JP2011121878A - 植物の抽苔抑制剤 - Google Patents
植物の抽苔抑制剤 Download PDFInfo
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- JP2011121878A JP2011121878A JP2009279084A JP2009279084A JP2011121878A JP 2011121878 A JP2011121878 A JP 2011121878A JP 2009279084 A JP2009279084 A JP 2009279084A JP 2009279084 A JP2009279084 A JP 2009279084A JP 2011121878 A JP2011121878 A JP 2011121878A
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- acid
- vegetables
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- 239000003112 inhibitor Substances 0.000 title claims abstract description 11
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- 150000003839 salts Chemical class 0.000 claims abstract description 19
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- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 11
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- 125000002252 acyl group Chemical group 0.000 claims abstract description 8
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 235000010382 gamma-tocopherol Nutrition 0.000 description 1
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- 235000004611 garlic Nutrition 0.000 description 1
- IXORZMNAPKEEDV-UHFFFAOYSA-N gibberellic acid GA3 Natural products OC(=O)C1C2(C3)CC(=C)C3(O)CCC2C2(C=CC3O)C1C3(C)C(=O)O2 IXORZMNAPKEEDV-UHFFFAOYSA-N 0.000 description 1
- 239000003448 gibberellin Substances 0.000 description 1
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- 239000008103 glucose Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
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- UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 description 1
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- FYGDTMLNYKFZSV-UHFFFAOYSA-N mannotriose Natural products OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(OC2C(OC(O)C(O)C2O)CO)C(O)C1O FYGDTMLNYKFZSV-UHFFFAOYSA-N 0.000 description 1
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- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
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- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- CAAULPUQFIIOTL-UHFFFAOYSA-N methyl dihydrogen phosphate Chemical compound COP(O)(O)=O CAAULPUQFIIOTL-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- 125000005447 octyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
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- 229940055726 pantothenic acid Drugs 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
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- 229960003330 pentetic acid Drugs 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- XVNIJEYEHHBPPR-UHFFFAOYSA-N pentyl 5-amino-4-oxopentanoate Chemical compound CCCCCOC(=O)CCC(=O)CN XVNIJEYEHHBPPR-UHFFFAOYSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
