目錄:北京易科泰生態(tài)技術(shù)有限公司>>植物類>>LED光源與植物生長箱>> 藻類培養(yǎng)系統(tǒng)
價格區(qū)間 | 面議 |
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FMT150藻類培養(yǎng)與在線監(jiān)測系統(tǒng)
——光氧細(xì)菌和藻類培養(yǎng)與狀態(tài)在線監(jiān)測的*結(jié)合
光養(yǎng)生物反應(yīng)器是指用于培養(yǎng)藻類、光養(yǎng)細(xì)菌等的技術(shù)系統(tǒng),一般由培養(yǎng)系統(tǒng)(如光、培養(yǎng)容器、溫度控制等)和監(jiān)測系統(tǒng)(如PH值等)組成,可分為開放式和封閉式。廣泛應(yīng)用于生物工程領(lǐng)域如食品、水產(chǎn)養(yǎng)殖、營養(yǎng)保健制劑、醫(yī)藥如抗體及抗腫瘤藥物等,生態(tài)環(huán)境工程領(lǐng)域如水體生態(tài)修復(fù)、CO2吸收、污水處理如重金屬吸收等,能源領(lǐng)域如微藻生物柴油等。同時,隨著碳排放的增加,海洋藻類對變化的響應(yīng)也逐漸成為光養(yǎng)生物反應(yīng)器應(yīng)用的重要領(lǐng)域。
FMT150藻類培養(yǎng)與在線監(jiān)測系統(tǒng)將生物反應(yīng)器與監(jiān)測儀器*地結(jié)合在一起,用于淡水、海水藻類和藍(lán)細(xì)菌(藍(lán)藻)等的模塊化精確光照培養(yǎng)與生理監(jiān)測。
FMT150可以通過控制單元(包括電腦與預(yù)裝軟件,軟件分為基本版與高級版)中用戶自定義程序動態(tài)自動改變培養(yǎng)條件并實時在線監(jiān)測培養(yǎng)條件與測量參數(shù)。光強(qiáng)、光質(zhì)、溫度和通入氣體的組分與流速都可以精確調(diào)控。加裝恒濁和恒化模塊后還可以調(diào)控培養(yǎng)基的pH值和濁度。FMT150可連接多達(dá)7個蠕動泵進(jìn)行不同恒化與pH條件培養(yǎng)。培養(yǎng)條件可以根據(jù)用戶自定義方案動態(tài)變化,既可以進(jìn)行恒定條件下的培養(yǎng),也可以一定的周期自動變化??刂茊卧赏瑫r控制多臺FMT150進(jìn)行同步實驗,保證不同處理實驗間的*性。
儀器內(nèi)置葉綠素?zé)晒鈨x和光密度計等。培養(yǎng)藻類的生長狀況由光密度計測定OD680和OD720實現(xiàn)實時監(jiān)控,并可以通過OD值監(jiān)測相對葉綠素濃度。葉綠素?zé)晒鈨x實時監(jiān)測Ft并可測定F0、Fm、Fm′和QY來反映培養(yǎng)藻類的光合生理狀態(tài)。
藻類培養(yǎng)系統(tǒng)應(yīng)用領(lǐng)域:
環(huán)境科學(xué)與環(huán)境工程——藻類的利用與有害控制
用于水體中水華和赤潮現(xiàn)象的模擬、預(yù)警防治研究,水體污染治理與生態(tài)修復(fù)研究如利用藻類進(jìn)行水體重金屬污染及面源污染的消納研究等,大氣污染生態(tài)修復(fù)研究如利用藻類對污染排放進(jìn)行吸收的研究等,及利用藻類吸收大氣二氧化碳的研究等等。
生態(tài)學(xué)與生態(tài)工程
海洋初級生產(chǎn)力研究,海洋碳循環(huán),浮游植物等光養(yǎng)生物生理生態(tài)研究,藻類對變化的響應(yīng)機(jī)制,生物圈模擬研究,水體生態(tài)修復(fù)研究等。
生物工程與生物醫(yī)學(xué)工程
用于藻類保健營養(yǎng)品的開發(fā)研究,藻類轉(zhuǎn)基因抗腫瘤藥物的開發(fā)研究,水產(chǎn)養(yǎng)殖藻類培養(yǎng)等等。
生物能源開發(fā)——向藻類要能源
地球上的石油、煤炭等常規(guī)能源面臨資源枯竭及環(huán)境污染、溫室氣體排放等嚴(yán)重問題,用玉米等糧食進(jìn)行生物柴油的開發(fā)一度引起的糧食危機(jī),目前上已將生物柴油的開發(fā)焦點轉(zhuǎn)向藻類,藻類獨居植物產(chǎn)油率。FMT150已成為歐美國家用于藻類生物能源培養(yǎng)研究的熱門設(shè)備。
藻類培養(yǎng)系統(tǒng)
主要特點:
技術(shù)參數(shù)指標(biāo)
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基礎(chǔ)版 | 高級版 |
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產(chǎn)地:歐洲
參考文獻(xiàn):
1. Light attenuation changes with photo-acclimation in a culture of Synechocystis sp. PCC 6803. Straka L, et al. 2017, Algal Research, DOI: 10.1016/j.algal.2016.11.024
2. Quantitating active Photosystem II reaction center content from fluorescence induction transients. Murphy CD, et al. 2017, Limnology and Oceanography: Methods, 15(1): 54-69
3. Comparative evaluation of phototrophic microtiter plate c*tion against laboratory-scale photobioreactors. Morschett H, et al. 2017, Bioprocess and Biosystems Engineering, 40(5): 663-673
4. Impaired mitochondrial transcription termination disrupts the stromal redox poise in Chlamydomonas. Uhmeyer A, et al. 2017, Plant Physiology, 174(3): 1399-1419
