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生长培养基中葡萄糖和酵母提取物水平对博戈里假丝酵母中羟基二十二烷酸槐糖苷产量的调控

Regulation of hydroxydocosanoic acid sophoroside production in Candida bogoriensis by the levels of glucose and yeast extract in the growth medium.

作者信息

Cutler A J, Light R J

出版信息

J Biol Chem. 1979 Mar 25;254(6):1944-50.

PMID:422563
Abstract

Cells of Candida bogoriensis produce as a major extracellular lipid 13-[(2'-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]docosanoic acid 6',6''-diacetate (Ac2Glc2HDA), the diacetylated sophoroside of 13-hydroxydocosanoic acid (HDA), along with mono- and unacetylated derivatives. The HDA glycolipid production is greater than 2 g/liter when cells are grown on a "standard" medium of 3% glucose and 0.15% yeast extract. Either lowering the glucose concentration (0.5 to 2.0% glucose, at 0.2% yeast extract) or raising the yeast extract concentration (2 to 4% yeast extract at 3% glucose) greatly decreased the yield of this glycolipid, as well as its rate of synthesis measured by [14C]acetate incorporation. Total HDA production was also depressed on the low glucose medium, as was the activity of UDP-glucose:HDA glucosyltransferase, the first enzyme involved in the synthesis of Ac2Glc2HDA from HDA. Levels of acetyl-CoA:Glc2HDA acetyltransferase were not decreased by growth on a low glucose medium, however, even under conditions in which glycolipid production was less than 4% of that found in the standard medium. Low levels of the HDA glycolipids were monitored by high pressure liquid chromatography of their p-bromophenacyl esters, formed by the action of alpha,beta-dibromoacetophenone on the sodium salt of the lipid in the presence of a crown reagent catalyst. This regulation of extracellular Ac2Glc2HDA production by the nutrient composition of the growth medium may represent an important property in the adaptation of C. bogoriensis to its natural environment, the phyllosphere.

摘要

博戈里假丝酵母细胞产生的主要细胞外脂质为13-[(2'-O-β-D-吡喃葡萄糖基-β-D-吡喃葡萄糖基)氧基]二十二烷酸6',6''-二乙酸酯(Ac2Glc2HDA),即13-羟基二十二烷酸(HDA)的二乙酰化槐糖脂,同时还产生单乙酰化和未乙酰化的衍生物。当细胞在含有3%葡萄糖和0.15%酵母提取物的“标准”培养基上生长时,HDA糖脂的产量大于2克/升。降低葡萄糖浓度(0.5%至2.0%葡萄糖,酵母提取物浓度为0.2%)或提高酵母提取物浓度(3%葡萄糖时酵母提取物浓度为2%至4%)都会大幅降低这种糖脂的产量及其通过[14C]乙酸掺入法测得的合成速率。在低葡萄糖培养基上,HDA的总产量也会降低,参与从HDA合成Ac2Glc2HDA的第一种酶UDP-葡萄糖:HDA葡糖基转移酶的活性也是如此。然而,即使在糖脂产量低于标准培养基中糖脂产量4%的条件下,生长在低葡萄糖培养基上时乙酰辅酶A:Glc2HDA乙酰转移酶的水平也不会降低。通过高压液相色谱法检测其对溴苯甲酰酯(由α,β-二溴苯乙酮在冠醚试剂催化剂存在下作用于脂质钠盐形成)来监测低水平的HDA糖脂。生长培养基的营养成分对细胞外Ac2Glc2HDA产生的这种调节可能代表了博戈里假丝酵母适应其自然环境——叶际的一项重要特性。

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