcone synthase activity in Glycyrrhiza echinata cells induced by yeast extract.酵母提取物诱导的光果甘草细胞中依赖NAD(P)H的6'-脱氧查尔酮合酶活性
Arch Biochem Biophys. 1988 Mar;261(2):458-62. doi: 10.1016/0003-9861(88)90362-1.
6
Defense strategies of soybean against the fungus Phytophthora megasperma f.sp. glycinea: a molecular analysis.大豆对真菌大豆疫霉大豆专化型的防御策略:分子分析
Trends Biochem Sci. 1988 Jan;13(1):23-7. doi: 10.1016/0968-0004(88)90014-x.
7
Phytoalexin synthesis in soybean cells: elicitor induction of reductase involved in biosynthesis of 6'-deoxychalcone.大豆细胞中的植保素合成:激发子诱导参与6'-脱氧查耳酮生物合成的还原酶
Arch Biochem Biophys. 1989 Jul;272(1):97-102. doi: 10.1016/0003-9861(89)90199-9.
8
Differential regulation of soybean chalcone synthase genes in plant defence, symbiosis and upon environmental stimuli.大豆查尔酮合酶基因在植物防御、共生及环境刺激下的差异调控
Mol Gen Genet. 1989 Aug;218(2):315-22. doi: 10.1007/BF00331284.
9
Induced plant responses to pathogen attack. Analysis and heterologous expression of the key enzyme in the biosynthesis of phytoalexins in soybean (Glycine max L. Merr. cv. Harosoy 63).植物对病原体攻击的诱导反应。大豆(Glycine max L. Merr. cv. Harosoy 63)植保素生物合成关键酶的分析及异源表达。
Eur J Biochem. 1991 Mar 14;196(2):423-30. doi: 10.1111/j.1432-1033.1991.tb15833.x.
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Isoliquiritigenin, a strong nod gene- and glyceollin resistance-inducing flavonoid from soybean root exudate.异甘草素,一种来自大豆根分泌物的具有强烈诱导结瘤基因和抗大豆抗毒素作用的类黄酮。
Appl Environ Microbiol. 1992 May;58(5):1705-10. doi: 10.1128/aem.58.5.1705-1710.1992.