李 白,高廣春,方 琪,李 軍,*
(1.浙江省嘉興市農(nóng)業(yè)科學(xué)研究院(所),浙江 嘉興 314016; 2.嘉興學(xué)院 醫(yī)學(xué)院,浙江 嘉興 314001)
四種蔬菜食用器官提取物對(duì)植物組培污染細(xì)菌的抑制作用
李 白1,高廣春2,方 琪2,李 軍1,*
(1.浙江省嘉興市農(nóng)業(yè)科學(xué)研究院(所),浙江 嘉興 314016; 2.嘉興學(xué)院 醫(yī)學(xué)院,浙江 嘉興 314001)
以生姜、洋蔥、大蒜和苦瓜的食用器官為提取材料,分別用熱水浸提、水超聲提取、乙醇超聲提取和揮發(fā)油提取的方法獲得植物粗提物,探討這些提取物對(duì)組培生產(chǎn)中污染細(xì)菌的抑制作用。抑菌試驗(yàn)結(jié)果表明,4種植物粗提物對(duì)分離的組培污染細(xì)菌均有一定的抑制效果,單種植物提取物不能抑制試驗(yàn)中所有細(xì)菌,不同提取方法獲得的粗提物抑菌效果也有差別。熱水浸提、水超聲提取和乙醇超聲提取方法中,乙醇超聲提取物抑菌效果較好。大蒜和生姜揮發(fā)油對(duì)假單胞菌屬(B2)及腸桿菌屬(B11)菌株有顯著抑菌效果,而其他提取方法無顯著效果。最小抑菌濃度(MIC)結(jié)果表明,大蒜乙醇超聲提取物MIC值較其他提取物低,生姜和大蒜揮發(fā)油效果較好,其對(duì)應(yīng)的鮮質(zhì)量也較高。這一結(jié)果可為植物組培污染菌的防治提供參考。
植物提取物;組織培養(yǎng);細(xì)菌;最小抑菌濃度
植物組織培養(yǎng)的污染問題是影響組培生產(chǎn)的最大障礙之一,它直接影響生產(chǎn)成本和珍貴外植體材料的保全。植物組培污染微生物主要為細(xì)菌和真菌,其中細(xì)菌占50%以上,主要為芽孢桿菌屬和假單胞桿菌屬[1]。為控制細(xì)菌污染,除在組織培養(yǎng)操作過程中控制人為及環(huán)境因素外,在培養(yǎng)基中添加抗生素等抑菌劑也是常用的手段。然而,抗生素的藥物殘留及環(huán)境污染問題,尤其是在食用材料組織培養(yǎng)中的添加,一直是極具爭(zhēng)議的問題。
植物源抑菌劑易降解,靶生物不易產(chǎn)生抗性,對(duì)人畜等非靶標(biāo)生物毒性低,符合現(xiàn)代農(nóng)業(yè)發(fā)展要求,在替代抗生素及減少抗生素應(yīng)用方面具有很大應(yīng)用價(jià)值,近年來成為國(guó)內(nèi)外研究的熱點(diǎn)[2-6]。目前,植物源抑菌劑在植物上的應(yīng)用主要側(cè)重于對(duì)植物病原真菌的防治,對(duì)植物組培污染防治方面的研究較少。崔剛等[7]在國(guó)內(nèi)較早采用植物提取液作為抑菌劑,開展開放組培的研究,建立了葡萄莖段的開放組培體系,獲得的組培苗根系較傳統(tǒng)方式發(fā)達(dá)。張薪薪[8]比較了5種中草藥提取物對(duì)植物組培污染菌的抑制作用,發(fā)現(xiàn)苦參提取物對(duì)細(xì)菌的抑制作用最強(qiáng)。陳瑞丹等[9]以植物源混合粗提液作為抑菌劑,初步建立了梅花莖段的開放式啟動(dòng)培養(yǎng)體系。在組培過程中,植物源抑菌劑毒副作用小,抗菌的同時(shí)可以確保安全,在控制植物組培污染方面具有較大應(yīng)用價(jià)值[10]。
為研究植物源抑菌劑對(duì)植物組培污染細(xì)菌的抑制作用,本研究以生姜、洋蔥、大蒜及苦瓜4種蔬菜的食用器官為材料,采用不同的提取方法獲得植物提取物,研究不同植物及不同提取方法獲得的提取物對(duì)組培生產(chǎn)中污染細(xì)菌的抑制效果,篩選有效的植物源抑菌劑。
1.1 試驗(yàn)材料
植物組培污染細(xì)菌采集自嘉興中瑞生物科技有限公司植物組培間,由本實(shí)驗(yàn)室分離鑒定后,-80 ℃保存,供試細(xì)菌菌株見表1。大蒜、苦瓜、生姜、洋蔥于超市采購(gòu)。
表1植物組培污染細(xì)菌
