CN1657605A - Method of increasing hydrogen releasing efficient of chlamydomonas - Google Patents
Method of increasing hydrogen releasing efficient of chlamydomonas Download PDFInfo
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- CN1657605A CN1657605A CN 200510011297 CN200510011297A CN1657605A CN 1657605 A CN1657605 A CN 1657605A CN 200510011297 CN200510011297 CN 200510011297 CN 200510011297 A CN200510011297 A CN 200510011297A CN 1657605 A CN1657605 A CN 1657605A
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- 239000001257 hydrogen Substances 0.000 title claims abstract description 75
- 229910052739 hydrogen Inorganic materials 0.000 title claims abstract description 75
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims abstract description 50
- 238000000034 method Methods 0.000 title claims abstract description 46
- 241000195585 Chlamydomonas Species 0.000 title claims abstract description 39
- 230000008569 process Effects 0.000 claims abstract description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 25
- 241000305071 Enterobacterales Species 0.000 claims description 20
- 241000588747 Klebsiella pneumoniae Species 0.000 claims description 16
- 241000349731 Afzelia bipindensis Species 0.000 claims description 12
- 241000588748 Klebsiella Species 0.000 claims description 11
- 201000008225 Klebsiella pneumonia Diseases 0.000 claims description 11
- 206010035717 Pneumonia klebsiella Diseases 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 11
- 241000588749 Klebsiella oxytoca Species 0.000 claims description 6
- 241000881813 Pluralibacter gergoviae Species 0.000 claims description 3
- 241000894006 Bacteria Species 0.000 description 13
- 241000195493 Cryptophyta Species 0.000 description 13
- 230000000243 photosynthetic effect Effects 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 229930002875 chlorophyll Natural products 0.000 description 7
- 235000019804 chlorophyll Nutrition 0.000 description 7
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 238000007789 sealing Methods 0.000 description 7
- 238000009825 accumulation Methods 0.000 description 6
- 210000004027 cell Anatomy 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 239000005864 Sulphur Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 229940072056 alginate Drugs 0.000 description 3
- 235000010443 alginic acid Nutrition 0.000 description 3
- 229920000615 alginic acid Polymers 0.000 description 3
- 238000003795 desorption Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229940045505 klebsiella pneumoniae Drugs 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 238000004820 blood count Methods 0.000 description 2
- 238000003501 co-culture Methods 0.000 description 2
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- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
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- 230000031700 light absorption Effects 0.000 description 2
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- 244000005700 microbiome Species 0.000 description 2
- 238000004321 preservation Methods 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 230000031068 symbiosis, encompassing mutualism through parasitism Effects 0.000 description 2
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- 235000013619 trace mineral Nutrition 0.000 description 2
- FRXSZNDVFUDTIR-UHFFFAOYSA-N 6-methoxy-1,2,3,4-tetrahydroquinoline Chemical compound N1CCCC2=CC(OC)=CC=C21 FRXSZNDVFUDTIR-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000195597 Chlamydomonas reinhardtii Species 0.000 description 1
- 241000237505 Chlamys Species 0.000 description 1
- 102000018997 Growth Hormone Human genes 0.000 description 1
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- 108010020056 Hydrogenase Proteins 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- ATPYWZKDGYKXIM-UHFFFAOYSA-N acetic acid phosphoric acid Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.OP(O)(O)=O ATPYWZKDGYKXIM-UHFFFAOYSA-N 0.000 description 1
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- UZKQTCBAMSWPJD-UQCOIBPSSA-N trans-Zeatin Natural products OCC(/C)=C\CNC1=NC=NC2=C1N=CN2 UZKQTCBAMSWPJD-UQCOIBPSSA-N 0.000 description 1
- UZKQTCBAMSWPJD-FARCUNLSSA-N trans-zeatin Chemical compound OCC(/C)=C/CNC1=NC=NC2=C1N=CN2 UZKQTCBAMSWPJD-FARCUNLSSA-N 0.000 description 1
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- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
A process for increasing the hydrogen releasing efficiency of chlamydomonas features use of the dominant complementation between phycobionts.
Description
Technical field
The present invention relates to the biological hydrogen production field, more specifically, the present invention relates to a kind of method that improves hydrogen releasing efficient of chlamydomonas.
