Shevchik V E, Condemine G, Robert-Baudouy J, Hugouvieux-Cotte-Pattat N
Laboratoire de Génétique Moléculaire des Microorganismes et des Interactions Cellulaires, UMR-CNRS 5577, INSA, F-69621 Villeurbanne Cedex, France.
J Bacteriol. 1999 Jul;181(13):3912-9. doi: 10.1128/JB.181.13.3912-3919.1999.
Erwinia chrysanthemi 3937 secretes into the external medium several pectinolytic enzymes, among which are eight isoenzymes of the endo-cleaving pectate lyases: PelA, PelB, PelC, PelD, and PelE (family 1); PelI (family 4); PelL (family 3); and PelZ (family 5). In addition, one exo-cleaving pectate lyase, PelX (family 3), has been found in the periplasm of E. chrysanthemi. The E. chrysanthemi 3937 gene kdgC has been shown to exhibit a high degree of similarity to the genes pelY of Yersinia pseudotuberculosis and pelB of Erwinia carotovora, which encode family 2 pectate lyases. However, no pectinolytic activity has been assigned to the KdgC protein. After verification of the corresponding nucleotide sequence, we cloned a longer DNA fragment and showed that this gene encodes a 553-amino-acid protein exhibiting an exo-cleaving pectate lyase activity. Thus, the kdgC gene was renamed pelW. PelW catalyzes the formation of unsaturated digalacturonates from polygalacturonate or short oligogalacturonates. PelW is located in the bacterial cytoplasm. In this compartment, PelW action could complete the degradation of pectic oligomers that was initiated by the extracellular or periplasmic pectinases and precede the action of the cytoplasmic oligogalacturonate lyase, Ogl. Both cytoplasmic pectinases, PelW and Ogl, seem to act in sequence during oligogalacturonate depolymerization, since oligomers longer than dimers are very poor substrates for Ogl but are good substrates for PelW. The estimated number of binding subsites for PelW is three, extending from subsite -2 to +1, while it is probably two for Ogl, extending from subsite -1 to +1. The activities of the two cytoplasmic lyases, PelW and Ogl, are dependent on the presence of divalent cations, since both enzymes are inhibited by EDTA. In contrast to the extracellular pectate lyases, Ca2+ is unable to restore the activity of PelW or Ogl, while several other cations, including Co2+, Mn2+, and Ni2+, can activate both cytoplasmic lyases.
菊欧文氏菌3937分泌多种果胶分解酶到细胞外培养基中,其中包括8种内切果胶酸裂解酶同工酶:PelA、PelB、PelC、PelD和PelE(家族1);PelI(家族4);PelL(家族3);以及PelZ(家族5)。此外,在菊欧文氏菌的周质中发现了一种外切果胶酸裂解酶PelX(家族3)。已证明菊欧文氏菌3937基因kdgC与假结核耶尔森氏菌的pelY基因和胡萝卜软腐欧文氏菌的pelB基因具有高度相似性,这两个基因编码家族2果胶酸裂解酶。然而,尚未赋予KdgC蛋白果胶分解活性。在验证了相应的核苷酸序列后,我们克隆了一个更长的DNA片段,并表明该基因编码一种具有外切果胶酸裂解酶活性的553个氨基酸的蛋白质。因此,kdgC基因被重新命名为pelW。PelW催化从聚半乳糖醛酸或短寡聚半乳糖醛酸形成不饱和二半乳糖醛酸。PelW位于细菌细胞质中。在这个区室中,PelW的作用可以完成由细胞外或周质果胶酶启动的果胶寡聚物的降解,并在细胞质寡聚半乳糖醛酸裂解酶Ogl作用之前发生。两种细胞质果胶酶PelW和Ogl在寡聚半乳糖醛酸解聚过程中似乎是按顺序起作用的,因为比二聚体更长的寡聚物是Ogl的非常差的底物,但却是PelW的良好底物。PelW的结合亚位点估计数量为3个,从亚位点-2延伸到+1,而Ogl可能为2个,从亚位点-1延伸到+1。两种细胞质裂解酶PelW和Ogl的活性依赖于二价阳离子的存在,因为这两种酶都被EDTA抑制。与细胞外果胶酸裂解酶不同,Ca2+无法恢复PelW或Ogl的活性,而包括Co2+、Mn2+和Ni2+在内的其他几种阳离子可以激活这两种细胞质裂解酶。