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An epigenetic modifier induces production of (10′S)-verruculide B an inhibitor of protein tyrosine phosphatases by Phoma sp. nov. LG0217 a fungal endophyte of Parkinsonia microphylla

机译:表观遗传修饰剂诱导(10S)-verruculide B的产生Phoma sp。是蛋白质酪氨酸磷酸酶的抑制剂。十一月LG0217小叶帕金森菌的真菌内生菌

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摘要

Incorporation of the histone deacetylase (HDAC) inhibitor, suberoylanilide hydroxamic acid (SAHA), to a culture broth of the endophytic fungus Phoma sp. nov. LG0217 isolated from Parkinsonia microphylla changed its metabolite profile and resulted in the production of (10′S)-verruculide B (>1), vermistatin (>2) and dihydrovermistatin (>3). When cultured in the absence of the epigenetic modifier, it produced a new metabolite, (S,Z)-5-(3′,4′-dihydroxybutyldiene)-3-propylfuran-2(5H)-one (>4) together with nafuredin (>5). The structure of >4 was elucidated by spectroscopic analyses and its absolute configuration was determined by application of the modified Mosher’s ester method. The absolute structure of (10′S)-verruculide B was determined as 5-[(10′S,2′E,6′E)-10′,11′-dihydroxy-3′,7′,11′-trimethyldodeca-2′,6′-dien-1′-yl]-(3R)-6,8-dihydroxy-3-methylisochroman-1-one (>1) with the help of CD and NOE data. Compound >1 inhibited the activity of protein tyrosine phosphatases (PTPs) 1B (PTP1B), Src homology 2-containing PTP 1 (SHP1) and T-cell PTP (TCPTP) with IC50 values of 13.7±3.4, 8.8±0.6, and 16.6±3.8 μM, respectively. Significance of these activities and observed modest selectivity of >1 for SHP1 over PTP1B and TCPTP is discussed.
机译:将组蛋白脱乙酰基酶(HDAC)抑制剂次戊酰苯胺异羟肟酸(SAHA)掺入到内生真菌Phoma sp。的培养液中。十一月分离自小叶帕金森氏菌的LG0217改变了其代谢产物谱并导致产生(10'S)-verruculide B(> 1 ),Vermistatin(> 2 )和dihydroovermistatin( > 3 )。在没有表观遗传修饰剂的情况下培养时,它会产生新的代谢产物,(S,Z)-5-(3',4'-二羟基丁基二烯)-3-丙基呋喃-2(5H)-one(> 4 < / strong>)和那呋丁(> 5 )。通过光谱分析阐明了> 4 的结构,并通过应用改进的Mosher酯法确定了其绝对构型。 (10'S)-小杀虫剂B的绝对结构确定为5-[(10'S,2'E,6'E)-10',11'-二羟基-3',7',11'-三甲基十二烷基-2',6'-dien-1'-yl]-(3R)-6,8-dihydroxy-3-methylisochroman-1-one(> 1 )借助CD和NOE数据。化合物> 1 抑制蛋白酪氨酸磷酸酶(PTP)1B(PTP1B),含Src同源性2的PTP 1(SHP1)和T细胞PTP(TCPTP)的活性,IC50值为13.7±3.4,分别为8.8±0.6和16.6±3.8μM。讨论了这些活性的意义以及观察到的SHP1对PTP1B和TCPTP的适度选择性> 1

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