Background technology
Miniature green alga breeding is fast, it is wide to distribute, easily culture, automatically tissue collecting's luminous energy, spontaneous accumulation energy and directed conversion fast, therefore green alga hydrogen manufacturing is technology most economical from now on, convenient, that easily realize, but the assessment report of international energy office in 1998 thinks that the photodissociation silicol process of green alga traitor's property hydrogen enzyme is the research direction that application prospect is arranged most.States such as the U.S., Germany, Japan all drop into the hydrogen manufacturing of huge fund biological support, in the hope of entering industrialization production as early as possible, the bottleneck of energy restriction and environmental pollution in the breakthrough process of economic development.
[1] [2] [3] [4](reference of this paper is represented with Arabic numerals, see hereinafter with reference document part for details) Melis of Univ California-Berkeley professor finds that breakthroughly the shortage of element sulphur reversibly, optionally suppresses the chlamydomonas photosynthetic oxygen evolution, but to the but almost not influence of mitochondrial respiratory speed, the imbalance between the so photosynthetic and respiratory rate has just caused O in the sealing algae liquid
2Clean consumption, finally reach the anaerobic state that can induce hydrogenase gene to express.This method has been avoided the susceptibility of iron hydrogen enzyme to oxygen, in time photosynthetic oxygen evolution, the photosynthetic hydrogen of putting has been separated, and has another name called " the photosynthetic hydrogen method of putting of two steps ".
[5]This is the present state-of-the-art hydrogen methods of putting that promotion prospect is arranged most, charges into the rare gas element deoxygenation than the usefulness that has continued 60 years and puts the traditional method of hydrogen and be a a progressive step, and has increased substantially hydrogen releasing efficient.But because some still unsharp limiting factors, the hydrogen releasing efficient of this method is low, put hydrogen and just remain on the baseline values of putting oxygen, must add sulphur at a lack of sulfur after 100 hours, its hydrogen releasing efficient has only 15% of frustule photosynthetic capacity, 15% of just normal photosynthetic oxygen evolution ability, hydrogen 5-7 milliliter is put in every milligram of chlorophyll accumulation
[5], how further to improve with the chlamydomonas is the photosynthetic hydrogen releasing efficient of the miniature green alga of representative, makes it to move towards industrialization, has just become the focus of present research
[1] [3] [4]
The photosynthetic hydrogen of putting of present miniature green alga still is in the exploratory stage, and for improving hydrogen releasing efficient, scientists is being walked two paths.Article one, be to be conceived to improve hydrogen releasing efficient, cultivate such as the chlamydomonas synchronization with the way of Physiology and biochemistry, the content of acetate in the chlamydomonas substratum, the methods such as adjusting of the pH value of chlamydomonas substratum, these methods increase to hydrogen releasing efficient, but can not be multiplied
[6]Another approach utilizes molecular biological means to attempt to improve hydrogen releasing efficient exactly
[7] [8] [9]Screen aerotolerant chlamydomonas mutant strain, change the binding site of hydrogen enzyme and oxygen, theoretical yield can be multiplied, but, because gene information finite capacity in the single cell, additional alien gene on cell proliferation and metabolism system are undoubtedly a kind of burden, so gene dosage that can import in single cell and size are limited; And when utilizing the cell of gene recombination, another bottleneck problem that runs into is that the host cell kind that can utilize is very limited, because product does not only rest in the cell and do not have activity under many situations, this brings very big trouble for follow-up sepn process, and is unstable behind the subculture.
Melis two step puts run out oxygen in the solution of respiration that the hydrogen method relies on chlamydomonas fully, time is longer relatively, the growth conditions of chlamydomonas further is affected, the electronics that photosynthetic hydrolysis generates also remains seldom, influenced hydrogen discharging rate, chlamydomonas is also consuming glacial acetic acid after sealing is cultivated simultaneously, and medium pH value constantly rises, the proton that solution can provide reduces relatively, has also influenced hydrogen discharging rate.Chlamydomonas is under the stress conditions that lacks element sulphur and sealing cultivation in addition, and growth conditions obviously descends, and influences whole ability performance of putting hydrogen.