Table1Pollution bacteria in plant tissue culture
編號(hào)No.細(xì)菌菌屬Bacteriagenera菌株顏色ColorofstrainsB1類芽孢桿菌屬Paenibacillus黃綠色Yellow-greenB2假單胞菌屬Pseudomonas黃綠色Yellow-greenB3不動(dòng)桿菌屬Acinetobacter黃綠色Yellow-greenB4假單胞菌屬Pseudomonas黃色YellowB5芽孢桿菌屬Bacillus橙色OrangeB6芽孢桿菌屬Bacillus黃綠色Yellow-greenB7寡養(yǎng)單胞菌屬Stenotrophomonas黃綠色Yellow-greenB8芽孢桿菌屬Bacillus黃色YellowB9芽孢桿菌屬Bacillus黃色YellowB10埃希氏菌屬Escherichia黃綠色YellowB11腸桿菌屬Enterobacter黃綠色Yellow-GreenB12假單胞菌屬Pseudomonas黃色Yellow
1.2試驗(yàn)方法
1.2.1 提取物制備
水超聲提取:取新鮮大蒜鱗莖、苦瓜果實(shí)、生姜根莖、洋蔥鱗莖,分別切碎后加適量純水,用閃式提取器處理(80 V,2 min);40 KHz 100 W超聲處理30 min,處理液3 000g離心10 min,沉淀加100 mL純水重復(fù)超聲處理30 min,合并上清液;80 ℃濃縮至稠浸膏,稱量,4 ℃保存。
乙醇超聲提?。禾崛》椒ㄍ曁幚恚崛∪軇?0%乙醇。
熱水浸提:取新鮮大蒜鱗莖、苦瓜果實(shí)、生姜根莖、洋蔥鱗莖,分別切碎后加適量純水,用閃式提取器處理(80 V,2 min);沸水浴回流提取2 h,處理液3 000g離心10 min,取上清液;80 ℃濃縮至稠浸膏,稱量,4 ℃保存。
揮發(fā)油提?。喝⌒迈r大蒜鱗莖、苦瓜果實(shí)、生姜根莖、洋蔥鱗莖,分別切碎后加適量純水,用閃式提取器處理(80 V,2 min);轉(zhuǎn)入500 mL圓底燒瓶中,利用揮發(fā)油提取裝置,提取收集揮發(fā)油,計(jì)量,4 ℃保存。
水超聲提取、乙醇超聲提取及熱水浸提物用純水溶解配置成10%(m/V)抑菌劑,揮發(fā)油用0.5% tween-20配置成1%(V/V)抑菌劑。抑菌劑均用0.22 μm濾膜過濾除菌。提取物種類見表2。
表2提取物種類編號(hào)
Table2No. of plant extracts
編號(hào)No.植物材料Plantmaterial提取方法Extractionmethod編號(hào)No.植物材料Plantmaterial提取方法ExtractionmethodGa1大蒜Garlic水超聲提取UltrasonicwaveextractionwithwaterGi1生姜Ginger水超聲提取UltrasonicwaveextractionwithwaterGa2大蒜Garlic熱水浸提HotwaterextractionGi2生姜Ginger熱水浸提HotwaterextractionGa3大蒜Garlic乙醇超聲提取UltrasonicwaveextractionwithethanolGi3生姜Ginger乙醇超聲提取UltrasonicwaveextractionwithethanolGa4大蒜Garlic揮發(fā)油提取VolatileoilextractionGi4生姜Ginger揮發(fā)油提取VolatileoilextractionOn1洋蔥Onion水超聲提取UltrasonicwaveextractionwithwaterGo1苦瓜Bittergourd水超聲提取UltrasonicwaveextractionwithwaterOn2洋蔥Onion熱水浸提HotwaterextractionGo2苦瓜Bittergourd熱水浸提HotwaterextractionOn3洋蔥Onion乙醇超聲提取UltrasonicwaveextractionwithethanolGo3苦瓜Bittergourd乙醇超聲提取UltrasonicwaveextractionwithethanolOn4洋蔥Onion揮發(fā)油提取VolatileoilextractionGo4苦瓜Bittergourd揮發(fā)油提取Volatileoilextraction
