Matthysse A G, Thomas D L, White A R
Department of Biology, University of North Carolina, Chapel Hill 27599.
J Bacteriol. 1995 Feb;177(4):1076-81. doi: 10.1128/jb.177.4.1076-1081.1995.
Extracts of Agrobacterium tumefaciens incorporated UDP-[14C]glucose into cellulose. When the extracts were fractionated into membrane and soluble components, neither fraction was able to synthesize cellulose. A combination of the membrane and soluble fractions restored the activity found in the original extracts. Extracts of cellulose-minus mutants showed no significant incorporation of UDP-glucose into cellulose. When mixtures of the extracts were made, the mutants were found to fall into two groups: extracts of mutants from the first group could be combined with extracts of the second group to obtain cellulose synthesis. No synthesis was observed when extracts of mutants from the same group were mixed. The groups of mutants corresponded to the two operons identified in sequencing the cel genes (A. G. Matthysse, S. White, and R. Lightfoot. J. Bacteriol. 177:1069-1075, 1995). Extracts of mutants were fractionated into membrane and soluble components, and the fractions were mixed and assayed for the ability to synthesize cellulose. When the membrane fraction from mutants in the celDE operon was combined with the soluble fraction from mutants in the celABC operon, incorporation of UDP-glucose into cellulose was observed. In order to determine whether lipid-linked intermediates were involved in cellulose synthesis, permeablized cells were examined for the incorporation of UDP-[14C]glucose into material extractable with organic solvents. No radioactivity was found in the chloroform-methanol extract of mutants in the celDE operon, but radioactive material was recovered in the chloroform-methanol extract of mutants in the celABC operon. The saccharide component of these compounds was released after mild acid hydrolysis and was found to be mainly glucose for the celA insertion mutant and a mixture of cellobiose, cellotriose, and cellotetrose for the celB and celC insertion mutants. The radioactive compound extracted with chloroform-methanol form the celC insertion mutant was incorporated into cellulose by membrane preparations from celE mutants, which suggests that this compound is a lipid-linked intermediate in cellulose synthesis.
根癌土壤杆菌提取物能将UDP - [14C]葡萄糖掺入纤维素中。当将提取物分离为膜组分和可溶性组分时,这两种组分均无法合成纤维素。膜组分和可溶性组分的组合恢复了原始提取物中的活性。纤维素缺失突变体的提取物未显示UDP - 葡萄糖有显著掺入纤维素的情况。当制备提取物混合物时,发现突变体分为两组:第一组突变体的提取物可与第二组突变体的提取物组合以实现纤维素合成。同一组突变体的提取物混合时未观察到合成。这些突变体组与在对cel基因进行测序时鉴定出的两个操纵子相对应(A.G. 马西斯、S. 怀特和R. 莱特富特。《细菌学杂志》177:1069 - 1075, 1995)。将突变体的提取物分离为膜组分和可溶性组分,然后将这些组分混合并检测其合成纤维素的能力。当celDE操纵子中突变体的膜组分与celABC操纵子中突变体的可溶性组分组合时,观察到UDP - 葡萄糖掺入纤维素中。为了确定脂质连接的中间体是否参与纤维素合成,检查了透化细胞中UDP - [14C]葡萄糖掺入可被有机溶剂提取的物质中的情况。在celDE操纵子突变体的氯仿 - 甲醇提取物中未发现放射性,但在celABC操纵子突变体的氯仿 - 甲醇提取物中回收了放射性物质。这些化合物的糖类成分在温和酸水解后释放,发现celA插入突变体的主要是葡萄糖,而celB和celC插入突变体的是纤维二糖、纤维三糖和纤维四糖的混合物。从celC插入突变体中用氯仿 - 甲醇提取的放射性化合物被celE突变体的膜制剂掺入纤维素中,这表明该化合物是纤维素合成中的脂质连接中间体。