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费氏青霉中利用细胞外复合多糖中的磷酸胆碱作为细胞质胆碱衍生物的来源

Utilization of phosphocholine from extracellular complex polysaccharide as a source of cytoplasmic choline derivatives in Penicillium fellutanum.

作者信息

Park Y I, Buszko M L, Gander J E

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville 32611-0700, USA.

出版信息

J Bacteriol. 1997 Feb;179(4):1186-92. doi: 10.1128/jb.179.4.1186-1192.1997.

Abstract

Penicillium fellutanum produces a phosphorylated, choline-containing extracellular polysaccharide, peptidophosphogalactomannan (pP(x)GM) [where x is the number of phosphodiester residues]). The 13C-methyl-labeled pP(x)GM ([methyl-13C]pP(x)GM) was prepared from the cultures supplemented with L-[methyl-13C]methionine and was used as a probe to monitor the fate of phosphocholine in this polymer. The addition of [methyl-13C]pP(x)GM to growing cultures in low-phosphate medium resulted in the disappearance within 5 days of [methyl-13C]phosphocholine and N,N'-dimethylphosphoethanolamine from the added [methyl-13C]pP(x)GM. Two 13C-methyl-enriched cytoplasmic solutes, choline-O-sulfate and glycine betaine, were found in mycelial extracts, suggesting that phosphocholine-containing extracellular pP(x)GM of P. fellutanum is a precursor of intracellular choline-O-sulfate and glycine betaine. The mycelia cultured in low-phosphate (2 mM) medium contained glycine betaine and 1.5-fold more choline-O-sulfate than those grown in high-phosphate (20 mM) medium. The high levels of extracellular nonspecific phosphocholine:phosphocholine hydrolase and acid phosphomonoesterase observed in the low-phosphate culture medium are likely related to the release of phosphocholine from pP(x)GM and hydrolysis of phosphocholine, respectively. These results suggest that extracellular pP(x)GM of P. fellutanum provides phosphate needed as the environment becomes depleted of this nutrient. Choline, in excess of that needed immediately, is stored in the cytoplasm in forms that can be reutilized.

摘要

费氏青霉产生一种含磷酸化胆碱的细胞外多糖,即肽磷酸半乳甘露聚糖(pP(x)GM)[其中x为磷酸二酯残基的数量]。13C-甲基标记的pP(x)GM([甲基-13C]pP(x)GM)由添加L-[甲基-13C]甲硫氨酸的培养物制备而成,并用作监测该聚合物中磷酸胆碱去向的探针。在低磷培养基中向生长的培养物中添加[甲基-13C]pP(x)GM,导致添加的[甲基-13C]pP(x)GM中的[甲基-13C]磷酸胆碱和N,N'-二甲基磷酸乙醇胺在5天内消失。在菌丝体提取物中发现了两种富含13C-甲基的细胞质溶质,即胆碱-O-硫酸盐和甘氨酸甜菜碱,这表明费氏青霉含磷酸胆碱的细胞外pP(x)GM是细胞内胆碱-O-硫酸盐和甘氨酸甜菜碱的前体。在低磷(2 mM)培养基中培养的菌丝体含有甘氨酸甜菜碱,且胆碱-O-硫酸盐的含量比在高磷(20 mM)培养基中生长的菌丝体多1.5倍。在低磷培养基中观察到的高水平细胞外非特异性磷酸胆碱:磷酸胆碱水解酶和酸性磷酸单酯酶可能分别与pP(x)GM中磷酸胆碱的释放和磷酸胆碱的水解有关。这些结果表明,随着环境中这种营养物质的耗尽,费氏青霉的细胞外pP(x)GM提供了所需的磷酸盐。过量的胆碱会以可再利用的形式储存在细胞质中。

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