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在指数生长后期,通过 Aureobasidium pullulans ipe-1 强化 β-聚(L:-苹果酸)的生产。

Intensification of β-poly(L: -malic acid) production by Aureobasidium pullulans ipe-1 in the late exponential growth phase.

机构信息

National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, People's Republic of China.

出版信息

J Ind Microbiol Biotechnol. 2012 Jul;39(7):1073-80. doi: 10.1007/s10295-012-1111-3. Epub 2012 Mar 7.

Abstract

β-Poly(malic acid) (PMLA) has attracted industrial interest because this polyester can be used as a prodrug or for drug delivery systems. In PMLA production by Aureobasidium pullulans ipe-1, it was found that PLMA production was associated with cell growth in the early exponential growth phase and dissociated from cell growth in the late exponential growth phase. To enhance PMLA production in the late phase, different fermentation modes and strategies for controlling culture redox potential (CRP) were studied. The results showed that high concentrations of produced PMLA (above 40 g/l) not only inhibited PMLA production, but also was detrimental to cell growth. Moreover, when CRP increased from 57 to 100 mV in the late exponential growth phase, the lack of reducing power in the broth also decreased PMLA productivity. PMLA productivity could be enhanced by repeated-batch culture to maintain cell growth in the exponential growth phase, or by cell-recycle culture with membrane to remove the produced PMLA, or by maintaining CRP below 70 mV no matter which kind of fermentation mode was adopted. Repeated-batch culture afforded a high PMLA concentration (up to 63.2 g/l) with a productivity of 1.15 g l(-1) h(-1). Cell-recycle culture also confirmed that PMLA production by the strain ipe-1 was associated with cell growth.

摘要

β-聚(苹果酸)(PMLA)因其可用作前药或药物传递系统而引起了工业界的兴趣。在出芽短梗霉ipe-1 生产 PMLA 时,发现 PLMA 的生产与早期指数生长期的细胞生长有关,而与晚期指数生长期的细胞生长无关。为了在后期提高 PMLA 的产量,研究了不同的发酵模式和控制培养氧化还原电位(CRP)的策略。结果表明,高浓度的 PMLA(高于 40 g/l)不仅抑制 PMLA 的生产,而且对细胞生长也有害。此外,当 CRP 在指数生长期后期从 57 增加到 100 mV 时,发酵液中缺乏还原能力也降低了 PMLA 的生产力。通过重复分批培养来维持细胞在指数生长期的生长,可以提高 PMLA 的生产力,或者通过膜循环培养来去除产生的 PMLA,或者通过将 CRP 保持在 70 mV 以下,无论采用哪种发酵模式,都可以提高 PMLA 的生产力。重复分批培养可获得高浓度的 PMLA(高达 63.2 g/l),产率为 1.15 g l(-1) h(-1)。细胞循环培养也证实了菌株 ipe-1 产生的 PMLA 与细胞生长有关。

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