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JPH0695072B2 - Microbial activity measuring device - Google Patents
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JPH0695072B2 - Microbial activity measuring device - Google Patents

Microbial activity measuring device

Info

Publication number
JPH0695072B2
JPH0695072B2 JP63076849A JP7684988A JPH0695072B2 JP H0695072 B2 JPH0695072 B2 JP H0695072B2 JP 63076849 A JP63076849 A JP 63076849A JP 7684988 A JP7684988 A JP 7684988A JP H0695072 B2 JPH0695072 B2 JP H0695072B2
Authority
JP
Japan
Prior art keywords
optical filter
lens device
optical
excitation light
lens
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP63076849A
Other languages
Japanese (ja)
Other versions
JPH01250042A (en
Inventor
功一 堀内
初男 四元
由美子 ▲吉▼村
建樹 小沢
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Electric Corp
Original Assignee
Mitsubishi Electric Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP63076849A priority Critical patent/JPH0695072B2/en
Publication of JPH01250042A publication Critical patent/JPH01250042A/en
Publication of JPH0695072B2 publication Critical patent/JPH0695072B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/6486Measuring fluorescence of biological material, e.g. DNA, RNA, cells
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/645Specially adapted constructive features of fluorimeters
    • G01N21/6456Spatial resolved fluorescence measurements; Imaging
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/30Fuel from waste, e.g. synthetic alcohol or diesel

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Processing Of Solid Wastes (AREA)
  • Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
  • Treatment Of Sludge (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、有機性廃棄物、具体的には食品加工工場排
水、下水、有機汚泥、厨芥などを醗酵させてメタンガス
を生成するプロセス等におけるメタン生成菌数あるいは
その活性を計測する微生物活性計測装置に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention relates to a process for producing methane gas by fermenting organic waste, specifically, wastewater from a food processing factory, sewage, organic sludge, kitchen waste, etc. The present invention relates to a microbial activity measuring device for measuring the number of methanogenic bacteria or its activity.

〔従来の技術〕[Conventional technology]

従来、この種の計測装置として第4図に示すものがある
(特願昭61−14850号参照)。図において、8は被検体
としての微生物を含む懸濁液、24は懸濁液8を計測器ま
で導くための導管、25は計測時に懸濁液8を固定するた
めの手段であり、この場合はプランジャーで押さえ付け
固定するタイプのものを示している。26は集光器10で集
光された励起光を懸濁液8に照射し、同懸濁液8の発す
る螢光を導管24の外部で取り出すためのカバーグラスで
ある。
Conventionally, there is a measuring device of this type shown in FIG. 4 (see Japanese Patent Application No. 61-14850). In the figure, 8 is a suspension containing microorganisms as an analyte, 24 is a conduit for guiding the suspension 8 to a measuring instrument, and 25 is a means for fixing the suspension 8 at the time of measurement. Shows the type of pressing and fixing with a plunger. Reference numeral 26 is a cover glass for irradiating the suspension 8 with the excitation light condensed by the condenser 10 and extracting the fluorescence emitted from the suspension 8 outside the conduit 24.

次に動作について説明する。Next, the operation will be described.

導管24を通して送られてきた微生物を含む懸濁液8はプ
ランジャー25によってカバーグラス26とプランジャー25
の間に挟みこまれ、固定される。この時、光源2より発
し、光フィルタ12によって特定波長領域に限定され、集
光器10によって集光された励起光はカバーグラス26を通
して、固定されている微生物を含む懸濁液8に照射され
る。固定されている懸濁液8はこの励起光を受けて螢光
を発する。この螢光はカバーグラス26を介して導管24の
外部に取り出され、光フィルタ16によって特定波長範囲
に限定され、その後レンズ光学系20で拡大され、カメラ
21で螢光画像として取得され、信号線23を介して画像処
理装置22へ送られる。同画像処理装置22では、画像処理
を行ってメタン生成菌以外の異物に基づく螢光画像を排
除した後、メタン生成菌に基づく螢光画像からメタン生
成菌濃度あるいはメタン生成菌活性を算出する。
The suspension 8 containing microorganisms sent through the conduit 24 is covered by the plunger 25 with the cover glass 26 and the plunger 25.
It is sandwiched between and fixed. At this time, the excitation light emitted from the light source 2, limited to a specific wavelength region by the optical filter 12, and condensed by the condenser 10 is applied to the suspension 8 containing the fixed microorganisms through the cover glass 26. It The fixed suspension 8 receives this excitation light and emits fluorescence. This fluorescent light is taken out of the conduit 24 through the cover glass 26, limited to a specific wavelength range by the optical filter 16, and then enlarged by the lens optical system 20 to be used by the camera.
The fluorescence image is acquired at 21 and sent to the image processing device 22 via the signal line 23. The image processing device 22 performs image processing to eliminate a fluorescent image based on a foreign substance other than methanogenic bacteria, and then calculates a methanogenic bacterial concentration or a methanogenic bacterial activity from the fluorescent image based on the methanogenic bacteria.

