Fatty acid desaturation in methylotrophic yeast Hansenula polymorpha strain CBS 1976 and unsaturated fatty acid auxotrophic mutants

Sarintip Anamnart , Ilya Tolstorukov , Yoshinobu Kaneko , Satoshi Harashima
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引用次数: 20

Abstract

Analysis of fatty acid composition in wild-type cells of Hansenula polymorpha strain CBS 1976 revealed the presence of 18 : 1 (Δ9), 18 : 2 (Δ9,12) and 18 : 3 (Δ9,12,15) unsaturated fatty acids (UFAs), indicating that the α-linolenic desaturation pathway operates in this yeast. H. polymorpha cells also showed ability for uptake and incorporation of exogenous UFAs. By ethyl methanesulfonate mutagenesis, nine unsaturated fatty acid auxotrophic mutants of H. polymorpha were isolated. These mutants exhibited the growth arrest phenotype on nutrient medium and on nutrient medium supplemented with saturated fatty acids, but grew on media supplemented with various UFAs. Genetic analysis revealed that single recessive nuclear mutation conferred Ufa auxotrophy on these mutants. Fatty acid analysis by gas chromatography showed the accumulation of 18 : 0 but a decrease in the amount of 18 : 1 and 18 : 2 in mutant cells compared with the wild-type cells. Integrated physiological and genetical data suggested that mutations in all mutants occurred in one gene and probably led to defects in Δ9-desaturation pathway.

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甲基营养酵母菌CBS 1976与不饱和脂肪酸营养缺陷突变体的脂肪酸去饱和
对野生型多态Hansenula polymorpha菌株CBS 1976细胞的脂肪酸组成进行分析,发现存在18:1 (Δ9)、18:2 (Δ9,12)和18:3 (Δ9,12,15)不饱和脂肪酸(UFAs),表明该酵母具有α-亚麻酸去饱和途径。H. polymorpha细胞也表现出摄取和结合外源性UFAs的能力。采用甲磺酸乙酯诱变方法,分离得到9个多形血蓼不饱和脂肪酸营养缺陷突变体。这些突变体在营养培养基和添加饱和脂肪酸的营养培养基上表现为生长停滞表型,但在添加各种不饱和脂肪酸的营养培养基上生长。遗传分析表明,单隐性核突变使这些突变体产生Ufa营养不良。气相色谱法分析表明,突变体细胞中脂肪酸的积累量为18:0,而18:1和18:2的含量较野生型细胞有所减少。综合生理和遗传数据表明,所有突变体的突变发生在一个基因上,可能导致Δ9-desaturation通路的缺陷。
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