α-Amylase activity during pullulan production and α-amylase gene analyses of Aureobasidium pullulans

被引:20
|
作者
Manitchotpisit, Pennapa [1 ,2 ]
Skory, Christopher D. [3 ]
Leathers, Timothy D. [3 ]
Lotrakul, Pongtharin [1 ]
Eveleigh, Douglas E. [4 ]
Prasongsuk, Sehanat [1 ]
Punnapayak, Hunsa [1 ]
机构
[1] Chulalongkorn Univ, Plant Biomass Utilizat Res Unit, Dept Bot, Fac Sci, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Biol Sci Program, Fac Sci, Bangkok 10330, Thailand
[3] ARS, Renewable Product Technol Res Unit, Natl Ctr Agr Utilizat Res, USDA, Peoria, IL 61604 USA
[4] Rutgers State Univ, Dept Biochem & Microbiol, Sch Environm & Biol Sci, Newark, NJ 08901 USA
关键词
Aureobasidium pullulans; alpha-Amylase; Molecular weight; Pullulan; MOLECULAR-WEIGHT PULLULAN; STRAINS; POLYSACCHARIDE; ADHESION;
D O I
10.1007/s10295-010-0899-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aureobasidium pullulans is the source of commercially produced pullulan, a high molecular weight polysaccharide that is used in the manufacture of edible films. It has been proposed that alpha-amylase decreases the molecular weight of pullulan in late cultures. Based on a recent phylogenetic analysis, five representative strains were chosen to study the relationship between alpha-amylase and pullulan production. In sucrose-grown cultures, pullulan yields increased over time while the molecular weight of pullulan generally decreased. However, no alpha-amylase activity was detected in these cultures. Low levels of alpha-amylase were present in starch-grown culture, but pullulan analysis was complicated by residual starch. To facilitate further studies on the role of alpha-amylase in the reduction of pullulan molecular weight, the alpha-amylase gene from A. pullulans NRRL Y-12974 was cloned and characterized. The coding region of the complete alpha-amylase gene contains 2,247 bp, including 7 introns and 8 exons. The putative mRNA was 1,878 bp long, encoding an alpha-amylase of 625 amino acid residues. Southern blot analysis indicated that there was only one copy of this gene in the genome. Reverse transcription-polymerase chain reaction (RT-PCR) analysis indicated that the gene was transcribed in both sucrose- and starch-grown cultures. It is possible that very low levels of alpha-amylase attack the minor maltotetraose subunits of pullulan and cause the reduction of molecular weight.
引用
收藏
页码:1211 / 1218
页数:8
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