微生物细胞CO_2跨膜转运的研究进展

CO_2是自然界储量巨大的游离性碳资源。关于CO_2的生物转化,除了我们所熟知的植物光合作用外,许多微生物亦具备此能力。微生物利用CO_2的首要步骤是完成CO_2从细胞外向细胞内的跨膜转运,这也是决定微生物CO_2利用效率的重要环节。本文中,笔者对目前微生物CO_2跨膜转运的研究进展进行了总结,重点阐述了各类微生物CO_2运输元件及其工作的分子机制以及通过优化CO_2转运提高微生物利用CO_2能力的策略。在此基础上,笔者还提出了今后微生物转化利用CO_2的研究重点和关键科学问题,可为未来通过生物路线实现CO_2的资源化利用提供借鉴。     

吸入不同浓度 CO_2对肺通气功能影响的实验观察

本实验在10名健康男性青年中观察了吸入0.5—7%CO_2对肺通气功能的影响。实验结果表明,呼吸频率、潮气量、肺通气量、肺泡 CO_2分压以及肺通气对 CO_2的反应性均与吸入气CO_2浓度成线性关系。被试者吸入 CO_2后,CO_2排出量减少;但浓度不超过5%时,3—5min 内CO_2排出量即可基本恢复到正常水平。本文根据人体 CO_2反应的这些特点提出了三个代偿区的意见。     

代谢工程改造异养微生物固定CO2研究进展

环境保护和能源供应是人类关心的两大问题。能源消耗释放出的温室气体对环境造成了严重影响。利用CO_2固定途径可将CO_2转化成燃料或化学品。天然固碳生物通常存在生长缓慢、固碳效率低等问题。通过在模式微生物中增强或重构CO_2固定途径,实现CO_2的再循环,可提高燃料或化学品的产量,减少温室气体排放。文中详细介绍了通过代谢工程手段改造CO_2固定途径改善化学品生产以及糖合成,阐述了相关代谢途径及其中的关键酶在CO_2固定中的作用,介绍了电生化合成系统的应用,显示出CO_2固定的巨大潜力,并展望了未来CO_2固定的研究方向。     

大豆主要株型和产量指标对大气CO2和温度升高的响应

针对当前气候变暖和大气CO_2浓度升高同步发生现实,以高光效大豆品种黑农41(HN41)和3个常规对照品种周豆16号(ZD16)、中豆35号(ZD35)和桂黄豆2号(GHD2)为研究对象,通过开顶式气室模拟高CO_2浓度(650μL/L)和温度升高(±0.5—0.6℃)研究了大气CO_2和温度升高对大豆的生长发育与产量影响。结果表明,CO_2浓度升高对株高、茎粗、单株干重和单株籽粒重影响极显著;温度、CO_2与品种互作极显著地影响单株籽粒重。CO_2浓度升高有增加大豆株高、茎粗、干重和单株籽粒重的趋势,且高温下CO_2浓度升高对株高和茎粗的促进作用更大,而正常温度水平下高CO_2浓度升高更有利于干物质积累。与对照CO_2浓度比,高CO_2浓度显著促进了高温下HN41、ZD16和GHD2的株高,并显著提高了正常温度下HN41、ZD16、ZD35和GHD2的单株干重。与正常温度相比,高温仅显著提高了高CO_2处理下HN41的茎粗,并显著提高了对照CO_2处理下HN41的单株籽粒重。此外,同一CO_2浓度和温度处理下,高光效大豆HN41的茎粗、根冠比和单株籽粒重等都显著高于ZD16、ZD35和GHD2;而仅在正常温度与高CO_2浓度处理下HN41的单株干重显著高于ZD16和GHD2。CO_2浓度和温度升高显著影响了高光效大豆的生长,其中,高温下CO_2浓度升高有利于其生长势,正常温度下CO_2浓度升高有利于其光合产物积累。     

增施二氧化碳生理效应的初步研究

空气中CO_2的浓度往往是限制植物光合作用的重要因素。因此,增施CO_2就成为促进作物增产的有效措施。近年来,各种覆盖栽培在蔬菜生产中的应用,既造成了保护地内CO_2的局部亏缺,也使增施的CO_2不易逸散。这对田间应用增施CO_2的措施既提出了要求,又创造了条件。1975年以来,我们在北京郊区进行了一些增施CO_2的试验。我们初步观察到,叶菜类的增产     