1.2.2 抑菌活性測(cè)定
牛津杯法測(cè)定抑菌活性:牛津杯規(guī)格Φ7.8 mm×6.0 mm×10.0 mm(外徑×內(nèi)徑×高),121 ℃高壓滅菌,烘干冷卻備用。將組培污染細(xì)菌(表1)分別涂布在固體LB培養(yǎng)基表面,每個(gè)平皿含有200 μL 106cfu·mL-1測(cè)試細(xì)菌。將牛津杯放入各個(gè)培養(yǎng)基表面,取抑菌劑溶液(表2)200 μL加入牛津杯,30 ℃培養(yǎng)48 h。每組3個(gè)重復(fù),測(cè)定抑菌圈直徑大小,取平均值。
液體倍比稀釋法測(cè)定最低抑菌濃度(minimum inhibition concentration, MIC):將抑菌劑用LB液體培養(yǎng)基分別稀釋成2×、4×、8×、16×、32×、64×濃度,終體積為2 mL,用2 mL LB液體培養(yǎng)基作陽(yáng)性對(duì)照,2 mL 2×稀釋濃度抑菌劑作陰性對(duì)照。取對(duì)數(shù)生長(zhǎng)期污染細(xì)菌懸液40 μL加入倍比稀釋培養(yǎng)基及陽(yáng)性對(duì)照培養(yǎng)基,30 ℃、120 r·min-1培養(yǎng)24 h。每組設(shè)3個(gè)重復(fù),以完全沒有菌生長(zhǎng)的最低提取物濃度為最低抑菌濃度(MIC)。
2.1 植物提取物制備
提取物制備結(jié)果(表3)表明,生姜、洋蔥、大蒜和苦瓜4種植物中,大蒜粗提浸出物最多,洋蔥提取物次之,生姜提取物最少,大蒜提取物質(zhì)量達(dá)到生姜提取物的10倍。乙醇超聲提取方法最好,提取效果好于水超聲提取,浸出物質(zhì)量最大,200 g大蒜樣品通過乙醇超聲提取可獲得55.20 g提取物。揮發(fā)油提取中,大蒜和生姜均獲得少量植物精油,本試驗(yàn)未從洋蔥和苦瓜中獲得植物精油,其揮發(fā)物溶解于水相中。
表3植物粗提物的提取效果
Table3Extraction effect of crude extracts from plants
植物Plants水超聲提取Ultrasonicwaveextractionwithwater提取物質(zhì)量Extractweight/g1mL10%抑菌劑含鮮質(zhì)量Freshweightin1mL10%bacteriostaticagent/g乙醇超聲提取Ultrasonicwaveextractionwithethanol提取物質(zhì)量Extractweight/g1mL10%抑菌劑含鮮質(zhì)量Freshweightin1mL10%bacteriostaticagent/g熱水浸提Hotwaterextraction提取物質(zhì)量Extractweight/g1mL10%抑菌劑含鮮質(zhì)量Freshweightin1mL10%bacteriostaticagent/g揮發(fā)油提取Volatileoilextraction揮發(fā)物體積Volatilevolume/mL1mL1%抑菌劑含鮮質(zhì)量Freshweightin1mL1%bacteriostaticagent/g大蒜Garlic37.420.5355.200.3643.370.461.258.00生姜Ginger3.715.395.483.653.865.180.8511.76洋蔥Onion12.271.6317.711.1315.381.3038.002.63苦瓜Bittergourd5.833.435.293.785.143.8921.004.76
注:熱水浸提、水超聲提取、乙醇超聲提取各樣品鮮質(zhì)量均為200 g,揮發(fā)油提取各樣品鮮質(zhì)量均為1 000 g
