功能強大、操作最簡便、發(fā)表文獻超多的葉綠素熒光成像系統(tǒng)
突變株快速篩選的強大工具
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MAXI版本，成像面積11×15 cm） 藍光版，450 nm，測葉片和真核藻類 紅光版，620 nm，測藍藻和真核藻類 可測量96孔板，平板，384點藻斑 | MINI版本，成像面積2.4×3.2 cm 藍光版，460 nm，測量葉片和真核藻類 紅光版，620 nm，測量葉片和藍藻 GFP版，480 nm，測量綠色熒光蛋白 | MICROSCOPY版本 藍光版：470 nm 紅光版：625nm RGB版：RGB光源 |
M-IMAGING-PAM是一套主機可分別接多個成像單元的葉綠素熒光成像系統(tǒng)，如MAXI成像單元，MINI成像單元以及搭載顯微鏡的MICROSCOPY成像單元。不同的成像單元適用于不同的應用場景，MAXI成像單元主要在實驗室內(nèi)使用，MINI成像單元可以帶到野外現(xiàn)場使用，MICROSCOPY成像單元可以用于組織或藻類單細胞測量。
每個成像單元有藍光和紅光兩個類型的光源區(qū)分，它們的區(qū)別在于藍光版主要用于高等植物和真核藻類的測量，而紅光版可以用于藍藻或藍藻共生的生物結(jié)皮，地衣測量。除此之外，MINI成像單元還有一個單獨的GFP版本，可以用于檢測遺傳標簽表達的GFP熒光蛋白。MICROSCOPY成像單元的RGB光源可以用于藻類種群信號解卷積，進行單細胞藻類分類。
M-IMAGING-PAM充分考慮了葉綠素熒光成像系統(tǒng)設計的基本原則：測量光強度足夠低的情況下最大限度的保證了有效成像面積內(nèi)的光場均勻性(最大差異小于2-7%)。廣場均勻的基礎上，M-IMAGING-PAM還充分考慮了絕大部分研究的需求，光化光和飽和脈沖強度均可滿足所有物種測量的基本要求。
M-IMAGING-PAM葉綠素熒光成像系統(tǒng)于2003年問世。時至今日，累計發(fā)表文獻4000多篇，光合作用文獻數(shù)據(jù)庫收錄2283篇，是發(fā)表文獻最多的PAM型號。近五年，每年都有超過200篇文獻發(fā)表。發(fā)文質(zhì)量高，其中不乏Nature，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(詳見附錄)。
M-IMAGING-PAM是葉綠素熒光成像系統(tǒng)的典范，不是所有的葉綠素熒光成像系統(tǒng)都叫M-IMAGING-PAM。
主要功能
原位測量：活體葉綠素熒光成像，直觀顯示樣品光合作用差異，可導出熒光參數(shù)彩色圖像。
成像功能：對Ft、Fo、Fm、Fv/Fm、F、Fm’、Y(II)、Y(NO)、Y(NPQ)、NPQ、qN、qP、qL、ETR、Abs.、NIR、Red、Inh等至少18種參數(shù)進行成像分析。測定調(diào)節(jié)性能量耗散Y(NPQ)，反映植物光保護能力，測定非調(diào)節(jié)性能量耗散Y(NO)，反映植物光損傷程度。
誘導曲線測量：手動和自動兩種模式。手動和自動模式下均可隨時更改誘導曲線的光化光強度，自動程序可測量熒光誘導曲線、誘導曲線+暗弛豫。測量過程中能自動分析和記錄所有熒光參數(shù)的變化趨勢。
光曲線測量：20個光梯度，可隨意設置光曲線步數(shù)，可測量滯后光曲線。
吸光系數(shù)測量功能：快速測量葉片的吸光系數(shù)。吸光系數(shù)測量光源： 16個紅光（660 nm）和16個近紅外（780 nm）LED，用于測量植物葉片或藻類樣品PAR吸光系數(shù)。
AOI功能：圓形，矩形，多邊形，增加，刪除，編輯，顯示/隱藏，填充，重置?？稍跍y量前或測量后任意選擇感興趣的區(qū)域（AOI），程序?qū)⒆詣訉x擇的AOI的數(shù)據(jù)進行變化趨勢分析，并在報告文件中顯示相關AOI的數(shù)據(jù)。所有報告文件中顯示的數(shù)據(jù)都可導出到EXCEL文件中。
時鐘重復：間隔可以在5秒和3600秒內(nèi)設置，重復指令：SAT.Pulse、AL、AL+Y和Ft。
腳本定制：48條模塊化腳本語句，可以完成一些非標準化的自定義實驗流程，如光周期震蕩實驗。
成像異質(zhì)性分析功能：對任意參數(shù)任意時間的成像，可在圖像上任意選取兩點，軟件自動對兩點間的數(shù)據(jù)進行橫向異質(zhì)性分析，并可導出到EXCEL文件中。
成像數(shù)據(jù)范圍分析功能：對任意參數(shù)任意時間的成像，可分析任意兩個熒光數(shù)值之間有多少個像素點，多少面積（cm2）。
