plasto globules

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Plant Cell R eports (1982) 1 : 11 I- 11 4 Plant ell Reports © Springer-Verlag 1982 omposition and Molecular Structure of hromoplast Globules of iola ricolor Paul Hansm ann and Peter Sitte Institut ffir Biologie II, Zellbiologie, Universit~t Freiburg, Schii nzlestr af3e 1, D-7800 Freiburg i. Br., Federal Republic of Germany Rece ived Decem ber 7, 1981 ; February 8, 1982 Abstract Plastoglobules have been isolated in pure form from petals of the pansy, V~o~ ~oo~or L. Their chemical composition has been determined up to a recovery of 96% dry weight, Triacyl glycerols (57%) as well as carotenoids and their esters (23%) are the main con- stituents. Polar lipids, proteins, alkanes, phytyl esters, plastid quinones, and steryl esters have been detected in smaller amounts (cf. Table I). The mean diameter of chromoplast globules is 280±70 nm (cor- responding to a volume of 11.7 x Io nm3), their buoy- ant density o.93 g cm 3. The plastoglobules are devoid of a surrounding unit membrane. However, electron mi- croscopical evidence and analytical data are consist- ent with a structural model envisaging the globules to consist mainly of an apolar core, covered by a 'half unit membrane' of polar constituents. Abbreviations: FA, fatty acid; GA, glutardialdehyde; GLC, gas liquid chromatography; TLC, thin-layer chromatography Introduction Chromop asts are plastids devoid of chlorophylls, but pigmented by carotenoids, and occur mainly in flowers and fruits. According to their fine structure, five classes can be distinguished (Sitte 1974), i.e. glob- ulous, tubulous, reticulo-tubulous, membranous, and crystallous chromoplasts. Some of the characteristic internal carotenoid accumulating substructures of chromoplasts have been isolated and characterised in terms of chemical composition (for a recent review, cf. Sitte et al. 1980). Surprisingly, chromoplast globules have not yet been analysed in spite of the fact that the globulous type of chromoplast is by far the most common one and, probably, the most primitive one with regard to phylogeny. Chromoplast globules are typical plastoglobules after the definition of Lichtenthaler (1966, 1968 b; Lich- tenthaler and Sprey 1966). Plastoglobules have been found in all plastid types. They have been isolated from chloroplasts and chromoplasts, and several at- tempts have been undertaken to analyse them qualita- tively or, to a limited extent, quantitatively(Green- wood et al. 1963~ Bailey and Whyborn 1963; Lichten- thaler 1964, 1968 b, 1970; Lichtenthaler and Sprey 1966; Barr et al. 1967; Lichtenthaler and Peveling 1967; Wuttke 1977; Sitte et al. 1980). As expected, plastoglobules are lipid-dominated structures. How- ever, no detailed quantitative analysis on a dry weighC basis has been published so far. The fine structural appearance of plastoglobules has been described repeatedly (cf., e.g., Frey-Wyssling and Kreutzer 1958; Steffen and Walter 1958; Wettstein 1957; Falk 196o; Sitte 1963; Lichtenthaler and Sprey 1966; Wuttke 1977). In the typical case, they are sphergcal inclusions having moderate to strong osmio- philia and often exhibiting a dense surface layer. The real nature of this layer is a matter of controversy (as it is in the case of corresponding lipid droplets in the cytoplasm, differently designated as spherosomes or oleosomes - cf. Sitte 1981). The purpose of the present study was to ascertain, in quantitative terms, the chemical composition of plasto- globules from flower chromoplasts of Z~o~ t~o0~or and to unravel the nature of their surface layer. Material and Methods Plant Material, Fractionation: Pansies Z~o~a ~oo~0~ L. Ssp. maxima; "Mausers Goldelse gelb, ohne Auge") were cultivated outdoors. 5o g of petals were chopped with a razor blade in ice-cold isolation medium (15% [w/v] sucrose; 66 mM phosphate buffer, pH 7.4) in por- tions of io g tissue per 5o ml, and were homogenised with a knife homogeniser (B@hler, T@bingen, FRG; 4 x 4 s, i/3 maximum speed). After filtration through 3 layers of nylon cloth the filtrate was centrifuged (3oo g; io min ). The supernatant was sonicated in o ml aliquots and centrifuged in an ultracentrifuge (ioo,ooo g, 9o min). The floating pad was purified by a further flotation using a discontinous sucrose gra- dient [aq. dest., 7.5%, 15% (w/v) sucrose, 66 mM phos- phate buffer, pH 7.4], at 8o,ooo ~ for 9o min. The plastoglobules, concentrated on top of the gradient, were removed and dialysed against aq. dest. 2 x I, 3, and 14 h, respectively). The dialysed plastoglobules as well as a corresponding aliquot of the dialysis me- dium were lyophilized; the weight difference was taken as the dry weight of the plastoglobule fraction. Qualitative Analyses: Separation of proteins was car- ried out in an SDS-PAGE system as described previ- ously (Liedvogel et al. 1976). Lipids were extracted according to Folch et al. (1957). For some experiments, lipids were saponified with ethanolic KOH (9% w/v). AI- kanes and esters were separated by TLC (Kieselgel 6o F 54' Merck Darmstadt, FRG) using CCl as a solvent (Hol~oway and Challen 1966), plastoquinones with CC14/ CHCl 3 (2/3; Lichtenthaler 1977), carotenoid esters 0721-7714/82/0001/0111/ 01.00