Note: Fresh weight of all the samples extracted by hot water extraction, ultrasonic wave extraction with water or ethanol were 200 g, and fresh weight of all the samples extracted by volatile oil were 1 000 g
2.2 提取物抑菌活性
提取物抑菌活性測(cè)定時(shí),水超聲提取、乙醇超聲提取及熱水浸提物配制成10%(m/V)濃度,揮發(fā)油配制成1%(V/V)濃度;由于大蒜提取物最多,具有抑菌活性的抑菌劑含鮮質(zhì)量也最低(表3)。4種植物粗提物抑菌活性測(cè)定結(jié)果(表4)表明,大蒜乙醇超聲提取物、生姜乙醇超聲提取物、洋蔥乙醇超聲、洋蔥熱水浸提物、苦瓜水超聲提取物、苦瓜乙醇超聲提取物對(duì)4株芽孢桿菌屬菌株具有較強(qiáng)抑制效果;生姜熱水浸提物、洋蔥乙醇超聲提取物對(duì)2株假單胞菌屬菌株具有較強(qiáng)抑制效果;洋蔥提取物、苦瓜超聲提取物、生姜揮發(fā)油、大蒜揮發(fā)油對(duì)2株腸桿菌屬菌株具有較強(qiáng)抑菌效果。B1、B2、B3、B7菌株對(duì)4種植物提取物敏感性均較低。4種植物中,洋蔥提取物能有效抑制5種細(xì)菌生長(zhǎng),包括3種芽孢桿菌屬菌株、1種假假單胞菌、1種腸桿菌。生姜揮發(fā)油、大蒜揮發(fā)油對(duì)假單胞菌屬(B2)及腸桿菌屬(B11)細(xì)菌有顯著抑菌效果,而其他粗提物的抑菌效果不顯著。圖1為部分植物提取物的抑菌效果。
2.3最低抑菌濃度測(cè)定
根據(jù)提取物抑菌活性結(jié)果,選取4種植物乙醇超聲提取物及生姜揮發(fā)油、大蒜揮發(fā)油,測(cè)定抑制效果較好的細(xì)菌菌株的MIC。結(jié)果(表5)表明,大蒜和生姜揮發(fā)油的MIC值最低,在稀釋倍數(shù)分別為1 600倍[浸出物0.0625%(V/V),鮮質(zhì)量含量0.5 g·mL-1]和800倍[浸出物0.125%(V/V),鮮質(zhì)量含量1.47 g·mL-1]時(shí),對(duì)腸桿菌屬B5仍具有抑菌效果,較低稀釋倍數(shù)下對(duì)其他試驗(yàn)菌株也有一定抑制效果。若以鮮質(zhì)量為參考標(biāo)準(zhǔn),則大蒜粗提物MIC值較低,稀釋倍數(shù)為40倍(浸出物0.025 g·mL-1,鮮質(zhì)量含量0.12 g·mL-1)和20倍(浸出物0.05 g·mL-1, 鮮質(zhì)量含量0.23 g·mL-1)時(shí),分別對(duì)B8、B6和B9具有抑制作用。與揮發(fā)油MIC值相比,生姜、大蒜、洋蔥乙醇超聲提取物的MIC值較高,原因可能是揮發(fā)油提取物樣品的濃縮倍數(shù)高,且揮發(fā)油中含有的化合物抑菌作用較強(qiáng)。比較MIC與抑菌活性試驗(yàn)結(jié)果可知,除洋蔥外,其他抑菌劑MIC與抑菌活性試驗(yàn)結(jié)果較一致,而洋蔥乙醇超聲提取物在抑菌活性試驗(yàn)中具有較強(qiáng)的抑菌效果,但在MIC試驗(yàn)中,抑菌效果達(dá)不到預(yù)期,這可能與培養(yǎng)基的物理形態(tài)改變有關(guān),尚需進(jìn)一步研究。圖2為Go3提取物對(duì)B1菌株最低抑菌濃度的測(cè)定。
表4植物提取物的抑菌活性
Table4Antibacterial activity of plant extracts