改变肺通气量对猫脑干中缝大核区神经元放电的影响

本工作通过改变人工呼吸的通气量使肺泡气的CO_2浓度发生变化,观察其对猫脑干中缝大核区神经细胞自发放电的影响。发现每个神经细胞都有自己稳定放电的肺泡气CO_2浓度范围。有些神经细胞,这个浓度范围很小,对肺泡气CO_2浓度的改变非常敏感,而有少数神经细胞对肺泡气CO_2浓度的改变则很不敏感。当肺泡气CO_2浓度越出稳定放电的肺泡气CO_2浓度范围后,神经细胞的放电就会减少,或者增加。根据反应的不同,可将细胞分为三类:第一类细胞,当肺泡气CO_2浓度小于稳定放电的CO_2浓度范围时,放电减少;而当大于稳定放电的CO_2浓度范围时,放电增多。第二类细胞,当肺泡气CO_2浓度小于稳定放电的CO_2浓度范围时,放电增多;而当大于稳定放电的CO_2浓度范围时,放电减少。第三类细胞,当肺泡气CO_2浓度小于或大于稳定放电的CO_2浓度范围时,放电均减少。     

腐食酪螨对低氧高二氧化碳气调的抗性

在10％CO_2,5％O_2(其余部分为N_2,下同);35％CO_2,11％CO_2;35％CO_2,21％O_2;75％CO_2,11％O_2,及75％CO_2,21％O_2,五种气调环境下对腐食酪螨Tyrophagus putrescentiae(Schrank)进行连续25～26代的抗气性诱导筛选。结果表明,抗性都有不同程度的增加,在75％CO_2,11％O_2下抗性系数最大为5.0,在10％CO_2,5％O_2下抗性系数最小为3.7,在其它气调环境下,抗性系数都在4以上。     

高CO2浓度对杂交水稻光合作用日变化的影响——FACE研究

大气二氧化碳(CO_2)浓度增高导致全球变暖,但作为光合作用底物促进绿色作物的光合作用。为了明确高CO_2浓度对杂交水稻结实期光合日变化的影响,2014年利用稻田FACE(Free Air CO_2Enrichment)平台,以生产上曾创高产纪录的两个杂交稻新组合甬优2640和Y两优2号为供试材料,设置环境CO_2和高CO_2浓度(增200μmol/mol)两个水平,测定杂交稻抽穗期和灌浆中期光合作用日变化和成熟期生物量。结果表明,高CO_2浓度环境下两组合抽穗期叶片净光合速率均大幅增加(全天平均52%),但灌浆中期的平均增幅减半,其中Y两优2号这种光合下调表现更为明显。大气CO_2浓度升高使两杂交稻组合抽穗和灌浆中期叶片气孔导度均大幅下降,导致蒸腾速率下降而水分利用效率大幅增加,Y两优2号气孔导度和蒸腾速率对CO_2的响应上午大于下午,而甬优2640表现相反。尽管大气CO_2浓度升高使杂交稻结实期不同时刻胞间CO_2浓度均大幅增加,但对气孔限制值特别是胞间CO_2与空气CO_2浓度之比多无显著影响,两品种趋势一致。大气CO_2浓度升高对甬优2640地上部生物量及其组分的影响明显大于Y两优2号,CO_2与品种间多存在互作效应。以上结果表明,与甬优2640相比,Y两优2号最终生产力从高CO_2浓度环境中获益较少可能与该品种生长后期存在明显的光合适应有关,但这种光合适应似乎不是由气孔限制造成的。     

一种简易实用的CO2培养装置

近年来由于杂交瘤技术和细胞培养方法的发展,CO_2培养箱的使用日益广泛。目前进口或国产的CO_2培养箱价格昂贵,货源较缺,并需配CO_2钢瓶,因此某些地区的一般实验室购置和使用常有困难。有人采用烛罐法或通过范氏气体定量器通CO_2至厌氧罐法作为替代,但有CO_2量不易控制或操作较繁复之弊。本文介绍我们试制的一种用化学法产生CO_2的简易CO_2培养装置。     