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with petrol (4o-6o °C)/die thyl ether /a cetone (1o/2/1) ;phytol , s terols , and quinone s with CHCI~; methyl-

o Jes ters of FAs with petrol (4o-6o C)/die thyl ether(35/2o); FAs with CHCl~ /e thy laee ta t e / fo rma te (4o/6/3;cf. Kati ng et al . 197o~; and the polar l ip i d f ract ionus ing the 2-dimens ional sys tem of Allen and Good (1971) .Rou t in e ly th e l ip id s po t s w er e de tec ted by s p r ay ingwith Rhodamin- Tinop al (Popov and Stefan ov 1968),w her eas th e p la s toqu in on es w er e v i s ua l i s ed by theEmmer ie-Eng els re agent (Barr and Crane 1971) , and thes teroids and phytol by the Car t-P r ice rea gent (Neherand Wetts tein 1951) . Separat ion of caroten oids (af terhydrol s is of carotenoi d es ters) took place on cel lu-lose th in layers (Merck, impreg nated by a t r iacyl g ly-cerol phase) with methano l / ace tone /HgO (15/5/i) assolvent (Egger 1962) . Individual l ip i ds were ident i-f i ed by co - ch r omatog r aph y o f au then t i c r e f e r ence s ub -s t ances an d b y comb in a t io n o f TLC and G LC. G LC w asus ed to id en t i f y the me thy l e s t e r s o f co r r e s po nd ingFAs ( io EGSS-X, Gasch rom P, 125-15o mesh) as wellas phytol (3 Poly A io3, Gaschrom Q, Ioo/12o mesh) .

Q uan t i t a t iv e A na ly s es : Co mmon FA s w er e de te r minedaccord ing to Duncomb e (1963) , whereas the amount of~ - hyd r o x y FA s w as ca lcu la t ed f r om the i r r e l a t ive p r o -po r t io n s on gas - l iqu id ch r o matog r ams . The amoun t s o f

po la r l i p id s w er e de te r min ed v ia the i r f a t ty ac idmo ie t i e s . Th e f o l lo w in g co mpounds w er e eva lua ted quan -t i t a t ive ly acco r d ing to s t and a r d me thods : G lyce r o l(Renkonen 1962); ste rols (Clark et al. 1968); caro-

tenoids (Liaaen-Jensen and Jensen 1971) ; p las t oqui-none 45 (Lichtenthaler 1968a) . The relat i ve amountso f ~ - toco p her o l an d a lk anes w er e e s t ima ted a f t e rv i s ua l i za t ion on TLC p la t e s w i th e i the r Emmer ie - En -gel reagent (Barr and Crane 1971) or Rhodam in-Tin o-pal reagent (Kleinig and Lempe r t ]97o) . The amountof phytol was determined by GLC.

Elec t r o n M ic r os copy: S amp les o f u l t r a th in s ec t ionsaf ter GA/ OsO 4 or KMnOa f i xat ion as well as of f ro-zenetche d mater i al ( je tals and isolate d globules )f o r TEM w er e p r epa r ed a s d es c r ibed p r ev ious ly ( L ied -

vogel et al . 1976) . Electron microg raphs we re takenwith a Zeiss EM 9 at 6o kV.

