首页> 外文期刊>Plant physiology >EXPRESSION OF THE HEVEA BRASILIENSIS (HBK) MULL ARG 3-HYDROXY-3-METHYLGLUTARYL-COENZYME A REDUCTASE 1 IN TOBACCO RESULTS IN STEROL OVERPRODUCTION
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EXPRESSION OF THE HEVEA BRASILIENSIS (HBK) MULL ARG 3-HYDROXY-3-METHYLGLUTARYL-COENZYME A REDUCTASE 1 IN TOBACCO RESULTS IN STEROL OVERPRODUCTION

机译:固醇过量生产的烟草结果中巴西啤酒花乙型肝炎(HBK)3-羟基-3-甲基谷氨酸-辅酶A还原酶1的表达

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摘要

A genomic fragment encoding one (HMGR1) of the three 3-hydroxy-3-methylglutaryl coenzyme A reductases (HMGRs) from Hevea brasiliensis (H.B.K.) Mull. Arg. (M.-L. Chye, C.-T. Tan, N.-H. Chua [1992] Plant Mol Biol 19: 473-484) was introduced into Nicotiana tabacum L. cv xanthi via Agrobacterium transformation to study the influence of the hmg? gene product on plant isoprenoid biosynthesis. Transgenic plants were morphologically indistinguishable from control wild-type plants and displayed the same developmental pattern. Transgenic lines showed an increase in the level of total sterols up to 6-fold, probably because of an increased expression level of hmg1 mRNA and a corresponding increased enzymatic activity for HMGR, when compared with the level of total sterols from control lines not expressing the hmg1 transgene. In addition to the pathway end products, campesterol, sitosterol, and stigmasterol, some biosynthetic intermediates such as cycloartenol also accumulated in transgenic tissues. Most of the overproduced sterols were detected as steryl-esters and were likely to be stored in cytoplasmic lipid bodies. These data strongly support the conclusion that plant HMGR is a key limiting enzyme in phytosterol biosynthesis. [References: 39]
机译:一种基因组片段,编码来自巴西橡胶树(H.B.K.)Mull的三个3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR)中的一个(HMGR1)。精氨酸(M.-L.Chye,C.-T.Tan,N.-H.Chua [1992] Plant Mol Biol 19:473-484)通过农杆菌转化被引入到烟草L.cv Xanthi中以研究烟草的影响。嗯?基因产物对植物类异戊二烯生物合成的影响。转基因植物在形态上与对照野生型植物没有区别,并显示出相同的发育模式。转基因品系显示总固醇水平提高了6倍,这可能是因为与未表达对照的对照品系的总固醇水平相比,hmg1 mRNA的表达水平增加了,HMGR的酶活性也相应增加了。 hmg1转基因。除了途径终产物,菜油甾醇,谷固醇和豆甾醇,一些生物合成中间体,例如环戊烯醇也积累在转基因组织中。大多数过量生产的固醇被检测为固醇酯,并可能存储在细胞质脂质体中。这些数据有力地支持了植物HMGR是植物甾醇生物合成中的关键限制性酶的结论。 [参考:39]

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