〔発明が解決しようとする課題〕[Problems to be Solved by the Invention]

従来の微生物活性計測装置は以上のように構成されてい
るので、醗酵槽の培養液を微生物活性計測装置までひい
てこなければならず、採取機構が複雑になるという問題
点があった。
Since the conventional microbial activity measuring device is configured as described above, there is a problem in that the culture solution in the fermenter has to be drawn to the microbial activity measuring device, and the collection mechanism becomes complicated.

この発明は上記のような問題点を解消するためになされ
たもので、少なくとも微生物活性計測装置の光学系を醗
酵槽内に浸漬し、醗酵槽中の懸濁液の採取手段を設ける
必要のないメタン生成菌計測装置を提供することを目的
としている。
The present invention has been made to solve the above problems, at least the optical system of the microbial activity measuring device is immersed in the fermentation tank, it is not necessary to provide a means for collecting the suspension in the fermentation tank It is intended to provide a methanogen measuring device.

〔課題を解決するための手段〕[Means for Solving the Problems]

第1の発明に係る微生物活性計測装置は、励起光の照射
法に工夫をして、少なくとも微生物活性計測装置の励起
光用光学系とカメラ用光学系とを醗酵槽内に浸漬し、か
つ励起光用光学系の第1の光フィルタ・レンズ機器の光
軸を垂直に、かつ上記励起光の光束が上記第2の機器の
レンズの焦点を中心に第2の光フィルタ・レンズ機器の
光軸方向に±50μmの範囲で、しかも第2の光フィルタ
・レンズ機器の光軸の直交方向に対して該第2の光フィ
ルタ・レンズ機器のカメラ撮影光束径よりも広い範囲を
通過するように配置したものである。
The microbial activity measuring apparatus according to the first invention is devised in a method of irradiating excitation light, and at least the excitation light optical system and the camera optical system of the microbial activity measuring apparatus are immersed in a fermenter and excited. The optical axis of the first optical filter / lens device of the optical system for light is vertical, and the luminous flux of the excitation light is centered around the focus of the lens of the second device. In the direction of ± 50 μm, and arranged so as to pass through a range wider than the diameter of the light beam photographed by the camera of the second optical filter / lens device in the direction orthogonal to the optical axis of the second optical filter / lens device. It was done.

第2の発明に係る微生物活性計測装置は、少なくとも微
生物活性計測装置の励起光用光学系とカメラ用光学系を
醗酵槽内に浸漬し、かつ励起光用光学系の第1の光フィ
ルタ・レンズ機器の光軸とカメラ用光学系の第2の光フ
ィルタ・レンズ機器の光軸を一致させ、上記第1の機器
の先端の面と上記第2の機器の先端部分の間隔が、該第
2の機器の焦点距離分だけあるように設けたものであ
る。
A microbial activity measuring apparatus according to a second aspect of the present invention is such that at least an excitation light optical system and a camera optical system of the microbial activity measuring apparatus are immersed in a fermentation tank, and a first optical filter / lens of the excitation light optical system. The optical axis of the device and the optical axis of the second optical filter / lens device of the camera optical system are aligned, and the distance between the tip surface of the first device and the tip portion of the second device is equal to that of the second device. It is provided so that there is only the focal length of the device.