Res u l t s

M os t o f th e pe ta l ch r o mo p las t s o f V~o~a t2~ooloP arefound in the basal ( inner) pa r t of epidermal cel ls .The eh r omo p las t s a r e t ig h t ly f i l l ed w i th p la s tog lo -bules (Fig. i ) . The plas t ids of mesoph yll cel ls aremuch less numerous , smaller, and contain thylakoidsas well as some plas togl obules . Oleoso mes are ex-t r emely r a r e in p e ta l ce l l s . F o l low ing f ixa t ion w i thei ther GA/OsO~ or KMnO4, the chromoplas t g lobules

4exh ib i t an e l ec t r on - t r ans lu cen t in t e r io r and a dens esurface lay er 3 to 4 nm thick, corre spond ing to a'half uni t membr ane' (Figs. 1 and 2). Ther e is noind ica t ion o f a t r i l amin a te un i t membr ane . I n f r eeze -f r ac tu r e and f r eeze - e tch p r ep a r a t ions , t he in t e r io ro f the g lobu les l ikew is e app ea r s homogeneous w her easat their surface there is apparent ly a layer of d iffe-r en t f r ac tu r ing p r ope r t i e s w h ich does no t , how ever,corre spond to a typical b io membr ane (Fig. 3) .

A cco r d ing to e l ec t r o n mic r o scopy, i s o la t ed ch r omo-p las t g lobu les w er e f r ee o f r ecogn i s ab le impur i t i e ssuch as cel l organel les , membr anes , or nucleo pro-teins . Presumably, o leosom es are prese nt in the f rac-t ion, a l though in very small amounts ( less than iacco r d ing to mor p homet r i c e s t ima tes o f the ~ n 8~s i tua t io n) . Con tamina t ion b y cu t i cu la r w axes cou ldbe ruled out in three diffe rent ways , e .g . rem oval ofep icu t i l a r w axes w i th ch lo r o f o r m be f o r e t i s s ue homo-genisat ion, search for w ax- s pec i f i c componen t s in

chroma togram s ( there were none detectable ) , andcompar i s on o f th e FA pa t t e r n ( w h ich d i f f e r s g r ea t ly) .

F ig . i: Chromoplas t s , pa cked with plas togl obules , inthe basal c ytopl asm of an epiderma l cel l of a

V~ o~ petal . KMnO 4. 17,ooo:i . Bar, 1 ,um. /

F ig. 2 : F r ac t ion o f i s o la t ed ch r omop la s t g lobu les .OsO4.31,ooo:i . Bar, I /um

F ig . 3 : F r eeze - f r ac tu r e appea r ance o f i s o la t ed ch r o -mopl as t g lobules . 94,ooo:I . Bar, o , I /um.

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Ta b l e I : C h e m i c a l c o m p o s i t i o n of c h r o m o p l a s t gl o b u l e s .D a t a a r e e x p r e s s e d i n p e r c e n t o f t o t a l d r y w e i g h t .

C o n s t i t u e n t s Viola Caltha a

P ro t e i n s 3 . 9 + +P o l a r l i p i d s 4 . 7 7A l k an es 3 . 3 -

Q u i n o n es i . i +S t e ro l s , e s t e r s 0 . 5 +P h y t o l , e s t e r s 2 . 5 -C a ro t e n o i d s , e s t e r s 2 3 1 4Tr i a c y l g l y c e r o l s 5 7 7 4

Sa. 96 95

as i t t e e t a l . (1980)

Ta b l e 2: P o l a r l i p i d c o m p o n e n t s o f p l a s t o g l o b u l e sa n d d i f f e r e n t m e m b r a n e f r a c t i o n s o f p l a s t i d s .

P o l a r l i p i d s I I I I I I IV V

M o n o g a l a c t o s y l d i a c y l g l y c e r o l 3 5 . 1 5 5 . 8 2 8 . 8 3 8 . 4 3 9 . 1D i g a l a c t o s y l d i a c y l g l y c e r o l 2 1 ,1 1 7 , 2 2 6 . 6 3 2 . 3 2 0 .1S u l fo l i p i d 7 , 5 3 . 9 5 , 6 9 . 8 7 . 3P h o s p h o l i p i d s 2 1 . 5 2 3 , 1 3 9 . 0 1 9 . 5 2 6 , 7F ree FA s 1 4 , 5

Sa. 1OO 1OO iOO i00 93 .1

I = C h r o m o p l a s t g l o b u l e s o f Viola tricolor

I I = C h r o m o p l a s t i n t e r n a l m e m b r a n e s o f Narcissuspseudonarcissus (Liedv ogel e t a l . 1976)