菌株Bacterialstrains提取物抑菌活性AntibacterialactivityofplantextractsGa1Ga2Ga3Ga4Gi1Gi2Gi3Gi4On1On2On3On4Go1Go2Go3Go4B1-----+---------+B2-------+--------B3----++----+--++-B4-----++--+-------B5--++++++---++++++-----B6-+++---++--+++++++-++---B7----+--++-------B8--++---+++++++--++-B9+--++---+--++-+-++-B10--+-----++++++++++++-++B11---++---++--------B12+---------+++--+--
“-”,抑菌圈直徑<9 mm,不敏感;“+”,抑菌圈直徑9~10 mm,輕度敏感;“++”,抑菌圈直徑10~15 mm,中度敏感;“+++”,抑菌圈直徑15~20 mm,高度敏感;“++++”,抑菌圈直徑>20 mm, 極敏感。
“-”, Diameter of inhibition zone is less than 9 mm, insensitivity; “+”, Diameter of inhibition zone is 9-10 mm, slight sensitive; “++”, Diameter of inhibition zone is 10-15 mm, moderately sensitive; “+++”, Diameter of inhibition zone is 15-20 mm, highly sensitive; “++++”, Diameter of inhibition zone is more than 20 mm, extremely sensitive.
B6、B11及B3為分離到的植物組培污染細(xì)菌,詳見表1;On2、Gi4及Go1為植物提取物,詳見表2B6, B11 and B3 were bacteria isolated from plant tissue culture, as shown in Table 1; On2, Gi4 and Go1 were plant extracts, as shown in Table 2圖1 部分植物提取物的抑菌效果Fig.1 Bacteriostatic effect of partial plant extracts
表5提取物對(duì)部分菌株的最低抑菌濃度
Table5Minimum inhibitory concentration of plant extracts against to partial bacterial strains g·mL-1
菌株Bacterialstrains植物提取物最低抑菌濃度MinimuminhibitoryconcentrationofplantextractsGa3Ga4Gi3Gi4On3Go3B1—————0.025(0.97)B5—0.000625(0.50)—0.00125(1.47)——B60.05(0.23)0.005(4.00)0.05(>2.59)0.005(>5.88)0.05(>0.65)0.025(0.97)B80.025(0.12)—0.025(1.30)——0.0125(0.49)B90.05(0.23)0.005(4.00)—0.005(5.88)0.05(>0.65)0.025(0.97)B11—0.0025(2.00)—0.005(5.88)——B12—0.005(4.00)——0.05(>0.65)—
Ga4、Gi4最低抑菌濃度為體積比;“—”為未進(jìn)行試驗(yàn);“>”為MIC超過本試驗(yàn)濃度上限;“( )”內(nèi)數(shù)值為最低抑菌濃度對(duì)應(yīng)的樣品鮮質(zhì)量濃度。
MIC of Ga4 and Gi4 were displayed by volume ratio; “—” indicated experiment was not carried out; “>” indicated MIC was above test concentration limit; Data in “()” was the sample fresh weight concentration corresponded to the MIC.