5. Interactive effects of nitrogen and light on growth rates and RUBISCO content of small and large centric diatoms. Li G, et al. 2017, Photosynthesis Research, 131(1): 93-103
6. A method to decompose spectral changes in Synechocystis PCC 6803 during light-induced state transitions. Acuña AM, et al. 2016, Photosynthesis Research, 130 (1) : 1-13
7. Comparison of D1´‐and D1‐containing PS II reaction centre complexes under different environmental conditions in Synechocystis sp. PCC 6803. Crawford TS, et al. 2016, Plant, Cell & Environment, 39(8): 1715-1726
8. The source of inoculum drives bacterial community structure in Synechocystis sp. PCC6803-based photobioreactors. Zevin AS, et al. 2016, Algal Research, 13: 109-115
9. Flow cytometry enables dynamic tracking of algal stress response: A case study using carotenogenesis in Dunaliella salina, Fachet M, et al. 2016, Algal Research, 13: 227-234
10. The nitrogen costs of photosynthesis in a diatom under current and future pCO2, G Li, et al. 2015, New Phytologist, 205(2): 533-543
11. Synechococcus elongatus UTEX 2973, a fast growing cyanobacterial chassis for biosynthesis using light and CO2. J Yu, et al. 2015, Sci Rep. 5: 8132.
12. Sustained circadian rhythms in continuous light in Synechocystis sp. PCC6803 growing in a well-controlled photobioreactor. P van Alphen, et al. 2015, PLoS ONE 10(6): e0127715.
13. Effects of phosphate limitation on soluble microbial products and microbial community structure in semi‐continuous Synechocystis‐based photobioreactors. AS Zevin, et al. 2015, Biotechnology and Bioengineering, 112(9): 1761-1769
14. C*tion of Nannochloropsis for eicosapentaenoic acid production in wastewaters of pulp and paper industry. A Polishchuk, et al. 2015, Bioresource Technology, 193: 469-476
15. Interactive effects of and light on growth rates and RUBISCO content of small and large centric diatoms. G Li, et al. 2015, Biogeosciences Discuss., 12: 16645-16672
16. The role of an electron pool in algal photosynthesis during sub-second light–dark cycling. C Vejrazka, et al. 2015, Algal Research, 12: 43-51
17. A dynamic growth model of Dunaliella salina: Parameter identification and profile likelihood analysis, M Fachet, et al. 2014, Bioresource Technology, 173: 21-31
18. Effects of light and circadian clock on growth and chlorophyll accumulation of Nannochloropsis gaditana, R Braun, et al. 2014, Journal of Phycology, 50(3): 515-525
19. Ultradian metabolic rhythm in the diazotrophic cyanobacterium Cyanothece sp. ATCC 51142, J ?ervený, et al. 2013, PNAS, 110(32): 13210-13215
20. Temperature-dependent growth rate and photosynthetic performance of Antarctic symbiotic alga Trebouxia sp. c*ted in a bioreactor, K Balarinová, et al. 2013, Czech polar reports, 3 (1): 19-27
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