〔作用〕[Action]

この発明の微生物活性計測装置においては、醗酵槽の培
養液を微生物活性計測装置までひいてこなくてもよく、
複雑な採取機構がなくなり操作が簡単で、かつ第1,第2
の光フィルタ・レンズ機器の先端部分を限定しているの
で不要な部分からの光がカメラ用光学系に入らない。
In the microbial activity measuring device of the present invention, it is not necessary to pull the fermentation broth to the microbial activity measuring device,
No complicated collection mechanism, easy operation and 1st, 2nd
Since the tip part of the optical filter / lens device is limited, light from unnecessary parts does not enter the camera optical system.

〔実施例〕〔Example〕

以下、この発明の一実施例を図について説明する。 An embodiment of the present invention will be described below with reference to the drawings.

第1図は第1の発明の一実施例による微生物活性測定装
置を示す構成図、第2図は第1図の主要部分の拡大図で
あり、図1のA−A′断面を示したものである。図にお
いて、1は被検体である微生物を含む懸濁液8を内部に
保持する醗酵槽であり、第1の光フィルタ・レンズ機器
100と、それと光軸を直角に交わるように配置した第2
の光フィルタ・レンズ機器200とを内部に備えている。
2は光源であり、ここで発生した励起光は第2の光フィ
ルタ・レンズ機器200の焦点を中心に第2の光フィルタ
・レンズ機器200の光軸方向に±50μmの範囲で、かつ
第2の光フィルタ・レンズ機器200の光軸の直交方向に
対して第2の光フィルタ・レンズ機器200のカメラ撮影
光束径よりも若干大きな範囲に第1の光フィルタ・レン
ズ機器100を介して供給される。21は第2の光フィルタ
・レンズ機器200と光学的に接続された高感度ビデオカ
メラで信号線23を通して画像処理装置22に接続されてい
る。また、第2図において、100aは第2の光フィルタ・
レンズ機器200前方の励起光通過領域を示しており、101
は第2の光フィルタ・レンズ機器200の焦点である。
FIG. 1 is a block diagram showing a microbial activity measuring apparatus according to an embodiment of the first invention, and FIG. 2 is an enlarged view of a main part of FIG. 1, showing a cross section taken along the line AA 'of FIG. Is. In the figure, reference numeral 1 is a fermenter for holding therein a suspension 8 containing a microorganism as a test substance, and a first optical filter / lens device.
100 and the second one arranged so that the optical axis and the optical axis intersect at a right angle
The optical filter / lens device 200 of FIG.
Reference numeral 2 denotes a light source, and the excitation light generated here is within a range of ± 50 μm in the optical axis direction of the second optical filter / lens device 200 with the focus of the second optical filter / lens device 200 as the center, and Is supplied via the first optical filter / lens device 100 to a range slightly larger than the camera photographing light flux diameter of the second optical filter / lens device 200 in the direction orthogonal to the optical axis of the optical filter / lens device 200. It Reference numeral 21 is a high-sensitivity video camera optically connected to the second optical filter / lens device 200, and is connected to the image processing device 22 through a signal line 23. In FIG. 2, 100a is a second optical filter
The excitation light passage region in front of the lens device 200 is shown, and 101
Is the focal point of the second optical filter / lens device 200.

次に動作について説明する。Next, the operation will be described.