圖2 Go3提取物對(duì)B1菌株最低抑菌濃度測(cè)定Fig.2 Determination of minimum inhibitory concentration of Go3 extract against to B1 strain
3.1植物源抑菌劑的優(yōu)勢(shì)
植物組織培養(yǎng)中細(xì)菌污染主要通過接觸污染,如外植體帶菌、人員操作不當(dāng)或器械消毒不嚴(yán)格等??刂浦参锝M培細(xì)菌污染除了定期嚴(yán)格的人員、環(huán)境消毒、操作流程的規(guī)范以及選擇無菌的外植體等途徑外,在培養(yǎng)基中添加一定濃度的抗生素,如青霉素、鏈霉素、四環(huán)素及硫酸慶大霉素等也能獲得一定的抑菌效果[11-12]。然而,抗生素殘留、環(huán)境污染、部分抗生素價(jià)格昂貴、傷害組培苗等問題一直制約著植物組織培養(yǎng)中抗生素的添加。
與抗生素相比,植物源抑菌劑具有低毒、低殘留、對(duì)組培苗傷害小及與環(huán)境相容等優(yōu)勢(shì)。王趙玉等[13]研究表明,適當(dāng)濃度的大蒜素與代森錳鋅均能降低組培試驗(yàn)污染率,且不會(huì)對(duì)植物產(chǎn)生不利影響。曾云英等[14]發(fā)現(xiàn)植物源與化學(xué)合成的抑菌劑在矮牽牛開放組培中均有良好作用,化學(xué)合成抑菌劑較植物源抑菌劑效果強(qiáng),但對(duì)植物傷害較大。據(jù)報(bào)道,國(guó)內(nèi)外有1 000余種植物被檢測(cè)出有殺菌活性,國(guó)內(nèi)的研究熱點(diǎn)主要集中在連翹、板藍(lán)根、苦參及魚腥草等中草藥植物。本研究以生姜、洋蔥、大蒜和苦瓜為提取材料,4種植物材料相對(duì)于中草藥具有低成本及材料易獲取等優(yōu)勢(shì)。目前,植物源抑菌劑的應(yīng)用主要集中在對(duì)植物病原真菌的防治,有關(guān)植物組培污染細(xì)菌防治方面的研究較少,本研究為植物源抑菌劑在植物組培污染細(xì)菌防治方面的應(yīng)用提供了參考。
3.2 四種植物提取物的抑菌活性
據(jù)報(bào)道,生姜、洋蔥、大蒜和苦瓜4種植物對(duì)多種植物病原菌及細(xì)菌具有較好的抑制效果。國(guó)淑梅等[15]研究發(fā)現(xiàn),大蒜及生姜提取液對(duì)平菇生產(chǎn)中常見的3種芽孢桿菌屬細(xì)菌均有抑制作用。楊敏等[16]測(cè)定了大蒜、洋蔥和蔥莖揮發(fā)物及提取液對(duì)26種主要植物病原真菌和卵菌的抑制活性,發(fā)現(xiàn)大蒜、洋蔥和蔥莖的揮發(fā)物和浸提液具有廣譜抗植物病原真菌和卵菌的活性。文良娟等[17]研究表明,苦瓜70%乙醇提取物對(duì)大腸埃希菌、金黃色葡萄球菌及枯草芽孢桿菌的抑制作用明顯。
本研究抑菌試驗(yàn)結(jié)果表明,大蒜乙醇超聲粗提物、大蒜揮發(fā)油和生姜揮發(fā)油對(duì)污染菌株具有較好的抑制效果,生姜、洋蔥、苦瓜的乙醇超聲提取物較水超聲提取、熱水浸提法的綜合抑菌效果強(qiáng)。洋蔥粗提物對(duì)12個(gè)菌株中的9個(gè)菌株有抑制效果,抗菌譜較生姜、大蒜、苦瓜提取物廣。不同菌株對(duì)不同抑菌劑的敏感程度不同,復(fù)配使用可以提高效果[18-19]。本研究結(jié)果表明,單種植物抑菌劑對(duì)不同菌株抑制作用存在差異,不同植物抑菌劑的抗菌譜存在互補(bǔ)作用,因此,在植物組培中采用單一抑菌劑可能達(dá)不到最佳效果,如果將其復(fù)配成混合抑菌劑,可以提升抗菌譜范圍,增強(qiáng)抑菌效果。
3.3 提取方法對(duì)抑菌活性的影響
不同提取方法對(duì)提取物抑菌活性具有顯著影響。穆可云[20]研究了大蒜水提取物、乙醇提取物及酸性水溶液提取物對(duì)蠟樣芽孢桿菌的抑制效果,發(fā)現(xiàn)3種提取物都有抑制效果,并且抑菌效果依次增強(qiáng)。溫度穩(wěn)定性試驗(yàn)結(jié)果表明,高溫處理會(huì)降低洋蔥粗提物的抑菌能力[21-22]。本研究表明,生姜揮發(fā)油對(duì)假單胞菌屬(B2)有抑制效果,而生姜水超聲提取、熱水浸提、乙醇超聲提取粗提物對(duì)假單胞菌屬(B2)均無抑制效果,這說明提取方式影響植物抑菌活性物質(zhì)的溶解性或穩(wěn)定性。本試驗(yàn)中,乙醇超聲提取較熱水浸提、水超聲提取方法更能溶解出抑菌物質(zhì),揮發(fā)油與溶劑提取物具有不同的抑菌譜。聯(lián)合不同方法綜合提取抑菌物質(zhì),可以更大潛力地發(fā)掘植物抑菌物,如溶劑提取同時(shí)聯(lián)合揮發(fā)物收集裝置,可獲得更多抑菌活性物質(zhì),其抗菌譜也更廣。