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- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
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- MBWXNTAXLNYFJB-LKUDQCMESA-N phylloquinone Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CCCC(C)CCCC(C)CCCC(C)C)=C(C)C(=O)C2=C1 MBWXNTAXLNYFJB-LKUDQCMESA-N 0.000 description 1
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- 230000002035 prolonged effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
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- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- KYELCRMQMAPVJB-UHFFFAOYSA-N propyl 5-amino-4-oxopentanoate Chemical compound CCCOC(=O)CCC(=O)CN KYELCRMQMAPVJB-UHFFFAOYSA-N 0.000 description 1
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- 230000001105 regulatory effect Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
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- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
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Abstract
【解決手段】一般式(1)
R2R1NCH2COCH2CH2COR3 (1)
[式中、R1及びR2は各々独立に、水素原子、アルキル基、アシル基、アルコキシカルボニル基、アリール基又はアラルキル基を示し;R3はヒドロキシ基、アルコキシ基、アシルオキシ基、アルコキシカルボニルオキシ基、アリールオキシ基、アラルキルオキシ基又はアミノ基を示す。〕
で表される5−アミノレブリン酸、その誘導体又はそれらの塩を有効成分とし、葉菜類又は根菜類植物の最適生長栽培条件外で施用するためのものである、葉菜類又は根菜類植物の抽苔抑制剤。
【選択図】なし
Description
また、植物の生長にあたっては、品種によって異なるものの、それぞれ最適な環境要因(栽培条件)があり、例えば、その最適な環境要因よりも、低照度、低温、高温、肥料不足や水分不足、水分過多等の環境ストレスによっても抽苔が起こる場合があることが知られている。
植物工場に代表される室内栽培では、栽培環境を制御でき季節や天候の影響を受けずに栽培できる利点があるが、一方で植物の生育に十分な照度を確保することが難しく低照度条件になり易いため、目的とする葉等が十分生長する前に抽苔が起こる可能性があるという課題がある。また、日照時間を長くすることで生長促進を図ることができるが、ホウレンソウなどの長日植物では、日長条件が長日になると抽苔が起こる。
葉菜類や根菜類では、抽苔により、可食部として利用する葉や根の生長が停止する、または望まれる形態とは異なる形態となり、食味も落ちることで、商品価値が著しく低下する、または失われる。
R2R1NCH2COCH2CH2COR3 (1)
[式中、R1及びR2は各々独立に、水素原子、アルキル基、アシル基、アルコキシカルボニル基、アリール基又はアラルキル基を示し;R3はヒドロキシ基、アルコキシ基、アシルオキシ基、アルコキシカルボニルオキシ基、アリールオキシ基、アラルキルオキシ基又はアミノ基を示す。]
で表される5−アミノレブリン酸、その誘導体又はそれらの塩を有効成分とし、葉菜類又は根菜類植物の最適生長栽培条件外で施用するためのものである、葉菜類又は根菜類植物の抽苔抑制剤を提供するものである。
一般式(1)中、R1及びR2で示されるアルキル基としては、炭素数1〜24の直鎖又は分岐鎖のアルキル基が好ましく、より好ましくは炭素数1〜18のアルキル基、特に炭素数1〜6のアルキル基が好ましい。炭素数1〜6のアルキル基としては、メチル基、エチル基、n−プロピル基、イソプロピル基、n−ブチル基、sec−ブチル基等が挙げられる。
R1及びR2で示されるアシル基としては、炭素数1〜24、好ましくは炭素数1〜12の直鎖又は分岐鎖のアルカノイル基、アルケニルカルボニル基、アロイル基又はアリールオキシカルボニル基が好ましく、特に炭素数1〜6のアルカノイル基が好ましい。当該アシル基としては、ホルミル基、アセチル基、プロピオニル基、ブチリル基、n−ペンタノイル基、n−ヘキサノイル基、n−ノナノイル基、ベンジルオキシカルボニル基等が挙げられる。
R1及びR2で示されるアルコキシカルボニル基としては、総炭素数2〜13のアルコキシカルボニル基が好ましく、特に炭素数2〜7のアルコキシカルボニル基が好ましい。当該アルコキシカルボニル基としては、メトキシカルボニル基、エトキシカルボニル基、n−プロポキシカルボニル基、イソプロポキシカルボニル基等が挙げられる。
R1及びR2で示されるアリール基としては、炭素数6〜16のアリール基が好ましく、例えば、フェニル基、ナフチル基等が挙げられる。
R1及びR2で示されるアラルキル基としては、炭素数6〜16のアリール基と上記炭素数1〜6のアルキル基とからなる基が好ましく、例えば、ベンジル基等が挙げられる。
R3で示されるアシルオキシ基としては、炭素数1〜12の直鎖又は分岐鎖のアルカノイルオキシ基が好ましく、特に炭素数1〜6のアルカノイルオキシ基が好ましい。当該アシルオキシ基としては、アセトキシ基、プロピオニルオキシ基、ブチリルオキシ基等が挙げられる。