Summary of the invention
At above-mentioned research background, inventor further investigation, filter out can with the symbiotic facultative aerobe of chlamydomonas, utilize the mutual supplement with each other's advantages of helotisn, improved two steps of Melis to put the hydrogen releasing efficient of hydrogen method.Principle of the present invention is: at first, in initial enclosed environment, facultative aerobe in the algae-bacteria symbiotic system can consume rapidly still and carry out the oxygen that normal photosynthetic chlamydomonas is emitted, and helps to reach in 24-30 hour in advance the solution anaerobic state, promotes the hydrogen enzymic synthesis to put hydrogen; Secondly, after solution was anaerobic state, this bacterium can secrete H
+In solution, put hydrogen for algae sufficient proton source is provided, further improve hydrogen generation efficiency.In addition, bacterium can secrete some active substances in process of growth, and such as growth hormone, zeatin etc. promote and the better existence under the adverse circumstance state of help chlamydomonas that growth conditions is better, thereby improves the Hydrogen Energy power of putting of chlamydomonas.
Therefore, an object of the present invention is to provide the method that two steps of a kind of Melis of raising put the hydrogen releasing efficient of chlamydomonas of hydrogen method, it is characterized in that chlamydomonas is tieed up enterobacteria (Enterobacter gergoviae) with colluding facultative aerobe day
[10]Or Klebsiella pneumonia (Klebsiellapneumoniae) or acid-producing Klebsiella bacterium (Klebsiella oxytoca) cultivation altogether.In one embodiment, colluding the dimension enterobacteria day is to collude dimension enterobacteria 57-7 (CGMCC No.0510 day, it has been announced in China Patent No. ZL00133626.6 (first contriver Lee Yongxing) and has authorized, be deposited in China Committee for Culture Collection of Microorganisms common micro-organisms center), Klebsiella pneumonia (Klebsiella pneumoniae) AS 1.1734 and acid-producing Klebsiella bacterium (Klebsiellaoxytoca) AS 1.1878 are available from China Committee for Culture Collection of Microorganisms common micro-organisms center, and chlamydomonas is Chlamy reinhardtii cc125mt+ (U.S. Duke university chlamydomonas center provides).
In one embodiment of the invention, the cultivation respectively earlier of dimension enterobacteria, Klebsiella pneumonia, acid-producing Klebsiella bacterium will be colluded chlamydomonas and day, cultivation altogether again when waiting to put hydrogen.
In another embodiment of the invention, wherein chlamydomonas is and colludes immobilized day dimension enterobacteria, Klebsiella pneumonia, acid-producing Klebsiella bacterium and cultivate altogether.
To collude the dimension enterobacteria day is that the hydrogen releasing efficient of two steps that experiment showed, Melis of example putting the hydrogen method is every liter of algae liquid (3-6 * 10
6Individual/ml), hydrogen 5-7 milliliter is put in every milligram of chlorophyll accumulation, and compound phycomycete co-culture system of the present invention by contrast can improve 1.5 times with unit algae liquid hydrogen releasing efficient, and hydrogen 7.5-11.8 milliliter is put in every milligram of chlorophyll accumulation.In addition, two steps of Melis put the hydrogen method a lack of sulfur sealing after 48 hours chlamydomonas just can begin to put hydrogen, and utilize method of the present invention between 12-24 hour, just can put hydrogen, put the hydrogen time and shifted to an earlier date 24-36 hour.Therefore, method of the present invention has significantly improved Melis two step and has put the hydrogen releasing efficient of chlamydomonas of hydrogen method, the mass-producing of putting hydrogen for little algae use provide a kind of new may.
Description of drawings
The present invention is described in further detail below in conjunction with the drawings and specific embodiments, is that the present invention is limited but should not be construed as.
Fig. 1. simple two steps of Melis put the hydrogen method and the comparison of the hydrogen releasing efficient of hydrogen method is put in phycomycete (colluding the dimension enterobacteria day) symbiosis;
Fig. 2. simple two steps of Melis put the comparison that hydrogen method and immobilized bacterium (colluding the dimension enterobacteria day) and algae symbiosis are put the hydrogen releasing efficient of hydrogen method.