與前人研究相比,本研究中抑菌劑的MIC值偏高[23-24],可能是提取物濃縮過程破壞了部分抑菌物質(zhì),尤其是苦瓜粗提物濃縮后再溶解不完全,沉淀明顯,也可能是本研究的菌株是從被污染組培植物中分離的,這些菌株可能對(duì)部分植物源抑菌物不敏感。后續(xù)研究可進(jìn)一步明確植物源抑菌劑的作用機(jī)理,開發(fā)聯(lián)合提取方法,采用復(fù)配抑菌劑,將擴(kuò)大植物抑菌劑的抗菌譜,提升抑菌效果。
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(責(zé)任編輯侯春曉)
Inhibitionoffourvegetableedibleorganextractsonbacterialcontaminationinplanttissueculture
LI Bai1, GAO Guangchun2, FANG Qi2, LI Jun1,*
(1.JiaxingAcademyofAgriculturalSciences,Jiaxing314016,China; 2.SchoolofMedicineScience,JiaxingUniversity,Jiaxing314001,China)
Plant extracts were obtained from four vegetable edible organs including ginger rhizome, onion bulb, garlic bulb and bitter gourd fruit. The extraction methods were hot water extraction, ultrasonic wave extraction with water, ultrasonic wave extraction with ethanol, volatile oil extraction. Inhibition of these extracts on bacterial contamination in the production of tissue culture were discussed. The results showed that the crude extracts from the four plants had inhibition on the bacteria while single plant extracts could not inhibit all the bacteria. Crude extracts obtained by different extraction methods had different antimicrobial effects. Ultrasonic wave extraction with ethanol had the best antibacterial effect among the three solvent extraction methods. The essential oil from garlic and ginger could significantly inhibitPseudomonas(B2) andEnterobacter(B11), and other extracts had no significant inhibition. Minimum inhibitory concentration results showed that the MIC value of crude extract from garlic using ultrasonic wave extraction with ethanol was lower than those of other extracts, ginger and garlic essential oil had low MIC value and higher fresh weight. This research could provide references for the prevention and control of bacterial contamination in plant tissue culture.
plant extracts; plant tissue culture; bacteria; minimum inhibitory concentration
李白, 高廣春, 方琪, 等. 四種蔬菜食用器官提取物對(duì)植物組培污染細(xì)菌的抑制作用[J]. 浙江農(nóng)業(yè)學(xué)報(bào), 2017, 29(11): 1854-1861.
10.3969/j.issn.1004-1524.2017.11.11
2017-05-19
嘉興市科技計(jì)劃項(xiàng)目(2016BY26005)
李白(1986—),男,浙江溫州人,碩士,農(nóng)藝師,主要從事植物生物技術(shù)研究。E-mail: libaia@yeah.net
*通信作者,李軍,E-mail: lijunjx1@163.com
S188
A
1004-1524(2017)11-1854-08