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本文引用的文献

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Biosynthesis of the salinosporamide A polyketide synthase substrate chloroethylmalonyl-coenzyme A from S-adenosyl-L-methionine.由S-腺苷-L-甲硫氨酸生物合成盐孢霉素A聚酮合酶底物氯乙基丙二酰辅酶A。
Proc Natl Acad Sci U S A. 2009 Jul 28;106(30):12295-300. doi: 10.1073/pnas.0901237106. Epub 2009 Jul 9.
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Genomic islands link secondary metabolism to functional adaptation in marine Actinobacteria.基因组岛将海洋放线菌的次生代谢与功能适应性联系起来。
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Carboxylation mechanism and stereochemistry of crotonyl-CoA carboxylase/reductase, a carboxylating enoyl-thioester reductase.巴豆酰辅酶A羧化酶/还原酶(一种羧化烯酰硫酯还原酶)的羧化机制及立体化学
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Biosynthesis of polyketide synthase extender units.聚酮合酶延伸单元的生物合成。
Nat Prod Rep. 2009 Jan;26(1):90-114. doi: 10.1039/b801658p.
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Dentigerumycin: a bacterial mediator of an ant-fungus symbiosis.齿霉素:一种蚂蚁与真菌共生关系的细菌介导物。
Nat Chem Biol. 2009 Jun;5(6):391-3. doi: 10.1038/nchembio.159. Epub 2009 Mar 29.
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Engineered biosynthesis of antiprotealide and other unnatural salinosporamide proteasome inhibitors.抗蛋白酶抑制肽及其他非天然盐孢菌素蛋白酶体抑制剂的工程化生物合成。
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7
Mutasynthesis of fluorosalinosporamide, a potent and reversible inhibitor of the proteasome.氟沙林孢酰胺的突变生物合成,一种有效的蛋白酶体可逆抑制剂。
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Discovery and characterization of a marine bacterial SAM-dependent chlorinase.一种海洋细菌依赖S-腺苷甲硫氨酸的二氢卟吩酶的发现与特性研究
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Genome sequencing reveals complex secondary metabolome in the marine actinomycete Salinispora tropica.基因组测序揭示了热带盐孢菌这一海洋放线菌中的复杂次生代谢组。
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10
Synthesis of C5-dicarboxylic acids from C2-units involving crotonyl-CoA carboxylase/reductase: the ethylmalonyl-CoA pathway.通过巴豆酰辅酶A羧化酶/还原酶由C2单位合成C5-二羧酸:乙基丙二酰辅酶A途径。
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源自α,β-不饱和脂肪酸的盐孢菌素的生物合成:对扩展聚酮合酶多样性的意义

Biosynthesis of salinosporamides from alpha,beta-unsaturated fatty acids: implications for extending polyketide synthase diversity.

作者信息

Liu Yuan, Hazzard Christopher, Eustáquio Alessandra S, Reynolds Kevin A, Moore Bradley S

机构信息

Scripps Institution of Oceanography, University of California at San Diego, La Jolla, California 92093-0204, USA.

出版信息

J Am Chem Soc. 2009 Aug 5;131(30):10376-7. doi: 10.1021/ja9042824.

DOI:10.1021/ja9042824
PMID:19601645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2737082/
Abstract

A new series of coenzyme A-tethered polyketide synthase extender units were discovered in relation to the biosynthesis of the salinosporamide family of anticancer agents from the marine bacterium Salinispora tropica. In vivo and in vitro experiments revealed that the crotonyl-CoA reductase/carboxylase SalG has broad substrate tolerance toward 2-alkenyl-CoAs that give rise to the salinosporamide C-2 substitution pattern.

摘要

在与来自热带盐孢菌的抗癌剂盐孢酰胺家族生物合成相关的研究中,发现了一系列新的辅酶A连接的聚酮合酶延伸单元。体内和体外实验表明,巴豆酰辅酶A还原酶/羧化酶SalG对导致盐孢酰胺C-2取代模式的2-烯基辅酶A具有广泛的底物耐受性。