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耐冷米根霉在非无菌开放发酵条件下生产壳聚糖

Chitosan production by psychrotolerant Rhizopus oryzae in non-sterile open fermentation conditions.

作者信息

Tasar Ozden Canli, Erdal Serkan, Taskin Mesut

机构信息

Central Research Laboratory Application and Research Centre, Adiyaman University, Adiyaman, Turkey.

Department of Biology, Science Faculty, Ataturk University, Erzurum, Turkey.

出版信息

Int J Biol Macromol. 2016 Aug;89:428-33. doi: 10.1016/j.ijbiomac.2016.05.007. Epub 2016 May 3.

Abstract

A new chitosan producing fungus was locally isolated from soil samples collected around Erzurum, Turkey and identified as Rhizopus oryzae PAS 17 (GenBank accession number KU318422.1). Cultivation in low cost non-sterile conditions was achieved by exploiting its ability to grow at low temperature and pH, thus, undesired microbial contamination could be eliminated when appropriate culture conditions (incubation temperature as 15°C and initial pH of the medium as 4.5) were selected. Medium composition and culture conditions were optimized using Taguchi orthogonal array (OA) design of experiment (DOE). An OA layout of L16 (4(5)) was constructed with five most influensive factors at four levels on chitosan production like, carbon source (molasses), metal ion (Mg(2+)), inoculum amount, agitation speed and incubation time. The optimal combinations of factors (molasses, 70ml/l; MgSO4·7H2O, 0.5g/l; inoculum, 6.7×10(6) spores/disc; agitation speed, 150rpm and incubation time, 8days) obtained from the proposed DOE methodology was further validated by analysis of variance (ANOVA) test and the results revealed the increment of chitosan and biomass yields of 14.45 and 8.58 folds from its unoptimized condition, respectively.

摘要

从土耳其埃尔祖鲁姆周边采集的土壤样本中,本地分离出一种新的壳聚糖生产真菌,并鉴定为米根霉PAS 17(GenBank登录号KU318422.1)。利用其在低温和低pH值下生长的能力,实现了在低成本非无菌条件下的培养,因此,当选择合适的培养条件(培养温度为15°C,培养基初始pH值为4.5)时,可以消除不期望的微生物污染。使用田口正交阵列(OA)实验设计(DOE)对培养基组成和培养条件进行了优化。构建了L16(4(5))的OA布局,其中包括对壳聚糖生产有四个水平影响最大的五个因素,即碳源(糖蜜)、金属离子(Mg(2+))、接种量、搅拌速度和培养时间。通过方差分析(ANOVA)测试进一步验证了从所提出的DOE方法中获得的因素最佳组合(糖蜜,70ml/l;MgSO4·7H2O,0.5g/l;接种物,6.7×10(6)个孢子/盘;搅拌速度,150rpm;培养时间,8天),结果显示壳聚糖和生物量产量分别比未优化条件下增加了14.45倍和8.58倍。

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