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雙通道調制葉綠素熒光儀DUAL-PAM-100
日期:2025-03-17 16:31:27

同步測量PSII活性(葉綠素熒光)和PSI活性(P700氧化還原)

擴展P515/535模塊可測量質子動力勢(pmf)組分:跨膜質子梯度ΔpH和跨膜電位ΔΨ

擴展NADPH/9-AA模塊可以測量NADPH熒光和9-AA熒光

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高等植物測量模式

藻液/懸浮液測量模式

標準版的雙通道調制葉綠素熒光儀DUAL-PAM-100可同時測量光系統(tǒng)II(PSII)葉綠素熒光(Fluo)和光系統(tǒng)I(PSI)氧化還原導致的近紅外差示吸收(P700/P700+)。自2006年DUAL-PAM-100問世以來,它就成為了PSII和PSI活性同步測量的黃金標準。

雙通道調制葉綠素熒光儀DUAL-PAM-100可以用于植物葉片原位活體測量,只需要將葉片夾在激發(fā)和檢測單元中間即可,幾乎不需要任何前處理。此外,它也可以測量提取的完整葉綠體或類囊體懸浮液,微藻懸浮液。只需將裝有樣品(1.4mL)的石英杯放置在特制光學單元中間的孔內,蓋上蓋子即可。如果您在測量過程中需要往懸浮液內加藥劑,可以從蓋子中間的微小開孔插入注射器針頭,添加藥劑。對于易沉降的樣品可以使用磁力攪拌器攪拌。

雙通道調制葉綠素熒光儀DUAL-PAM-100除了標準激發(fā)和檢測單元配置外,還有3個擴展選項:

雙通道調制葉綠素熒光儀DUAL-PAM-100發(fā)表文獻數(shù)量多,僅光合作用文獻數(shù)據(jù)庫收錄的就有1680多篇,近五年,每年都有近200篇文獻發(fā)表。發(fā)文質量高,其中不乏Molecular Plant,Nature Plants,Nature Communications,The Plant Cell,PNAS,New Phytologist,Plant Physiology,The Plant Journal等植物學領域的專業(yè)高分雜志文章。

DUAL-PAM-100主要功能

DUAL-PAM-100測量數(shù)據(jù)

DUAL-PAM-100應用領域

DUAL-PAM-100軟件界面
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測量模式和分析模式選擇

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雙通道模式測量光設置

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同步測量PSI和PSII誘導曲線和暗弛豫

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同步測量PSI和PSII光響應曲線

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同時繪制兩條Poly_300ms的快相曲線

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測量系統(tǒng)間電子傳遞載體(PQ)庫

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測量520-550nm差示吸收研究ΔpH,ΔΨ,pmf

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NADPH模塊測量的NADP+還原曲線

DUAL-PAM-100可選附件

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P515/535

NADPH/9AA
3010-DUAL

1、擴展P515/535模塊,可測量跨類囊體膜的質子梯度ΔpH和跨膜電位ΔΨ,分析與電子傳遞耦合的跨類囊體膜質子轉移,質子動力勢pmf形成。
2、擴展NADPH/9-AA模塊,可測量NADP+的還原程度。
3、擴展3010-DUAL聯(lián)用葉室,可與GFS-3000光合儀組合,在可控條件(光照,溫度,濕度,CO2濃度)下同步測量氣體交換相關的CO2同化和電子傳遞相關的氧化還原。

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US-T

4、針對控制溫度測量的特殊實驗要求,您可以為DUAL-PAM-100懸浮樣品光學單元配置控溫模塊:A、循環(huán)水浴,需要用戶自備恒溫水浴裝置,只需將其通過軟件連接到控溫模塊即可;B、Pelletier控溫模塊,兼具加熱和制冷兩種模式,可直接裝在懸浮樣品光學單元頂部,探頭插入樣品即可。

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DUAL-DPD
DUAL-DPM

5、對于低濃度的葉綠體/類囊體/藻類懸浮液,熒光信號也會特別低。為了保證信號質量需要選用靈敏度更高的檢測器來記錄信號。A,光電二極管探測器單元DUAL-DPD的靈敏度比標準探頭提高了約10倍??梢赃M行樣品濃度低至5 μg Chl/L 的測量;B、光電倍增管探測器單元 DUAL-DPM的靈敏度比DUAL-DPD更高,可以非??煽康販y量葉綠素濃度低至 0.5 μg/L 的懸浮液。
DUAL-PAM-100與GFS-3000聯(lián)用