Embodiment
Below to collude the dimension enterobacteria day for exemplifying example explanation embodiment of the present invention.
Embodiment 1 helotisn is put the hydrogen method
1. experiment material and instrument: chlamydomonas Chiamy reinhardtii cc125mt+, wild-type is buied from Duke Univ USA chlamydomonas center.
Cultural method: Tris-acetate-phosphate substratum (TAP)
[11]
NH
4Cl 0.4g/L
MgSO
4·7H
2O 0.1g/L
CaCl
2 0.0377g/L
K
2HPO
4 0.108g/L，
KH
2PO
4 0.056g/L
Tris 2.42g/L
Glacial acetic acid 1ml
Trace element 1ml
The substratum of TAP-S then is containing SO
4 2-Salt all use corresponding C l
-Salt replace, comprise the vitriol in the trace element.
ST-04 minor amount of water chromatographic instrument (Beijing Analytical Instrument Factory), thermal conductivity detector, N
2As carrier gas, external standard method, chromatographic working station JF-9902 (Beijing Analytical Instrument Factory)
HITACHI 20PR-520 whizzer
Oxygen electrode (Hansatech)
8500II spectrophotometer ultraviolet spectrophotometer (Shanghai Techcomp Instrument Ltd.)
XB-K-25 type blood cell counting plate (Zhejiang Province's Yuhuan county's refinement medical apparatus factory)
2. experimental technique and result
Chlorophyll measuring method:
[12]
Get 1ml algae liquid to be measured, add 5ml 80% acetone, the vibration mixing left standstill 1 hour in 4 ℃, and centrifugal 5 minutes of 5000g behind the mixing gets supernatant again, measures 663nm, the absorption value at 645nm place,
Chlorophyll(a+b)mg/ml＝(20.2×A645+8.02×A663)×5
The inoculation that falls of the single algae of chlamydomonas is placed in the triangular flask that contains the TAP substratum 100 μ mol/m
2The continuous light of/s, 25 ℃, nonoscillatory, the CO of logical 3-5%
2, cultivated in the above conditions 6 to 7 days, reach 3-6 * 10
6Individual/as during ml concentration (counting with blood cell counting plate), to add at 1: 10 with volume ratio in the substratum of TAP-S, continued growth is when reaching 2-5 * 10
6Individual/during ml concentration, sealing is cultivated, add simultaneously to collude dimension enterobacteria (Enterobactergergoviae) 57-7 the day of cultivating 15 hours
[7]It is identical with the TAP-S of C.reinhardtii to collude the used substratum of dimension enterobacteria 57-7 day, and the nutrient solution volume is 1/2 of an algae liquid, and the light absorption value OD at 600nm place is between the 0.4500-0.6000, adds stirrer, and the sealing continuous illumination is cultivated.Method according to reported in literature is measured hydrogen desorption capacity with draining water gathering of gas law, uses the gas chromatographic measurement hydrogen purity
[5]The chlamydomonas of colluding the dimension enterobacteria day with not adding under the same culture conditions is measured hydrogen desorption capacity in contrast.Experimental result is seen Fig. 1, and data are the mean value of 6 experiments.Two steps of Melis put hydrogen method chlamydomonas after a lack of sulfur seals 48 hours and just can begin to put hydrogen, and hydrogen releasing efficient is every liter of algae liquid (3-6 * 10
6Individual/ml), hydrogen 5-7 milliliter is put in every milligram of chlorophyll accumulation, and phycomycete co-culture system of the present invention promptly began to have the hydrogen output after 12 hours, reached the climax in 48 hours to 72 hours, can put continuously hydrogen 120-140 hour, unit algae liquid hydrogen releasing efficient on average improves 1.5 times, and hydrogen 7.5-11.8 milliliter is put in every milligram of chlorophyll accumulation.
