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锰(II)对地衣芽孢杆菌ATCC 9945A生理特性及γ-聚谷氨酸形成的影响。

Effects of manganese (II) on Bacillus licheniformis ATCC 9945A physiology and gamma-poly(glutamic acid) formation.

作者信息

Cromwick A M, Gross R A

机构信息

University of Massachusetts Lowell, Department of Chemistry 01854, USA.

出版信息

Int J Biol Macromol. 1995 Oct;17(5):259-67. doi: 10.1016/0141-8130(95)98153-p.

Abstract

Bacillus licheniformis ATCC 9945A was cultivated in shake flasks using citrate (12 gl-1), glutamate (20 gl-1) and glycerol (80 gl-1) as carbon sources for cell growth and gamma-poly(glutamic acid) (gamma-PGA) production. The effect of the MnSO4 concentration in the medium over a range from 0.0 to 615 microns was studied. The number of viable cells increased for all concentrations of MnSO4 from approximately 10(5) to 10(9) colony-forming units (cfu) ml-1 by the early stationary phase (24 h). However, after 50 h, the cell viability decreased rapidly for relatively lower MnSO4 concentrations (0.615 and 0 microns). The utilization of carbon sources by B. licheniformis was greater for cultures containing 33.8 and 615 microns MnSO4 relative to cultures with no added MnSO4. For example, cultures with 615 microns MnSO4 utilized 37, 54 and 93% and cultures with no added MnSO4 utilized 19, 10 and 17% of glutamate, glycerol and citrate, respectively. The gamma-PGA volumetric yield increased from approximately 5 to 17 gl-1 for corresponding increases in MnSO4 concentration from 0 to 33.8 microns and then decreased at higher MnSO4 concentrations. The stereochemical content of gamma-PGA was found to vary inversely with MnSO4 concentration, and ranged from 59 to 10% L-glutamate units for MnSO4 concentrations of 0 and 615 microns, respectively. For all of the MnSO4 concentrations investigated, the gamma-PGA molecular weights decreased rapidly as the gamma-PGA volumetric yield simultaneously increased for cultivation times from 24 to approximately 50 h. Mw and Mn values after approximately 50 h cultivation times, determined by gel permeation chromatography (GPC), were 1.3 to 1.6 and 0.5 to 0.8 million g mol-1, respectively. A complex gamma-PGA molecular weight distribution that appeared bimodal by GPC analysis due to the presence of a low-molecular-weight product fraction was observed in cultures containing 33.8 and 61.5 microns MnSO4 at extended cultivation times. A high-molecular-weight fraction and the unfractionated gamma-PGA sample from the 33.8 microns MnSO4 culture contained 13 +/- 4 and 30 +/- 1% L-repeat units, respectively. A relationship between the product molecular weight and its stereochemical composition was thus established.

摘要

地衣芽孢杆菌ATCC 9945A在摇瓶中培养,使用柠檬酸盐(12 g/L)、谷氨酸盐(20 g/L)和甘油(80 g/L)作为碳源用于细胞生长和γ-聚谷氨酸(γ-PGA)的生产。研究了培养基中硫酸锰(MnSO₄)浓度在0.0至615 μmol范围内的影响。到稳定期早期(24小时),所有MnSO₄浓度下的活细胞数量均从约10⁵个菌落形成单位(cfu)/ml增加到10⁹个cfu/ml。然而,50小时后,相对较低的MnSO₄浓度(0.615和0 μmol)下细胞活力迅速下降。相对于未添加MnSO₄的培养物,含有33.8和615 μmol MnSO₄的地衣芽孢杆菌培养物对碳源的利用率更高。例如,含有615 μmol MnSO₄的培养物分别利用了37%、54%和93%的谷氨酸盐、甘油和柠檬酸盐,而未添加MnSO₄的培养物分别利用了19%、10%和17%。随着MnSO₄浓度从0相应增加到33.8 μmol,γ-PGA的体积产率从约5 g/L增加到17 g/L,然后在较高MnSO₄浓度下下降。发现γ-PGA的立体化学含量与MnSO₄浓度成反比,MnSO₄浓度为0和615 μmol时,L-谷氨酸单元分别为59%和10%。对于所有研究的MnSO₄浓度,在24至约50小时的培养时间内,随着γ-PGA体积产率同时增加,γ-PGA分子量迅速下降。培养约50小时后,通过凝胶渗透色谱(GPC)测定的Mw和Mn值分别为130万至160万g/mol和50万至80万g/mol。在延长培养时间的含有33.8和61.5 μmol MnSO₄的培养物中,通过GPC分析观察到由于存在低分子量产物部分而呈现双峰的复杂γ-PGA分子量分布。来自33.8 μmol MnSO₄培养物的高分子量部分和未分级的γ-PGA样品分别含有13±4%和30±1%的L-重复单元。由此建立了产物分子量与其立体化学组成之间的关系。

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