首页> 美国卫生研究院文献>Biochemical Journal >Differentiation-inducing factor from the slime mould Dictyostelium discoideum and its analogues. Synthesis structure and biological activity.
【2h】

Differentiation-inducing factor from the slime mould Dictyostelium discoideum and its analogues. Synthesis structure and biological activity.

机译:粘液菌盘基网柄菌及其类似物的分化诱导因子。合成结构和生物活性。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Previous work has led to the identification of a novel class of effector molecules [DIFs (differentiation-inducing factors) 1-3] released from the slime mould Dictyostelium discoideum. These substances induce stalk-cell differentiation in Dictyostelium discoideum and are thought to act as morphogens in the generation of the prestalk/prespore pattern during development. The DIFs are phenylalkan-1-ones, with chloro, hydroxy and methoxy substitution on the benzene ring. DIFs 1-3 and a number of their analogues have been synthesized by using a simple two-step procedure, and each analogue has been characterized by m.s., u.v. and n.m.r. spectroscopy. The crystal structure of synthetic DIF-1 [1-(3,5-dichloro-2,6-dihydroxy-4-methoxyphenyl)hexan-1-one, was investigated. The specific biological activity of each analogue was determined in a bioassay, where isolated Dictyostelium amoebae are induced to differentiate into stalk cells. The major biologically active substance, DIF-1, caused 50% stalk-cell differentiation at 1.8 x 10(-10) M; the C4 alkyl homologue (DIF-2) and C6 homologue possessed 40 and 16% of the activity of DIF-1 respectively. Further increase or decrease in the alkyl chain length resulted in a marked decrease in specific activity. The pattern of substitution on the benzene ring is a major determinant of bioactivity, since the specific activities of the 2,4-dihydroxy-6-methoxy and trihydroxy analogues were less than 1% of that of DIF-1. Substitution of bromine in DIF-1 had little effect on bioactivity; in contrast the activity of monochloro-DIF-1 (DIF-3) was diminished. There was no evidence for antagonism or synergy between DIF-1 and any of its analogues. This series of analogues will facilitate further studies in the biological effects and mode of action of DIF-1.
机译:以前的工作已导致鉴定出从粘液菌盘基网柄菌释放的一类新型效应分子[DIF(分化诱导因子)1-3]。这些物质在Disctyostelium Discoideum中诱导茎细胞分化,并被认为在发育过程中在前茎/芽孢形成过程中充当形态发生剂。 DIF是苯基烷烃-1-酮,在苯环上具有氯,羟基和甲氧基取代基。 DIF 1-3及其许多类似物是通过简单的两步程序合成的,每种类似物的特征是m.s.,u.v.。和n.m.r.光谱学。研究了合成的DIF-1 [1-(3,5-二氯-2,6-二羟基-4-甲氧基苯基)己-1-酮的晶体结构。在生物测定法中确定每种类似物的比生物学活性,在生物测定法中,分离出的变形杆菌属被诱导分化为茎细胞。主要的生物活性物质DIF-1在1.8 x 10(-10)M时引起50%的茎细胞分化。 C4烷基同系物(DIF-2)和C6同系物分别具有DIF-1活性的40%和16%。烷基链长度的进一步增加或减少导致比活性显着降低。苯环上的取代方式是生物活性的主要决定因素,因为2,4-二羟基-6-甲氧基和三羟基类似物的比活度不到DIF-1的1%。 DIF-1中的溴取代对生物活性影响不大。相反,一氯-DIF-1(DIF-3)的活性降低。没有证据表明DIF-1及其任何类似物之间存在拮抗作用或协同作用。该系列类似物将有助于进一步研究DIF-1的生物学效应和作用方式。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号