第1の光フィルタ・レンズ機器100の先端から出た光束
は、第2の光フィルタ・レンズ機器200の焦点を中心に
第2の光フィルタ・レンズ機器200の光軸方向に±50μ
mの範囲で、かつ第2の光フィルタ・レンズ機器200の
光軸の直交方向に対して第2の光フィルタ・レンズ機器
200のカメラ撮影光束径の範囲内の微生物を含む懸濁液
8を励起して、メタン生成菌に蛍光を発生させる。この
光束によって励起させられ高純度ビデオカメラ21で撮像
されるメタン生成菌は、第2の光フィルタ・レンズ機器
200の焦点を中心に第2の光フィルタ・レンズ機器200の
光軸方向に±50μmの範囲であり、また第2の光フィル
タ・レンズ機器200の光軸の直交方向に対しては第2の
光フィルタ・レンズ機器200のカメラ撮影光束径で限定
された範囲内にいるメタン生成菌のみであるから、その
測定領域の容積が簡単に測定できる。メタン生成菌より
発した螢光はカメラ21で螢光画像として取得され、信号
線23を介して画像処理装置22へ送られる。画像処理装置
22では、画像処理を行ってメタン生成菌以外の異物に基
づく螢光画像を排除した後、メタン生成菌に基づく螢光
画像と測定領域の容積からメタン生成菌濃度あるいはメ
タン生成菌活性を算定する。
The luminous flux emitted from the tip of the first optical filter / lens device 100 is centered on the focus of the second optical filter / lens device 200 and is ± 50 μ in the optical axis direction of the second optical filter / lens device 200.
The second optical filter / lens device in the range of m and in the direction orthogonal to the optical axis of the second optical filter / lens device 200.
The suspension 8 containing microorganisms within the range of the 200 photographed light flux diameter is excited to cause the methanogen to emit fluorescence. The methanogen that is excited by this luminous flux and imaged by the high-purity video camera 21 is the second optical filter / lens device.
The range is ± 50 μm in the optical axis direction of the second optical filter / lens device 200 with the focus of 200 as the center, and the second optical filter / lens device 200 has a second range in the direction orthogonal to the optical axis of the second optical filter / lens device 200. Since only methanogens within the range limited by the camera photographing light flux diameter of the optical filter / lens device 200 are present, the volume of the measurement area can be easily measured. The fluorescence emitted from the methanogen is acquired by the camera 21 as a fluorescence image and sent to the image processing device 22 via the signal line 23. Image processing device
In 22, the image processing is performed to eliminate the fluorescent images based on foreign substances other than methanogens, and then the methanogenic concentration or methanogenic activity is calculated from the fluorescent images based on methanogenic bacteria and the volume of the measurement area. .

また第3図は第2の発明の一実施例によるメタン生成菌
計測装置の主要部分の拡大図である。
Further, FIG. 3 is an enlarged view of the main part of the methanogen measuring device according to one embodiment of the second invention.

上記第1の発明の実施例では第1の光フィルタ・レンズ
機器100と第2の光フィルタ・レンズ機器200とはその光
軸を直交させたが、本実施例では第1の光フィルタ・レ
ンズ機器100と第2の光フィルタ・レンズ機器200とはそ
の光軸を一致させ、かつ励起光を出す機器の先端の面と
第2の光フィルタ・レンズ機器200の先端部分の間隔を
第2の光フィルタ・レンズ機器200の焦点距離分Aだけ
開けて醗酵槽1内に設置し、画像処理装置22でピントの
ぼけた画像は測定しないように設定したものである。本
実施例においても、測定領域の容積は〔光束断面積×焦
点の合う距離〕で求められ、上記実施例と同様の効果を
得ることができる。
In the embodiment of the first invention, the optical axes of the first optical filter / lens device 100 and the second optical filter / lens device 200 are made orthogonal to each other, but in the present embodiment, the first optical filter / lens device is used. The optical axes of the device 100 and the second optical filter / lens device 200 are aligned with each other, and the distance between the end surface of the device that emits the excitation light and the end portion of the second optical filter / lens device 200 is set to the second distance. The optical filter / lens device 200 is opened by the focal length A and installed in the fermenter 1, and the image processing device 22 is set so as not to measure a blurred image. Also in this embodiment, the volume of the measurement region is obtained by [light flux cross-sectional area × focus distance], and the same effect as in the above embodiment can be obtained.

このように、上記2つの実施例装置では醗酵槽中の微生
物を含む懸濁液を採取せずに懸濁液中のメタン生成菌濃
度及びメタン生成菌活性を測定できるようにしたので、
装置が安価にでき、さらに複雑な採取機構を設けなくて
もよく、操作が簡単になるものである。
As described above, in the above-mentioned two embodiment devices, the concentration of methanogenic bacteria and the activity of methanogenic bacteria in the suspension can be measured without collecting the suspension containing the microorganisms in the fermenter.
The device can be made inexpensive, and a complicated sampling mechanism need not be provided, which simplifies the operation.