突變株篩選功能：可跟據(jù)成像結(jié)果快速篩選光合、產(chǎn)氫/油、抗逆（抗鹽、抗旱、抗病等）等突變株。
微藻毒理研究功能：可同時測量96個微藻樣品（對照和處理組）的光合活性，軟件自動給出處理組樣品相對于對照組的光合抑制百分比。
成像參數(shù)
Fo, Fm, F, Ft, Fm', Fv/Fm, Y(II), qL, qP, qN, NPQ, Y(NPQ), Y(NO), ETR, Abs, NIR, Red, Inh等。
應用領域
光合作用研究：可以在完全相同的條件下同時對大量樣品進行成像
植物病理學：病斑部位（包括肉眼不可見時）成像以及病斑擴散的時空動力學
植物脅迫生理學：肉眼不可見脅迫損傷的早期檢測
遺傳育種：出苗后大規(guī)模快速篩選高光合/抗旱/抗熱/抗凍/抗病等植株
突變株篩選：快速篩選模式植物的光合突變株、抗逆突變株、產(chǎn)氫微藻突變株等
微藻毒理學：不同毒物濃度多個重復的樣品一次測完，軟件自動計算抑制比率
分子生物學：宏觀水平上檢測樣品的綠色熒光蛋白（GFP）熒光
其它多種擴展研究
擴展功能
IMAGIING-PAM與GFS-3000聯(lián)用
 | 模式一：MAXI-探頭與GFS-3000聯(lián)用，在10 cm x 13 cm的面積上同步測量氣體交換與熒光成像。 模式二：MINI-探頭與GFS-3000聯(lián)用，在2 cm x 3.2 cm的面積上同步測量氣體交換與熒光成像。 模式三：MINI-探頭與GFS-3000和擬南芥葉室聯(lián)用，實現(xiàn)擬南芥整株的同步測量（氣體交換與熒光成像）。 |
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Phenoplate：MAXI-IMAGIING-PAM與熱循環(huán)儀聯(lián)用
Phenoplate方法集成了Maxi-Imaging-PAM和熱循環(huán)儀，可在葉綠素a熒光測量之前、期間和之后對溫度進行快速動態(tài)控制。它可以在動態(tài)控制的熱環(huán)境中同時評估多達384個樣品的光系統(tǒng)II效率(Y(II))和非光化學淬滅(NPQ)。在本文中，我們展示了如何利用這一簡單的系統(tǒng)來詳細描述光合作用&光強&溫度之間在電子轉(zhuǎn)移率(ETR)和非光化學淬滅(NPQ)方面的關系。
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應用案例
突變株的快速篩選
MAXI-IMAGING-PAM特別適合對幼苗、愈傷組織、微藻等進行突變株的快速篩選，適合于與光合突變株、抗逆（抗旱、抗鹽、抗病等）突變株、產(chǎn)油/氫突變株等的快速篩選。
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| 突變株篩選案例：國內(nèi)某客戶使用384藻斑點篩選的衣藻突變株（左：Fo成像；右：Fv/Fm成像） |
環(huán)境對光合生物的影響
高溫，干旱，鹽分等環(huán)境條件會對光合生物產(chǎn)生非生物脅迫，影響光合作用正常進行。Fv/Fm作為光系統(tǒng)II最大光化學轉(zhuǎn)化效率常被用來指示脅迫對光合生物影響的程度，具有非常廣泛的應用。
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環(huán)境對光合生物的影響案例：全球變暖對珊瑚共生蟲黃藻光合能力的影響。
光合生物對環(huán)境的自我適應與調(diào)節(jié)
自然界中的植物通常都能很好地應對環(huán)境變化帶來的傷害，因為它們已經(jīng)進化出了敏銳的應對機制。非光化學淬滅可以將過剩的激發(fā)能耗散為熱量在其中起到了非常重要的作用。NPQ作為表征非光化學淬滅的熒光參數(shù)，在研究光下和暗弛豫階段的能量分配中被廣泛使用，具有非常重要的意義。
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光合生物對環(huán)境的自我適應與調(diào)節(jié)案例：擬南芥短鏈脫氫酶-還原酶突變體光保護能力研究
產(chǎn)地：德國WALZ
高分文獻目錄
數(shù)據(jù)來源：光合作用文獻Endnote數(shù)據(jù)庫
原始數(shù)據(jù)來源：Google Scholar
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