I I I : C h l o r o p l a s t e n v e l o p e m e m b r a n e s o f Narcissuspseudonarcissus (Lied vogel e t a l. 1976)

I V = C h l o r o p l a s t t h y l a k o i d m e m b r a n e s o f Narcissuspseudo~rc issus (Liedv ogel e t a l. 1976)

V : C h l o r o p l a s t t h y l a k o i d m e m b r a n e s o f Spin~ciaoleracea (H as h i m o t o an d M u ra k am i 1 9 7 5)

T h e r e s u l t s o f c h r o m o p l a s t g l o b u l e a n a l y s i s a r e s h o w ni n Tab l e 1 . A m o n g s t t h e p ro t e i n s , t w o s p ec i e s (3 0 O O ~6 8 0 0 0 ) p r e v a i l a c c o r d i n g t o S D S - PA G E . T h e p a t t e r n o fp o l a r l i p i d s s t r i k i n g l y r e s e m b l e s t h a t of d i f f e r e n tp l a s t i d m e m b r a n e s ( cf . Ta b l e 2 ). P h o s p h a t i d y l i n o s i t o lh a s b e e n f o u n d i n t r a c e s o n ly, p h o s p h a t i d y l e t h a n o l -a m i n e i s v i r t u a l l y a b s e n t . - A c c o r d i n g t o L i c h t e n -t h a l e r ( 1 9 6 8a ) , 5 q u i n o n e s p ec i e s can b e fo u n d i np e t a l s o f Viola tricolor n a m e l y p l a s t o q u i n o n e 4 5 ,p l a s t o h y d r o q u i n o n e 4 5 , ~ - t o c o p h e r o l , ~ - t o c o q u i n o n e ,a n d v i t a m i n K I . I n i s o l a t e d c h r o m o p l a s t g l o b u l e s , w ec o u l d d e t e c t t w o o f t h e m i n a p p r e c i a b l e a m o u n t s ,( e - t o c o p h e ro l a n d p l a s t o q u i n o n e 4 5, m a s s r a t i o 2 . 2

t o 1 ) . - T h e FA p a t t e rn i s co m p l ex (Tab l e 3 ) . I n ad d i -t i o n t o c o m m o n l y o c c u r i n g FA s , 8 - h y d r o x y s p e c i e s h a v eb e e n f o u n d i n a p p r e c i a b l e a m o u n t s ( m as s p r o p o r t i o n2 : 1 , H an s m an n an d K l e i n i g 1 9 8 2 ) .

Tab l e 3 : F a t t y ac i d (FA ) co m p o s i t i o n ( ) o f t o t a lp l a s t o g l o b u l e l i p i d s f r o m Viola tricolor.

FA s R e g u l a r FA s 8 - h y d r o x y FA s

3

12:0 3 .1 1109:1 1,9 -:2 9.9 -

1 4 : O 7 °0 1 9 . 8

:1 4,4 -:2 25 .2 -

16:O 7 ,9 1 .3:I + -: 2 1 . 2 -

18:O -:i

:2 1 . 8 -:3 4.6 -

Sa. 1OO

T h e m e a n FA m o l . w e i g h t i s 2 3 5 . FAs c o n s t i t u t e 6 3 o ft h e c h r o m o p l a s t g l o b u l e d r y w e i g h t ; L e s s t h a n 1 o ft h e FA s h av e b ee n fo u n d i n f r ee fo rm . - 9 4 o f t h ec a r o t e n o i d s a r e x a n t h o p h y l l e s t e r s . A f t e r s a p o n i f i c a -t i o n, 4 p r i n c i p a l c a r o t e n o i d s ( N e o x a n t h i n 4 , Vi o l a -x a n t h i n 7 2 , L u t e i n e p o x i d e 1 3 , L u t e i n 7 ) a n d s o m em i n o r c o m p o n e n t s c a n b e d e t e c t e d . T h e p a t t e r n o f f a t t ya c i d e s t e r s o f t h e x a n t h o p h y l l s i s r e p o r t e d e l s e w h e r e(H an s m an an d K l e i n i g 19 8 2 ) .

