Al-Qsous Suha, Carpentier Emilie, Klein-Eude Dominique, Burel Carole, Mareck Alain, Dauchel Hélène, Gomord Véronique, Balangé Alain Pierre
Laboratoire Signaux et régulation chez les végétaux, CNRS UMR 6037, IFRMP 23, Université de Rouen, 76821 Mont-Saint-Aignan Cedex, France.
Planta. 2004 Jun;219(2):369-78. doi: 10.1007/s00425-004-1246-1. Epub 2004 Mar 27.
Pectin methylesterases (PMEs) are ubiquitous enzymes present in the plant cell wall. They catalyse the demethylesterification of homogalacturonic acid units of pectins, which, in turn, can be associated with different physiological phenomena. In this study, different flax (Linum usitatissimum L.) PME isoforms were observed: neutral (pI 7.0 and 7.5, MW: 110 kDa), basic (pI 8.3 and 8.5, MW: 110 kDa) and very basic (pI>9.5, MW: 38 kDa). In an attempt to identify most of the expressed cell wall LuPME isoforms, polyclonal antibodies were raised against a conserved region of PME. These antibodies allowed the purification of the very basic PME isoform (pI 9.5, MW: 36 kDa) from flax cells, designated LuPME5. This isoform corresponds to the Lupme5 cDNA isolated, at the same time, from flax hypocotyls, by using the RACE-PCR technique. Semi-quantitative PCR experiments showed that the Lupme5 transcript was highly expressed in the hypocotyl zones where elongation is being achieved. Thus, this enzyme may be involved in cell wall stiffening.
果胶甲酯酶(PMEs)是植物细胞壁中普遍存在的酶。它们催化果胶中同型半乳糖醛酸单元的去甲基酯化反应,这反过来又可能与不同的生理现象相关。在本研究中,观察到了不同的亚麻(Linum usitatissimum L.)PME同工型:中性(pI 7.0和7.5,分子量:110 kDa)、碱性(pI 8.3和8.5,分子量:110 kDa)和极碱性(pI>9.5,分子量:38 kDa)。为了鉴定大多数表达的细胞壁LuPME同工型,针对PME的保守区域制备了多克隆抗体。这些抗体能够从亚麻细胞中纯化出极碱性PME同工型(pI 9.5,分子量:36 kDa),命名为LuPME5。该同工型与同时通过RACE-PCR技术从亚麻下胚轴中分离出的Lupme5 cDNA相对应。半定量PCR实验表明,Lupme5转录本在正在进行伸长的下胚轴区域中高度表达。因此,这种酶可能参与细胞壁的硬化过程。