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DUAL-PAM-100

3010-DUAL
GFS-3000

3010-DUAL是專們?yōu)镈UAL-PAM-100與GFS-3000聯(lián)用而設計的特制氣體交換葉室。葉室由線性定位支架、溫度和PAR傳感器、風扇、導光桿、電子盒構成。同步測量時,葉片夾在葉室中間,DUAL-PAM-100提供測量需要的所有廣源。氣體交換由GFS-3000的紅外氣體分析器(IRGA)檢測,P700和葉綠素熒光由DUAL-PAM-100的檢測器測量。

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DUAL-PAM-100應用案例
案例1:中國農(nóng)業(yè)科學院作物科學研究所周文彬研究員課題組使用CRISPR-Cas9技術隨機編輯水稻中Rubisco的五個rbcS基因(OsrbcS1–5),產(chǎn)生一系列敲除突變體。以此來研究編碼RuBisCO小亞基(RbcS)的基因突變后對水稻光合作用的影響。研究發(fā)現(xiàn),水稻光合組織中最主要的rbcS基因OsrbcS2-5突變后,水稻在田間條件下的生長受抑制、抽穗延遲和產(chǎn)量降低,同時RuBisCO含量和活性降低,光合效率顯著降低。多個突變導致的遲緩表型更嚴重。本研究中,野生型和rbcs突變體水稻光系統(tǒng)I和光系統(tǒng)II葉綠素熒光光響應曲線通過DUAL-PAM-100雙通道葉綠素熒光儀完成,測量前暗適應30分鐘,設置一系列光梯度,每個光梯度照光30 s,然后施加一個200 ms的光強為20000 μmol·m-2·s-1的飽和脈沖。測量Y(I)、Y(II)、ETRI、ETRII、Y(ND)、Y(NA)等參數(shù)。
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Zhou, Y., et al. 2024. https://doi.org/10.1111/pbi.14535
案例2:英國謝菲爾德大學Matthew P Johnson課題組利用基于CRISPR/Cas9的基因編輯技術,在萊茵衣藻中構建了通過PSAF將FNR錨定于PSI的嵌合型突變體。以此來研究FNR定位對光合作用的影響。研究發(fā)現(xiàn),相較于野生型,嵌合突變體因NADPH還原速率降低導致光合生長受限、線性電子傳遞受阻,且PSI受體側限制增強。但該突變體同時表現(xiàn)出增強的跨膜質子梯度(ΔpH)和非光化學淬滅(NPQ),表明CET活性顯著提升。因此,將FNR錨定于PSI并未促進光合線性電子傳遞,反而通過犧牲線性電子傳遞與CO?固定效率優(yōu)先支持環(huán)式電子傳遞。這一發(fā)現(xiàn)揭示了FNR定位對光合電子流向分配的關鍵調控作用。
本研究中,葉綠素熒光與電子傳遞,使用IMAGING-PAM葉綠素熒光成像系統(tǒng)測定Fm、光響應曲線及誘導曲線,400 μL樣品,100 μg/mL葉綠素濃度,添加15% Ficoll(聚蔗糖);使用DUAL-PAM-100雙通道葉綠素熒光儀P515/535模塊檢測電致變色位移(ECS)。質子動力勢根據(jù)紅色光化光關閉后P515信號的衰減來計算,方法是對黑暗中的前300 ms進行單指數(shù)衰減,以確定信號衰減的跨度(ECSt);質子導度(gH+)是根據(jù)該衰減速率常數(shù)的倒數(shù)計算。質子通量(vH+)按ECSt×gH+計算;使用 DUAL-KLAS-NIR四通道動態(tài)LED陣列近紅外光譜儀以類似方法測量P700氧化。樣品葉綠素濃度100 μg/mL,添加10 μM DCMU和1 mM HA后進行測量前的暗適應。在502 μmol·m-2·s-1的紅色光化光照射10秒后,測量P700氧化的衰減(波長對840-965nm)。在光照結束時,使用200 ms的多周轉飽和閃光(MT)來測量P700氧化的最大值(Pm),并使用脈沖后最初的1.5秒曲線擬合非線性衰減函數(shù)來計算P700還原一階速率常數(shù)K;3、NADPH熒光,激發(fā)波長340 nm,檢測波長460 nm,光暗交替下測定動態(tài)變化。
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Emrich-Mills, T. Z., et al. 2025. https://doi.org/10.1093/plcell/koaf042
代表文獻

數(shù)據(jù)來源:光合作用文獻Endnote數(shù)據(jù)庫

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