D i s c u s s i o n

I n c h l o r o p l a s t g l o b u l e s p r o t e i n s , s q u a l e n e , s t e r ol sa n d t h e i r e s t e r s , p l a s t i d q u i n o n e s , g l y c o l i p i d s , a n dt r a c e s o f 8 - c a r o t e n e h a v e b e e n f o u nd , b u t n o c h l o r o -p h y l l s n o r x a n t h o p h y l l s o r t h e i r e s t e r s ( G r e e n wo o d e ta l . 1 9 6 3; B a i l e y a n d W h y b o r n 1 9 63 ; L i c h t e n t h a l e r a n dS p r e y 1 9 6 6 ) . I n c h r o m o p l a s t g l o b u l e s , s o m e a d d i t i o n a lc l a s s e s o f c o m p o u n d s h a v e b e e n d e t e c t e d ( L i c h t e n t h a l e r1 9 7 0 ; Wu t t k e 1 9 7 7 ; s ee a l s o S i t t e e t a l . 1 9 8 0 ) , e . g .c a r o t e n o i d s , p h o s p h o l i p i d s , s u l f o l i p i d s , f r e e FA s a n da c y l a t e d g l y c e r o l s . I n t h e p r e s e n t s t u dy, t h e s e r e -s u l t s h a v e b e e n l a rg e l y c o n f i rm e d . Tr i a c a l g l y c e r o l s h a v eb e e n e s t a b l i s h e d a s t h e m a i n c o n s t i t u e n t o f c h r o m o p l a s tg l o b u l e s o f t h e p a n s y, f o l l o w e d b y c a r o t e n o i ds . A d d i -t i o n a l t o t h e c o m p o u n d c l a s s e s g e n e r a l l y f o u n d i np l a s t o g l e b u l e s , a l k a n e s a n d p h y t y l e s t e r s h av e b e e nd i s c o v e r e d i n t h e c h r o m o p l a s t g l o b u l e s o f Vibla. A I -k a n e s h a v e b e e n d e t e c t e d i n c h l o r o p l a s t s b y G 0 1 z ( 1 96 8 ).S t e ff e n s e t a l. ( 1 97 6 ) h av e s h o w n t h a t p h y t o l i s n o tn e c e s s a r i l y e s t e r i f i e d w i t h c h l o r o p h y l l i d e s i n s e e d s .C s u p o r ( 19 70 ) d e m o n s t r a t e d t h e p r e s e n c e o f p h y t y le s t e r s o f l i n o l e n i c a c i d i n g e r o n t o p l a s t s o f A c e rp l a t a n o i d e s .

T h e a p o l a r c o m p o u n d s o f t h e p l a s t o g l o b u l e s r e p r e s e n t av e r y h e t e r o g e n e o u s m i x t u r e. A s t h e a c y l r e s i d u e s b e -

l o n g l a rg e l y t o s h o r t - c h a i n e d a n d u n s a t u r a t e d FA s , i tap p ea r s l i k e l y t h a t t h i s m i x t u re i s i n a f l u i d s t a t e .T h i s a s s u m p t i o n i s b o r n e o u t b y t h e a m o r p h o u s a p p e a r a n -ce o n t h e i n t e r i o r o f t h e g l o b u l e a s s een i n t h e E M ,a s w e l l . a s b y t h e s p h e r i c a l s h a p e o f p l a s t o g l o b u l e sa n d t h e i r a b i l i t y t o b e c o m e d e f o r m e d u n d e r e x o g e n o u sp res s u re ( c f. , e . g . , S i t t e 1 9 6 3 ; T h o m s o n an d P l a t t1 9 7 3) . O n t h e b a s i s o f p h y s i c o - c h e m i c a l c o n s i d e r a t i o n s ,S i t t e ( 19 7 7) an d Wu t t k e (19 7 7) h av e p ro p o s ed t h a t t h ea p o l a r c o m p o n e n t s a r e b u r i e d i n t h e i n t e r i o r o f t h ep l a s t o g l o b u l e s , a n d a r e c o v e r e d b y p o l a r l i p i d s a n dp r o t e i n s a t t h e s u r f a c e o f t h e g l ob u l e . S u c h a n a r r a n g e -m e n t c o u l d a c c o u n t f o r a m a x i m u m o f e n t r o p i c i n t e r -ac t i o n s (Tan fo rd 1 9 78 ) a s w e l l a s fo r t h e l i m i t ed m i s -c i b i l i t y o f a p o l a r a n d a m p h i p o l a r l i p i d s ( S ma l l 1 9 70 ) .

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