皆伐火烧对亚热带森林不同深度土壤CO2通量的影响

评估不同深度土壤的CO_2通量是研究土壤碳动态的重要手段。目前有关皆伐火烧对森林土壤碳排放的影响研究仅局限于表层土壤,而对不同深度土壤碳排放影响鲜见报道。以米槠(Castanopsis carlesii)次生林(对照)及其皆伐火烧后林地为研究对象,利用非红外散射CO_2探头测定土壤CO_2浓度,并结合Fick第一扩散法则估算不同深度(0—80 cm)土壤CO_2通量。结果表明:(1)皆伐火烧改变土壤向大气排放的表观CO_2通量,在皆伐火烧后的2个月内土壤表观CO_2通量显著高于对照68%;2个月后,土壤表观CO_2通量低于对照37%。(2)皆伐火烧后,除10—20 cm的CO_2通量提高外,其余各深度(0—10、20—40、40—60 cm和60—80 cm)的CO_2通量均降低。同时,皆伐火烧改变不同土层对土壤呼吸的贡献率,降低0—10 cm土层的贡献率,提高10—20 cm土层的贡献率。(3)对照样地仅0—10 cm土壤CO_2通量与温度呈显著指数相关,10—40 cm深度CO_2通量则与土壤含水率呈显著线性相关。皆伐火烧后0—10 cm和10—20 cm处土壤的CO_2通量均与温度呈指数相关。说明皆伐火烧改变了不同深度土壤CO_2通量对于环境因子的响应。因此为准确评估和预测皆伐火烧对土壤与大气间碳交换的影响,应考虑皆伐火烧后不同时期土壤CO_2通量的变化,以及不同深度土壤CO_2通量对皆伐火烧的响应。     

The CO2-SFE crude lipid extract and the free fatty acid extract from Perna canaliculus have anti-inflammatory effects on adjuvant-induced arthritis in rats

The anti-inflammatory (AI) activity of a supercritical fluid extract (CO(2)-SFE) of tartaric acid-stabilised Perna canaliculus mussel powder, and of the free fatty acid (FFA) class separated from the CO(2)-SFE extract by column chromatography, was investigated in the rat adjuvant arthritis model. Administration of the CO(2)-SFE extract (100 mg/kg BW/day s.c.) for 15 days post-adjuvant inoculation significantly reduced rear paw swelling by 34% and the deterioration in total body condition by 52% in arthritic rats, compared to vehicle controls. These observations were accompanied by a decreased serum ceruloplasmin oxidase activity, and reduced inflammatory response of the spleen. The mussel FFA extract given at one third of the dose (30 mg/kg BW/day s.c.) and for a shorter treatment period (5 days during the inflammatory phase) achieved an even greater AI activity, and was equipotent to piroxicam (2 mg/kg BW/day s.c.). Preliminary toxicology assessment using both arthritic and non-arthritic (healthy) rats revealed no significant differences between the mussel treatment groups and respective vehicle controls in either organ weights, tissue histology or selected biochemical parameters. These results indicate the CO(2)-SFE crude lipid extract and its FFA components from stabilised P. canaliculus mussel powder contain biologically significant AI activity in vivo, with no apparent adverse side effects.     

灵芝孢子油脂肪酸组分的分析

采用气相色谱与质谱(GC-MS)联用分析,从超临界CO2萃取孢子油中鉴定出18种脂肪酸成分,包括6种不饱和脂肪酸、7种饱和脂肪酸、2种环链脂肪酸,以及己酸、辛酸、壬酸等短链脂肪酸。GC定量分析结果表明:灵芝孢子油中检出9种已知脂肪酸,不饱和脂肪酸总量为73.6%;其中,主体成分油酸(C18∶1)、亚油酸(C18∶2)和棕榈酸(C16∶0)等含量分别为57.5%、13.4%、19.6%;此外,不饱和脂肪酸十六碳烯酸(C16∶1)、亚麻酸(C18∶3)等不饱和脂肪酸含量为2.2%、0.5%。     

Effects of hyper- and hypoventilation on gastric and sublingual PCO(2).

We investigated the effects of hyper- and hypoventilation on gastric (Pg(CO(2))) and sublingual (Psl(CO(2))) tissue PCO(2) before, during, and after reversal of hemorrhagic shock. Pg(CO(2)) was measured with ion-sensitive field-effect transistor sensor and Psl(CO(2)) with a CO(2) microelectrode. Under physiological conditions and during hemorrhagic shock, decreases in arterial (Pa(CO(2))) and end-tidal (PET(CO(2))) PCO(2) induced by hyperventilation produced corresponding decreases in Pg(CO(2)) and Psl(CO(2)). Hypoventilation produced corresponding increases in Pa(CO(2)), PET(CO(2)), Pg(CO(2)), and Psl(CO(2)). Accordingly, acute decreases and increases in Pa(CO(2)) and PET(CO(2)) produced statistically similar decreases and increases in Pg(CO(2)) and Psl(CO(2)). No significant changes in the tissue PCO(2)-Pa(CO(2)) gradients were observed during hemorrhagic shock in the absence or in the presence of hyper- or hypoventilation. Acute changes in Pg(CO(2)) and Psl(CO(2)) should, therefore, be interpreted in relationship with concurrent changes in Pa(CO(2)) and/or PET(CO(2)).     