R3で示されるアルコキシカルボニルオキシ基としては、総炭素数2〜13のアルコキシカルボニルオキシ基が好ましく、特に総炭素数2〜7のアルコキシカルボニルオキシ基が好ましい。当該アルコキシカルボニルオキシ基としては、メトキシカルボニルオキシ基、エトキシカルボニルオキシ基、n−プロポキシカルボニルオキシ基、イソプロポキシカルボニルオキシ基等が挙げられる。
R3で示されるアリールオキシ基としては、炭素数6〜16のアリールオキシ基が好ましく、例えば、フェノキシ基、ナフチルオキシ基等が挙げられる。アラルキルオキシ基としては、前記アラルキル基を有するものが好ましく、例えば、ベンジルオキシ基等が挙げられる。
以上詳述した5−アミノレブリン酸、その誘導体又はそれらの塩は、水和物又は溶媒和物を形成していてもよく、またいずれかを単独で又は2 種以上を適宜組み合わせて用いることができる。
これらのうち、ホウレンソウ、コマツナ、ハクサイ、ダイコン、アブラナが好適であり、特にホウレンソウが好適である。
ここで、植物の最適生長栽培条件とは、生産者には広く知られているものであり、例えば、ホウレンソウであれば、長日植物であるため、日長条件は短日、照度は50,000lx、温度は15〜20℃、栽培期間は40〜70日、肥料量は10a当たり窒素20〜25kg,リン酸10〜15kg,カリウム10〜15kgであるが、日長条件が長日である場合には、照度は100,000lx、温度は15〜20℃、栽培期間は30〜40日、肥料量は10a当たり窒素20〜25kg,リン酸10〜15kg,カリウム10〜15kgであり、最適生長栽培条件外の栽培条件とは、それ以外の栽培条件を指す。最適生長栽培条件中、例えば、照度について最適生長栽培条件を満たしていても温度が最適生長栽培条件を満たしていなければ、最適栽培条件外の栽培条件である、なお、本発明においては、複数の条件が最適栽培条件外であることが好ましい。
また、最適生長栽培条件よりも長日、短日、低照度、低温、高温、長期栽培又は肥料不足の栽培条件とは、植物の種類により相違するが、当該植物の最適生長栽培条件よりも、日長条件については長日植物では長日、短日植物では短日、照度については10〜99.9%低い、温度については5〜15℃低い、もしくは5〜20℃高い、栽培期間については1日以上長い、又は肥料が20〜90%不足している条件が好ましい。
具体的に例を挙げると、ホウレンソウにおいては、照度5,000〜80,000lxが好ましく、さらに好ましくは10,000〜70,000lxが好ましい。
また、生長促進を目的として夜間に人工照明を利用する補光栽培においても同様に使用できる。
温度条件は、低温すなわち0〜15℃または高温すなわち20℃〜40℃が好ましく、より好ましくは0〜10℃または30℃〜40℃であるが、各植物によって異なり、これに限定されない。
ホウレンソウを圃場に播種し慣行法に従い栽培した。土壌は赤土を用いた。個体数は10〜14個体/区、3区/条件とした。
基肥として化成肥料(窒素、リン酸、カリウム各々8%含有)を10a当たり窒素、リン酸、カリウムが各々5kgとなるよう施した。高温を避けるため、播種11日後から17日後までと27日後から33日後(収穫日)まで遮光資材(遮光率31%)を用いて遮光を行った。遮光時の照度は約69,000lxであった。日長は長日条件であり、温度は約25℃であった。
5−アミノレブリン酸塩酸塩処理区においては、播種14日後から概ね1週間ごとに5−アミノレブリン酸塩酸塩を0.006mM含む水溶液を10a当たり100L散布した。
ホウレンソウをポット(上下が仕切られており、上部(面積0.007m2)の土に下部(容量400ml)の水耕液がひもを通じて供給される)に播種し栽培した。土壌は培養土を用い、水耕液は液体肥料(窒素6%、リン酸10%、カリウム5%含有)を窒素成分0.006%含有(栽培途中からは窒素成分0.012%含有)となるよう希釈して用い減少した時に交換した。栽培は室内で、人工照明として、蛍光灯(照度約10,000lx、点灯時間7:00〜18:00)を用いて行った。67日後からは夜間補光(照度3500lx、点灯時間18:00〜23:00)を行った。温度は25℃であった。個体数は、4個体/条件とした。
5−アミノレブリン酸塩酸塩処理区においては、播種36日後から水耕液交換時に5−アミノレブリン酸塩酸塩を0.009mMの濃度となるよう加えた。
コンテナ2個を用意し、それぞれに土を入れ、ホウレンソウの種を均等に植えた。種苗した日から毎日1回じょうろで水を与えた。コンテナの一方に、5−アミノレブリン酸塩酸塩0.006mMを溶かした水道水を霧吹きで1日1回、50mL程度を散布し、種苗から3週間後に間引きを、38日後に2つのコンテナの収穫を行った。個体数は18〜22であった。照度は約95,000lxであった。
その結果、対照区に比べ、5−アミノレブリン酸塩酸塩処理区は抽苔率が82%高かった。
この結果より、照度が95,000lx以上の条件下では、5−アミノレブリン酸を施用しても、抽苔は抑制されないことが分かる。
Claims (5)
- 一般式(1)
R2R1NCH2COCH2CH2COR3 (1)
[式中、R1及びR2は各々独立に、水素原子、アルキル基、アシル基、アルコキシカルボニル基、アリール基又はアラルキル基を示し;R3はヒドロキシ基、アルコキシ基、アシルオキシ基、アルコキシカルボニルオキシ基、アリールオキシ基、アラルキルオキシ基又はアミノ基を示す。〕
で表される5−アミノレブリン酸、その誘導体又はそれらの塩を有効成分とし、葉菜類又は根菜類植物の最適生長栽培条件外で施用するためのものである、葉菜類又は根菜類植物の抽苔抑制剤。 - 最適生長栽培条件外が、最適生長栽培条件よりも、長日、短日、低照度、低温、高温、栽培期間の長期化、又は肥料不足である請求項1記載の抽苔抑制剤
- 植物が、ホウレンソウ、コマツナ、ハクサイ、ダイコン及びアブラナから選ばれるものである請求項1記載の抽苔抑制剤。
- 植物がホウレンソウである請求項1記載の抽苔抑制剤。
- 葉菜類又は根菜類植物の最適生長栽培条件外の栽培条件下で、一般式(1)
R2R1NCH2COCH2CH2COR3 (1)
[式中、R1及びR2は各々独立に、水素原子、アルキル基、アシル基、アルコキシカルボニル基、アリール基又はアラルキル基を示し;R3はヒドロキシ基、アルコキシ基、アシルオキシ基、アルコキシカルボニルオキシ基、アリールオキシ基、アラルキルオキシ基又はアミノ基を示す。〕
で表される5−アミノレブリン酸、その誘導体又はそれらの塩を施用する、葉菜類又は根菜類植物の抽苔抑制方法。
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