〔発明の効果〕〔The invention's effect〕

以上のように本発明の微生物活性計測装置によれば、励
起光用光学系の第1の光フィルタ・レンズ機器の光軸と
カメラ用光学系の第2の光フィルタ・レンズ機器の光軸
を一致あるいは垂直になるようにし、しかも両光フィル
タ・レンズ機器の先端部分の間隔を限定して醗酵槽内に
設けるように構成したので不要な部分からの光がカメラ
用光学系に入らず、測定精度が向上し、また醗酵槽中の
懸濁液を採取せずに懸濁液中のメタン生成菌濃度および
活性を測定できるので複雑な採取機構を設ける必要がな
く操作が簡単になり、さらに装置が安価に提供できると
いう効果がある。
As described above, according to the microbial activity measuring apparatus of the present invention, the optical axis of the first optical filter / lens device of the optical system for excitation light and the optical axis of the second optical filter / lens device of the optical system for camera are set. It is designed to be aligned or vertical, and the distance between the tips of both optical filters and lens devices is limited so that it is installed inside the fermentor, so light from unnecessary parts does not enter the camera optical system and measurement The accuracy is improved, and the concentration and activity of methanogens in the suspension can be measured without collecting the suspension in the fermentor, which simplifies the operation without the need for a complicated collection mechanism. Can be provided at low cost.

【図面の簡単な説明】[Brief description of drawings]

第1図は第1の発明の一実施例による微生物活性計測装
置を示す構成図、第2図は第1図の微生物活性計測装置
の主要部分の拡大図、第3図は第2の発明の一実施例に
よる微生物活性計測装置の主要部分の拡大図、第4図は
従来の微生物活性計測装置の構成図である。 1は醗酵槽、2は光源、8は懸濁液、10は集光器、12,1
6は光フィルタ、20はレンズ光学系、21はカメラ、22は
画像処理装置、23は信号線、24は導管、25はプランジャ
ー、26はカバーグラス、100は第1の光フィルタ・レン
ズ機器、200は第2の光フィルタ・レンズ機器である。 なお図中同一符号は同一又は相当部分を示す。
FIG. 1 is a block diagram showing a microbial activity measuring apparatus according to an embodiment of the first invention, FIG. 2 is an enlarged view of a main part of the microbial activity measuring apparatus of FIG. 1, and FIG. 3 is a second invention. FIG. 4 is an enlarged view of the main part of the microbial activity measuring apparatus according to one embodiment, and FIG. 4 is a block diagram of a conventional microbial activity measuring apparatus. 1 fermentor, 2 light source, 8 suspension, 10 light collector, 12,1
6 is an optical filter, 20 is a lens optical system, 21 is a camera, 22 is an image processing device, 23 is a signal line, 24 is a conduit, 25 is a plunger, 26 is a cover glass, and 100 is a first optical filter / lens device. , 200 is a second optical filter / lens device. The same reference numerals in the drawings indicate the same or corresponding parts.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 小沢 建樹 兵庫県尼崎市塚口本町8丁目1番1号 三 菱電機株式会社応用機器研究所内 (56)参考文献 特開 昭62−174636(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Kenki Ozawa 8-1-1 Tsukaguchihonmachi, Amagasaki-shi, Hyogo Sanryo Electric Co., Ltd. Applied Equipment Research Laboratory (56) Reference JP-A-62-174636 (JP, A) )