The common cultivation of embodiment 2 chlamydomonas and immobilized bacterium
1. experimental drug
4% sodiun alginate, the 4 ℃ of preservations of sterilizing, 0.05mol/L CaCl
2
2. bacteria immobilization method
1) the centrifugal receipts thalline of .1000g, aseptic washing twice, used bacterium liquid OD
600Between 0.5000-0.6000;
2). the gained bacterium is stuck with paste the TAP-S substratum mixing that adds 1/3 volume;
3). add 4% sodiun alginate of 2 times of volumes, fully mixing;
4). with 0.05mol/l CaCl
2In 37 ℃ of water bath heat preservations 10 minutes;
5). the mixed solution that sodiun alginate and bacterium are stuck with paste is packed in the syringe, at the uniform velocity divides with No. 9 syringe needles to splash into CaCl
2In the solution;
6). the solution that inclines, with aseptic deionized water flushing 1 time;
7). add 00.05mol/L CaCl again
2Solution was in 4 ℃ of balances 6 hours;
8). CaCl inclines
2Solution, stand-by after usefulness TAP-S substratum cleans 2 times with the gauze parcel.
As culture condition and cultural method as described in the embodiment 1, cultivate chlamydomonas and day respectively and collude the dimension enterobacteria.With the light absorption value OD at 600nm place of results is that colluding day between the 0.4500-0.6000 tieed up enterobacteria and be fixed into the bacterium pearl by above bacteria immobilization method.To cultivate 3-6 * 10
6The centrifugal results of chlamydomonas 1000g of individual/ml concentration are inserted among the TAP-S after cleaning twice with TAP-S (not containing element sulphur) substratum, and the bacterium pearl pouch of simultaneously said fixing being handled well hangs and is immersed in algae liquid central authorities, continues the sealing irradiation and cultivates.With the simple chlamydomonas under the same culture conditions in contrast, experimental result is seen Fig. 2, and data are the mean value of 6 experiments.Compare with simple Melis method, the hydrogen time that puts of immobilized bacterium and algae syntaxial system is not obvious in advance, but hydrogen desorption capacity still increases, and so the sustainable use of bacterium pearl three months effectively.Hydrogen releasing efficient is constant.
In another embodiment of the invention, the chlamydomonas material is constant, colludes the dimension enterobacteria day and becomes Klebsiella pneumonia or acid-producing Klebsiella bacterium, and all the other experimental procedures are all identical, draw similar experimental result, not accompanying drawing in addition.
Experiment showed, that the laboratory common vinelandii Klebsiella pneumonia of other two strains (Klebsiella pneumoniae) AS 1.1734 and acid-producing Klebsiella bacterium (Klebsiellaoxytoca) AS 1.1878 commonly used also have effect same.
Should be appreciated that those skilled in the art can make various changes or modifications the present invention after having read above-mentioned teachings of the present invention, but the equivalent form of value of changing or revising drops on equally in the application's claims institute restricted portion.
Reference
[1] Thomas Happe and Anja Hemschemeier (2002) Hydrogenases ingreen algae:do they save the algae ' s life and solve our energyproblems? Trends in Plant Science, Vol.7 No.6
[2]McKendry，P.(2002)Energy?production?from?biomass(Part1)：Overview?of?biomass.Bioresour?Technol，83，37-46
[3] Melis, A. and Happe, T. (2001) Hydrogen production.Greenalgae as a source of energy.Plan t Physiol, 127,740-748
[4]Melis?A(2002)Green?alga?hydrogen?production：progress，challenges?and?prospects.Intl.J.Hydrogen?Energy?27：1217-1228
[5] Melis A, Zhang L., Forestier M., Ghirardi M.L. and SeibertM. (2000) .Sustained Photobiological Hydrogen Gas Production uponReversible Inactivation of Oxygen Evolution in the Green AlgaChlamydomonas reinhardtii.Plant Physiol.122 (1): 127-136
[6] Sergey Kosourov and Anatoly Tsygankov (2002) SustainedHydrogen Photoproduction by Chlamydomonas reinhardtii:Effects ofCulture parameters, Biotechnology and Bioengineering, Vol.78, NO.7
[7] Happe, T. and Kaminski, A. (2002) Differential regulationof the Fe-hydrogenase during anaerobic adaptation in the green algaChlamydomonas reinhardtii.Eur J Biochem, 269,1022-1032
[8] Happe, T., Mosler, B. and Naber, J.D. (1994) Induction, localization and metal content of hydrogenase in the green algaChlamydomonas reinhardtii.Eur J Biochem, 222,769-774
[9] Winkler, M., Hemschemeier, A., Gotor, C., Melis, A. and Happe, T. (2002b) Fe-hydrogenases in green algae:photo-fermentation andhydrogen evolution under sulfur deprivation.Internattional Journalof Hydrogen Energy, 27,1431-1439
[10] Li Yongxing etc., " colluding the characteristic research of dimension enterobacteria Enterobactergergoviae 57-7 corn rhizosphere combination azotobacter day " microorganism journal 1993,6:454-458
[11]Elizabeth?H.Harris(1989)The?Chlamydomonas?Sourcebook，Academic?Press，Inc
[12]Arnon，D.I.(1949)Copper?enzymes?in?isolated?choroplasts.Polyphenoloxidase?in?Beta?vulgaris.Plant?physiol.24，1-15
Claims (8)
1. one kind is improved the method that two steps of Melis put the hydrogen releasing efficient of chlamydomonas of hydrogen method, it is characterized in that chlamydomonas and facultative anaerobe are cultivated altogether.
