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首页> 外文期刊>Applied Microbiology and Biotechnology >Isolation and characterization of an efficient bacterial cellulose producer strain in agitated culture: Gluconacetobacter hansenii P2A
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Isolation and characterization of an efficient bacterial cellulose producer strain in agitated culture: Gluconacetobacter hansenii P2A

机译:搅拌培养中高效细菌纤维素生产菌的分离和鉴定:汉逊氏糖杆菌P2A

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In this study, typical niches of acetic acid bacteria were screened for isolation of cellulose producer strains. Hestrin Schramm broth was used as enrichment and production media. Only nine out of 329 isolates formed thick biofilms on liquid surface and were identified as potential cellulose producers. Physiological and biochemical tests proved that all cellulose producers belonged to Gluconacetobacter genus.Most productive and mutation-resistant strain was subjected to 16S rRNA sequence analysis and identified as Gluconacetobacter hansenii P2A due to 99.8 % sequence similarity. X-ray diffraction analysis proved that the biofilm conformed to Cellulose I crystal structure, rich in Iα mass fraction. Static cultivation of G. hansenii P2A in HS medium resulted with 1.89±0.08 g/l of bacterial cellulose production corresponding to 12.0±0.3 % yield in terms of substrate consumption. Shaking and agitation at 120 rpm aided in enhancement of the amount and yield of produced cellulose. Productivity and yield reached up to 3.25± 0.11 g/l and 17.20±0.14 % in agitated culture while a slight decrease from 78.7 % to 77.3 % was observed in the crystallinity index.
机译:在这项研究中,筛选出典型的乙酸菌ni以分离纤维素生产菌株。 Hestrin Schramm肉汤用作浓缩和生产培养基。在329个分离物中,只有9个在液体表面形成了厚厚的生物膜,并被确定为潜在的纤维素生产者。生理生化试验证明,所有纤维素生产者均属于葡糖杆菌属。对大多数具有生产性和抗突变性的菌株进行16S rRNA序列分析,由于其99.8%的序列相似性,被鉴定为汉森氏杆菌P2A。 X射线衍射分析证明该生物膜符合纤维素I晶体结构,富含Iα质量分数。在HS培养基中静态培养汉逊G. P2A,产生1.89±0.08 g / l的细菌纤维素产量,相当于底物消耗的12.0±0.3%产量。以120 rpm的速度摇动和搅拌有助于提高纤维素的产量和产量。在搅拌培养中,生产率和产率分别达到3.25±0.11g / l和17.20±0.14%,而结晶度指数从78.7%略微下降至77.3%。

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