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】微生物を含有する被検体を含む醗酵槽と、 上記醗酵槽内に設けられ、上記被検体に所定の波長範囲
の励起光を照射する励起光用光学系と、 上記醗酵槽内に設けられ、上記被検体が上記励起光の照
射を受けて発する螢光のうち所定の波長範囲の螢光を螢
光画像として取得するカメラ用光学系とを備え、 上記励起光用光学系は第1の光フィルタ・レンズ機器
を、上記カメラ用光学系は第2の光フィルタ・レンズ機
器を有し、該両光フィルタ・レンズ機器は第2の光フィ
ルタ・レンズ機器の光軸が第1の光フィルタ・レンズ機
器の光軸と直交し、上記励起光の光束が第2の光フィル
タ・レンズ機器の焦点を中心に第2の光フィルタ・レン
ズ機器の光軸方向に±50μmの範囲で、かつ第2の光フ
ィルタ・レンズ機器の光軸の直交方向に対して該第2の
光フィルタ・レンズ機器のカメラ撮影光束径よりも広い
範囲を通過するように設けられていることを特徴とする
微生物活性計測装置。
1. A fermentation tank containing an analyte containing a microorganism, an optical system for excitation light provided in the fermentation tank for irradiating the analyte with excitation light in a predetermined wavelength range, and the inside of the fermentation tank. Provided in, the subject comprises a camera optical system to obtain as a fluorescence image fluorescence of a predetermined wavelength range of fluorescence emitted by receiving the irradiation of the excitation light, the optical system for excitation light, A first optical filter / lens device, the camera optical system has a second optical filter / lens device, and the both optical filters / lens devices have a second optical filter / lens device with an optical axis being first. Is orthogonal to the optical axis of the optical filter / lens device, and the luminous flux of the excitation light is within a range of ± 50 μm in the optical axis direction of the second optical filter / lens device around the focus of the second optical filter / lens device. And in the direction orthogonal to the optical axis of the second optical filter / lens device. Microbial activity measuring apparatus characterized by being arranged to pass through a wider range than the camera shooting beam diameter of the optical filter lens device of the second Te.
【請求項2】微生物を含有する被検体を含む醗酵槽と、 上記醗酵槽内に設けられ、上記被検体に所定の波長範囲
の励起光を照射する励起光用光学系と、 上記醗酵槽内に設けられ、上記被検体が上記励起光の照
射を受けて発する螢光のうち所定の波長範囲の螢光を螢
光画像として取得するカメラ用光学系とを備え、 上記励起光用光学系は第1の光フィルタ・レンズ機器
を、上記カメラ用光学系は第2の光フィルタ・レンズ機
器を有し、該両光フィルタ・レンズ機器は第2の光フィ
ルタ・レンズ機器の光軸と、第1の光フィルタ・レンズ
機器の光軸が一致し、かつ第1の光フィルタ・レンズ機
器の先端の面と第2の光フィルタ・レンズ機器の先端部
分の間隔が、第2の光フィルタ・レンズ機器の焦点距離
分だけあるように設けられていることを特徴とする微生
物活性計測装置。
2. A fermentation tank containing an analyte containing a microorganism, an optical system for excitation light which is provided in the fermentation tank and irradiates the analyte with excitation light in a predetermined wavelength range, and the inside of the fermentation tank. Provided in, the subject comprises a camera optical system to obtain as a fluorescence image fluorescence of a predetermined wavelength range of fluorescence emitted by receiving the irradiation of the excitation light, the optical system for excitation light, A first optical filter / lens device, the camera optical system has a second optical filter / lens device, and both optical filter / lens devices have an optical axis of the second optical filter / lens device; The optical axis of the first optical filter / lens device is the same, and the distance between the end surface of the first optical filter / lens device and the end portion of the second optical filter / lens device is the second optical filter / lens. That there is only the focal length of the device Microbial activity measuring device for the butterflies.
JP63076849A 1988-03-30 1988-03-30 Microbial activity measuring device Expired - Fee Related JPH0695072B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63076849A JPH0695072B2 (en) 1988-03-30 1988-03-30 Microbial activity measuring device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63076849A JPH0695072B2 (en) 1988-03-30 1988-03-30 Microbial activity measuring device

Publications (2)

Publication Number Publication Date
JPH01250042A JPH01250042A (en) 1989-10-05
JPH0695072B2 true JPH0695072B2 (en) 1994-11-24

Family

ID=13617104

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63076849A Expired - Fee Related JPH0695072B2 (en) 1988-03-30 1988-03-30 Microbial activity measuring device

Country Status (1)

Country Link
JP (1) JPH0695072B2 (en)

Also Published As

Publication number Publication date
JPH01250042A (en) 1989-10-05

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