Temperature, oxygen, and salt-sensing neurons in C. elegans are carbon dioxide sensors that control avoidance behavior

Homeostatic control of body fluid CO(2) is essential in animals but is poorly understood. C.?elegans relies on diffusion for gas exchange and avoids environments with elevated CO(2). We show that C.?elegans temperature, O(2), and salt-sensing neurons are also CO(2) sensors mediating CO(2) avoidance. AFD thermosensors respond to increasing CO(2) by a fall and then rise in Ca(2+) and show a Ca(2+) spike when CO(2) decreases. BAG O(2) sensors and ASE salt sensors are both activated by CO(2) and remain tonically active while high CO(2) persists. CO(2)-evoked Ca(2+) responses in AFD and BAG neurons require cGMP-gated ion channels. Atypical soluble guanylate cyclases mediating O(2) responses also contribute to BAG CO(2) responses. AFD and BAG neurons together stimulate turning when CO(2) rises and inhibit turning when CO(2) falls. Our results show that C.?elegans senses CO(2) using functionally diverse sensory neurons acting homeostatically to minimize exposure to elevated CO(2).     

Topical inhibition of nasal carbonic anhydrase affects the CO2 detection threshold in rats

Previous studies indicate that Long-Evans rats can be operantly trained to discriminate inspired CO(2) concentrations as low as 0.5%. This ability has been proposed to be due to the presence of CO(2)-sensitive olfactory receptors that contain the enzyme carbonic anhydrase (CA). The objectives of the present study were as follows: 1) to determine whether Zucker rats could be operantly conditioned to discriminate low concentrations of CO(2) from control air and 2) to determine the rats' CO(2) detection thresholds before and after nasal perfusion of mammalian Ringers or methazolamide, a CA inhibitor. Rats were operantly trained to discriminate between 25% CO(2) and control air (0% CO(2)) and were then subjected to various CO(2) concentrations (0.5-12.5%) to determine their CO(2) detection thresholds. The average (+/-standard error of mean) baseline CO(2) detection threshold of 7 Zucker rats was 0.48 +/- 0.07% CO(2), whereas the average CO(2) detection thresholds after nasal perfusion of either mammalian Ringers or 10(-2) M methazolamide were 1.41 +/- 0.30% and 5.92 +/- 0.70% CO(2), respectively. The average CO(2) detection threshold after methazolamide was significantly greater (P<0.0001) than the baseline detection threshold. These findings demonstrate that like Long-Evans rats, Zucker rats can be trained to discriminate low concentrations of CO(2) and that inhibition of nasal CA reduces the ability of the rats to detect low concentrations (3.5% and below) but not higher concentrations of CO(2) (12.5%). These results add to the growing evidence that olfactory neurons exhibiting CA activity are CO(2) chemoreceptors sensitive to physiological concentrations of CO(2).     

The effect of CO2 availability on the growth, iron oxidation and CO2-fixation rates of pure cultures of Leptospirillum ferriphilum and Acidithiobacillus ferrooxidans

Understanding how bioleaching systems respond to the availability of CO(2) is essential to developing operating conditions that select for optimum microbial performance. Therefore, the effect of inlet gas and associated dissolved CO(2) concentration on the growth, iron oxidation and CO(2) -fixation rates of pure cultures of Acidithiobacillus ferrooxidans and Leptospirillum ferriphilum was investigated in a batch stirred tank system. The minimum inlet CO(2) concentrations required to promote the growth of At. ferrooxidans and L. ferriphilum were 25 and 70 ppm, respectively, and corresponded to dissolved CO(2) concentrations of 0.71 and 1.57 μM (at 30°C and 37°C, respectively). An actively growing culture of L. ferriphilum was able to maintain growth at inlet CO(2) concentrations less than 30 ppm (0.31-0.45 μM in solution). The highest total new cell production and maximum specific growth rates from the stationary phase inocula were observed with CO(2) inlet concentrations less than that of air. In contrast, the amount of CO(2) fixed per new cell produced increased with increasing inlet CO(2) concentrations above 100 ppm. Where inlet gas CO(2) concentrations were increased above that of air the additional CO(2) was consumed by the organisms but did not lead to increased cell production or significantly increase performance in terms of iron oxidation. It is proposed that At. ferrooxidans has two CO(2) uptake mechanisms, a high affinity system operating at low available CO(2) concentrations, which is subject to substrate inhibition and a low affinity system operating at higher available CO(2) concentrations. L. ferriphilum has a single uptake system characterised by a moderate CO(2) affinity. At. ferrooxidans performed better than L. ferriphilum at lower CO(2) availabilities, and was less affected by CO(2) starvation. Finally, the results demonstrate the limitations of using CO(2) uptake or ferrous iron oxidation data as indirect measures of cell growth and performance across varying physiological conditions.     