2. according to the process of claim 1 wherein that described facultative anaerobe is to collude dimension enterobacteria (Enterobacter gergoviae), Klebsiella pneumonia (Klebsiella pneumoniae) or acid-producing Klebsiella bacterium (Klebsiella oxytoca) day.
3. according to the method for claim 2, colluding the dimension enterobacteria wherein said day is to collude dimension enterobacteria CGMCC No.0510 day.
4. according to the method for claim 2, wherein said Klebsiella pneumonia is Klebsiella pneumonia (Klebsiella pneumoniae) AS 1.1734.
5. according to the method for claim 2, wherein said acid-producing Klebsiella bacterium (Klebsiellaoxytoca) is acid-producing Klebsiella bacterium (Klebsiella oxytoca) AS 1.1878.
6. according to any one method among the claim 1-5, wherein said chlamydomonas is Chlamyreinhardtii cc125mt+.
7. according to any one method among the claim 1-5,, cultivate altogether again when waiting to put hydrogen wherein with chlamydomonas with collude dimension enterobacteria, Klebsiella pneumonia, acid-producing Klebsiella bacterium day and cultivate respectively earlier.
8. according to any one method among the claim 1-5, wherein chlamydomonas is and colludes dimension enterobacteria, Klebsiella pneumonia, acid-producing Klebsiella bacterium immobilized day and cultivate altogether.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200510011297 CN1280405C (en) | 2005-02-03 | 2005-02-03 | Method of increasing hydrogen releasing efficient of chlamydomonas |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101367575B (en) * | 2008-10-06 | 2010-04-14 | 首都师范大学 | Method for resourceful treatment of cadmium polluted wastewater |
| CN107254413A (en) * | 2017-08-16 | 2017-10-17 | 扬州大学 | A kind of method by being co-cultured with immobilized microorganism using starch Heterotrophic culture microalgae |
| CN107287123A (en) * | 2017-07-27 | 2017-10-24 | 扬州大学 | A kind of method co-cultured by immobilized microorganism using sucrose Heterotrophic culture microalgae |
| CN107119103B (en) * | 2017-06-29 | 2019-02-26 | 哈尔滨工业大学 | A kind of anaerobic hydrogen-generating bacterium and aerobic bacteria breathe the aerobic production hydrogen methods of interaction |
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2005
- 2005-02-03 CN CN 200510011297 patent/CN1280405C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101367575B (en) * | 2008-10-06 | 2010-04-14 | 首都师范大学 | Method for resourceful treatment of cadmium polluted wastewater |
| CN107119103B (en) * | 2017-06-29 | 2019-02-26 | 哈尔滨工业大学 | A kind of anaerobic hydrogen-generating bacterium and aerobic bacteria breathe the aerobic production hydrogen methods of interaction |
| CN107287123A (en) * | 2017-07-27 | 2017-10-24 | 扬州大学 | A kind of method co-cultured by immobilized microorganism using sucrose Heterotrophic culture microalgae |
| CN107254413A (en) * | 2017-08-16 | 2017-10-17 | 扬州大学 | A kind of method by being co-cultured with immobilized microorganism using starch Heterotrophic culture microalgae |
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| CN1280405C (en) | 2006-10-18 |
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