Shiomi N
Department of Agricultural Chemistry, Faculty of Agriculture, Hokkaido University, Sapporo 060, Japan.
New Phytol. 1992 Nov;122(3):421-432. doi: 10.1111/j.1469-8137.1992.tb00069.x.
Contents of fructo-oligosaccharides and fructo-polysaccharides and activities of fructosyltransferases and invertase in asparagus roots harvested between July and November were studied by gel permeation chromatography (GPC) and high performance liquid chromatography (HPLC). Contents of total sugar and fructo-oligosaccharides and fructo-polysaccharides were very low in July, and then increased until September. During this period, sucrose accumulated first, second trisaccharides, and then tetra-, penta- and higher-saccharides increased in that order. 1-Kestose was the most predominant fructo-ohgosacchande isomer [degree of polymerization (DP) 3 ∼ 6]. The fructo-polysaccharide of DP ≥ 9 was 12.8 ∼ 21.7% of total sugar from September to November; polysaccharides estimated to be DP 20∼22 were just detectable. SST activities were very low in July, rose to a maximum in September and then decreased. Change in activity of SST was responsible for change in contents of sucrose and 1-kestose from July to November. 1 -fructosyltransferase (1 -FT) activities increased until September, were almost constant from October to November and then decreased slightly. 6 -fructosyltransferase (6 -FT) reached its highest activity early in October. 6 -SST (6-kestose producing enzyme) activity was very slight from July to November and was ∼ 1/1000 of SST activity in September. This activity does not contribute to the enzymatic synthesis of the saccharides of asparagus roots. Invertase activity was nearly constant throughout. The change of activities of SST, 1 -FT and 6 -FT paralleled closely the accumulation of sucrose, 1-kestose, neokestose and other saccharides. In vitro synthesis of fructo-oligosaccharides from sucrose at 0.4, 0.1 and 0.05 M, or from 1-kestose was investigated in a fraction prepared from asparagus roots harvested in September. 1-Kestose (isokestose, 3a), neokestose (3b), nystose (4a), 1 (l-β-D-fructofuranosyl) -6 (l-β-D-fructofuranosyl) -sucrose (4b: m= 0, n= 2; 4c: m= 1, n=1; 5a: m=3, n0; 5b: m=0, n=3; 5c: M=2, n=1; 5d: m=1, n=2) and a mixture of hexasaccharide-isomers were synthesized from 04 M sucrose in 60 h. In 0.05 and 0.1 M sucrose unidentified heptasaccharides were also produced. Octa- and higher-saccharide, as well as the saccharides synthesized from sucrose, were formed from 0.1 M 1-kestose. All of the saccharides synthesized from sucrose or 1-kestose by the asparagus enzyme preparation were identical to saccharides occurring naturally in the roots of asparagus.
采用凝胶渗透色谱法(GPC)和高效液相色谱法(HPLC)研究了7月至11月收获的芦笋根中低聚果糖和多聚果糖的含量以及果糖基转移酶和转化酶的活性。7月时总糖、低聚果糖和多聚果糖的含量非常低,随后持续增加直至9月。在此期间,蔗糖先积累,其次是三糖,然后四糖、五糖及更高聚糖依次增加。1-蔗果三糖是最主要的低聚果糖异构体[聚合度(DP)为3至6]。9月至11月,DP≥9的多聚果糖占总糖的12.8%至21.7%;估计DP为20至22的多糖仅可检测到。蔗糖合成酶(SST)活性在7月非常低,9月升至最高,然后下降。7月至11月蔗糖和1-蔗果三糖含量的变化是由SST活性的变化引起的。1-果糖基转移酶(1-FT)活性直至9月增加,10月至11月几乎恒定,然后略有下降。6-果糖基转移酶(6-FT)在10月初达到最高活性。6-SST(6-蔗果三糖产生酶)活性在7月至11月非常微弱,仅为9月SST活性的约1/1000。该活性对芦笋根中糖类的酶促合成没有贡献。转化酶活性在整个过程中几乎恒定。SST、1-FT和ó-FT活性的变化与蔗糖、1-蔗果三糖、新蔗果三糖和其他糖类的积累密切平行。在9月收获的芦笋根制备的组分中,研究了从0.4、0.1和0.05 M蔗糖或1-蔗果三糖体外合成低聚果糖的情况。在60小时内,从0.4 M蔗糖合成了1-蔗果三糖(异蔗果三糖,3a)、新蔗果三糖(3b)、蔗果四糖(4a)、1-(1-β-D-呋喃果糖基)-6-(1-β-D-呋喃果糖基)-蔗糖(4b: m = 0, n = 2;4c: m = 1, n = 1;5a: m = 3, n = 0;5b: m = 0, n = 3;5c: M = 2, n = 1;5d: m = 1, n = 2)和六糖异构体混合物。在0.05和0.1 M蔗糖中还产生了未鉴定的七糖。从0.1 M 1-蔗果三糖形成了八糖及更高聚糖,以及由蔗糖合成的糖类。芦笋酶制剂从蔗糖或1-蔗果三糖合成的所有糖类均与芦笋根中天然存在的糖类相同。