Long-term growth of soybean at elevated [CO2] does not cause acclimation of stomatal conductance under fully open-air conditions

Accurately predicting plant function and global biogeochemical cycles later in this century will be complicated if stomatal conductance (g(s)) acclimates to growth at elevated [CO(2)], in the sense of a long-term alteration of the response of g(s) to [CO(2)], humidity (h) and/or photosynthetic rate (A). If so, photosynthetic and stomatal models will require parameterization at each growth [CO(2)] of interest. Photosynthetic acclimation to long-term growth at elevated [CO(2)] occurs frequently. Acclimation of g(s) has rarely been examined, even though stomatal density commonly changes with growth [CO(2)]. Soybean was grown under field conditions at ambient [CO(2)] (378 micromol mol(-1)) and elevated [CO(2)] (552 micromol mol(-1)) using free-air [CO(2)] enrichment (FACE). This study tested for stomatal acclimation by parameterizing and validating the widely used Ball et al. model (1987, Progress in Photosynthesis Research, vol IV, 221-224) with measurements of leaf gas exchange. The dependence of g(s) on A, h and [CO(2)] at the leaf surface was unaltered by long-term growth at elevated [CO(2)]. This suggests that the commonly observed decrease in g(s) under elevated [CO(2)] is due entirely to the direct instantaneous effect of [CO(2)] on g(s) and that there is no longer-term acclimation of g(s) independent of photosynthetic acclimation. The model accurately predicted g(s) for soybean growing under ambient and elevated [CO(2)] in the field. Model parameters under ambient and elevated [CO(2)] were indistinguishable, demonstrating that stomatal function under ambient and elevated [CO(2)] could be modelled without the need for parameterization at each growth [CO(2)].     

End-tidal carbon dioxide tension reflects arterial carbon dioxide tension in the heat-stressed human with and without simulated hemorrhage

End-tidal carbon dioxide tension (Pet(CO(2))) is reduced during an orthostatic challenge, during heat stress, and during a combination of these two conditions. The importance of these changes is dependent on Pet(CO(2)) being an accurate surrogate for arterial carbon dioxide tension (Pa(CO(2))), the latter being the physiologically relevant variable. This study tested the hypothesis that Pet(CO(2)) provides an accurate assessment of Pa(CO(2)) during the aforementioned conditions. Comparisons between these measures were made: 1) after two levels of heat stress (N = 11); 2) during combined heat stress and simulated hemorrhage [via lower-body negative pressure (LBNP), N = 8]; and 3) during an end-tidal clamping protocol to attenuate heat stress-induced reductions in Pet(CO(2)) (N = 7). Pet(CO(2)) and Pa(CO(2)) decreased during heat stress (P < 0.001); however, there was no group difference between Pa(CO(2)) and Pet(CO(2)) (P = 0.36) nor was there a significant interaction between thermal condition and measurement technique (P = 0.06). To verify that this nonsignificant trend for the interaction was not due to a type II error, Pet(CO(2)) and Pa(CO(2)) at three distinct thermal conditions were also compared using paired t-tests, revealing no difference between Pa(CO(2)) and Pet(CO(2)) while normothermic (P = 0.14) and following a 1.0 ± 0.2°C (P = 0.21) and 1.4 ± 0.2°C (P = 0.28) increase in internal temperature. During LBNP while heat stressed, measures of Pet(CO(2)) and Pa(CO(2)) were similar (P = 0.61). Likewise, during the end-tidal carbon dioxide clamping protocol, the increases in Pet(CO(2)) (7.5 ± 2.8 mmHg) and Pa(CO(2)) (6.6 ± 3.4 mmHg) were similar (P = 0.31). These data indicate that mean Pet(CO(2)) reflects mean Pa(CO(2)) during the evaluated conditions.     

12CO2 emission from different metabolic pathways measured in illuminated and darkened C3 and C4 leaves at low,atmospheric and elevated CO2 concentration

The detection of 12CO2 emission from leaves in air containing 13CO2 allows simple and fast determination of the CO2 emitted by different sources, which are separated on the basis of their labelling velocity. This technique was exploited to investigate the controversial effect of CO2 concentration on mitochondrial respiration. The 12CO2 emission was measured in illuminated and darkened leaves of one C4 plant and three C3 plants maintained at low (30-50 ppm), atmospheric (350-400 ppm) and elevated (700-800 ppm) CO2 concentration. In C3 leaves, the 12CO2 emission in the light (Rd) was low at ambient CO2 and was further quenched in elevated CO2, when it was often only 20-30% of the 12CO2 emission in the dark, interpreted as the mitochondrial respiration in the dark (Rn). Rn was also reduced in elevated CO2. At low CO2, Rd was often 70-80% of Rn, and a burst of 12CO2 was observed on darkening leaves of Mentha sativa and Phragmites australis after exposure for 4 min to 13CO2 in the light. The burst was partially removed at low oxygen and was never observed in C4 leaves, suggesting that it may be caused by incomplete labelling of the photorespiratory pool at low CO2. This pool may be low in sclerophyllous leaves, as in Quercus ilex where no burst was observed. Rd was inversely associated with photosynthesis, suggesting that the Rd/Rn ratio reflects the refixation of respiratory CO2 by photosynthesizing leaves rather than the inhibition of mitochondrial respiration in the light, and that CO2 produced by mitochondrial respiration in the light is mostly emitted at low CO2, and mostly refixed at elevated CO2. In the leaves of the C4 species Zea mays, the 12CO2 emission in the light also remained low at low CO2, suggesting efficient CO2 refixation associated with sustained photosynthesis in non-photorespiratory conditions. However, Rn was inhibited in CO2-free air, and the velocity of 12CO2 emission after darkening was inversely associated with the CO2 concentration. The emission may be modulated by the presence of post-illumination CO2 uptake deriving from temporary imbalance between C3 and C4 metabolism. These experiments suggest that this uptake lasts longer at low CO2 and that the imbalance is persistent once it has been generated by exposure to low CO2.     

CO2和1-MCP组合处理对磨盘柿贮藏效果的影响

以磨盘柿采后果实为材料,研究1-MCP的处理以及CO2脱涩与1-MCP组合处理对磨盘柿室温和0~1℃贮藏过程中果实硬度、可溶性单宁含量、总抗坏血酸(TAA)含量以及抗氧化活性的影响。结果显示:(1)贮藏过程中柿果实硬度随时间延长呈下降趋势,室温贮藏CO2处理5 d、CO2处理后进行1-MCP(CO2//1-MCP)处理10 d、1-MCP处理后进行CO2(1-MCP//CO2)处理15 d、CO2与1-MCP同时(CO2+1-MCP)处理30 d均完全软化,0~1℃贮藏75 d后硬度最高的是CO2+1-MCP处理(12.43 kg.cm-2),最低的是CO2//1-MCP处理(2.80 kg.cm-2),甚至低于CO2处理(5.71 kg.cm-2);(2)柿果实可溶性单宁和总抗坏血酸(TAA)含量与脱涩有关,CO2处理、CO2//1-MCP处理、1-MCP//CO2处理和CO2+1-MCP处理大幅低于CK和1-MCP处理,1-MCP处理抑制了可溶性单宁和TAA含量的下降;(3)室温贮藏中除CO2处理之外的处理柿果实总酚含量呈小幅上升趋势,0~1℃贮藏中CK、1-MCP处理、1-MCP//CO2处理和CO2+1-MCP处理的总酚含量稳定在9.91~12.38 mg.g-1FW之间,CO2处理和CO2//1-MCP处理于30 d之后迅速下降,至75 d时分别只有6.83和6.32 mg.g-1FW;(4)各组处理柿果实ABTS自由基清除能力和氧自由基清除能力值(ORAC)的变化趋势与总酚含量大致相当。研究发现,1-MCP能有效阻止磨盘柿果实贮藏期间的硬度、可溶性单宁含量、TAA含量以及抗氧化活性的下降,CO2脱涩与1-MCP处理的不同顺序对硬度和抗氧化活性影响巨大,但对可溶性单宁和TAA含量影响甚微;先CO2脱涩后1-MCP处理对磨盘柿贮藏效应影响不大,1-MCP处理和高浓度CO2脱涩同时进行是磨盘柿脱涩保鲜的最优方案。